| Year |
Citation |
Score |
| 2021 |
Smolders S, Philtjens S, Crosiers D, Sieben A, Hens E, Heeman B, Van Mossevelde S, Pals P, Asselbergh B, Dos Santos Dias R, Vermeiren Y, Vandenberghe R, Engelborghs S, De Deyn PP, Martin JJ, et al. Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease. Acta Neuropathologica Communications. 9: 25. PMID 33579389 DOI: 10.1186/s40478-021-01121-w |
0.324 |
|
| 2018 |
Eidhof I, Baets J, Kamsteeg EJ, Deconinck T, van Ninhuijs L, Martin JJ, Schüle R, Züchner S, De Jonghe P, Schenck A, van de Warrenburg BP. GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia. Brain : a Journal of Neurology. PMID 30084953 DOI: 10.1093/Brain/Awy198 |
0.308 |
|
| 2018 |
Sieben A, Van Mossevelde S, Wauters E, Engelborghs S, van der Zee J, Van Langenhove T, Santens P, Praet M, Boon P, Miatton M, Van Hoecke S, Vandenbulcke M, Vandenberghe R, Cras P, Cruts M, ... ... Martin JJ, et al. Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family. Alzheimer's Research & Therapy. 10: 7. PMID 29370838 DOI: 10.1186/S13195-017-0334-Y |
0.3 |
|
| 2016 |
Van den Bossche T, Sleegers K, Cuyvers E, Engelborghs S, Sieben A, De Roeck A, Van Cauwenberghe C, Vermeulen S, Van den Broeck M, Laureys A, Peeters K, Mattheijssens M, Vandenbulcke M, Vandenberghe R, Martin JJ, et al. Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation. Neurology. PMID 27037232 DOI: 10.1212/Wnl.0000000000002628 |
0.336 |
|
| 2014 |
Semmler AL, Sacconi S, Bach JE, Liebe C, Bürmann J, Kley RA, Ferbert A, Anderheiden R, Van den Bergh P, Martin JJ, De Jonghe P, Neuen-Jacob E, Müller O, Deschauer M, Bergmann M, et al. Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies. Orphanet Journal of Rare Diseases. 9: 121. PMID 25208129 DOI: 10.1186/s13023-014-0121-9 |
0.348 |
|
| 2014 |
van der Zee J, Van Langenhove T, Kovacs GG, Dillen L, Deschamps W, Engelborghs S, Mat?j R, Vandenbulcke M, Sieben A, Dermaut B, Smets K, Van Damme P, Merlin C, Laureys A, Van Den Broeck M, ... ... Martin JJ, et al. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathologica. 128: 397-410. PMID 24899140 DOI: 10.1007/S00401-014-1298-7 |
0.304 |
|
| 2013 |
Dohrn MF, Röcken C, De Bleecker JL, Martin JJ, Vorgerd M, Van den Bergh PY, Ferbert A, Hinderhofer K, Schröder JM, Weis J, Schulz JB, Claeys KG. Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy. Journal of Neurology. 260: 3093-108. PMID 24101130 DOI: 10.1007/s00415-013-7124-7 |
0.315 |
|
| 2013 |
Van Langenhove T, van der Zee J, Gijselinck I, Engelborghs S, Vandenberghe R, Vandenbulcke M, De Bleecker J, Sieben A, Versijpt J, Ivanoiu A, Deryck O, Willems C, Dillen L, Philtjens S, Maes G, ... ... Martin JJ, et al. Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort. Jama Neurology. 70: 365-73. PMID 23338682 DOI: 10.1001/2013.Jamaneurol.181 |
0.339 |
|
| 2012 |
Scalais E, Francois B, Schlesser P, Stevens R, Nuttin C, Martin JJ, Van Coster R, Seneca S, Roels F, Van Goethem G, Löfgren A, De Meirleir L. Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 16: 542-8. PMID 22342071 DOI: 10.1016/j.ejpn.2012.01.013 |
0.678 |
|
| 2009 |
van der Zee J, Pirici D, Van Langenhove T, Engelborghs S, Vandenberghe R, Hoffmann M, Pusswald G, Van den Broeck M, Peeters K, Mattheijssens M, Martin JJ, De Deyn PP, Cruts M, Haubenberger D, Kumar-Singh S, et al. Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. Neurology. 73: 626-32. PMID 19704082 DOI: 10.1212/Wnl.0B013E3181B389D9 |
0.375 |
|
| 2009 |
Roels F, Verloo P, Eyskens F, François B, Seneca S, De Paepe B, Martin JJ, Meersschaut V, Praet M, Scalais E, Espeel M, Smet J, Van Goethem G, Van Coster R. Mitochondrial mosaics in the liver of 3 infants with mtDNA defects. Bmc Clinical Pathology. 9: 4. PMID 19500334 DOI: 10.1186/1472-6890-9-4 |
0.659 |
|
| 2008 |
Brouwers N, Sleegers K, Engelborghs S, Maurer-Stroh S, Gijselinck I, van der Zee J, Pickut BA, Van den Broeck M, Mattheijssens M, Peeters K, Schymkowitz J, Rousseau F, Martin JJ, Cruts M, De Deyn PP, et al. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology. 71: 656-64. PMID 18565828 DOI: 10.1212/01.Wnl.0000319688.89790.7A |
0.335 |
|
| 2008 |
Monnier N, Marty I, Faure J, Castiglioni C, Desnuelle C, Sacconi S, Estournet B, Ferreiro A, Romero N, Laquerriere A, Lazaro L, Martin JJ, Morava E, Rossi A, Van der Kooi A, et al. Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. Human Mutation. 29: 670-8. PMID 18253926 DOI: 10.1002/humu.20696 |
0.332 |
|
| 2007 |
Scalais E, Nuttin C, Seneca S, Smet J, Paepe BD, Martin J-, Stevens R, Pierart F, Battisti O, Lissens W, Meirleir LD, Coster RV. Infantile presentation of the mitochondrial A8344G mutation. European Journal of Neurology. 14: 3-5. PMID 17956438 DOI: 10.1111/J.1468-1331.2007.01926.X |
0.425 |
|
| 2007 |
Paepe BD, Smet J, Lammens M, Seneca S, Martin J, Bleecker JD, Coster RV. M.P.1.01 Immunohistochemical studies of oxidative phosphorylation in skeletal muscle of patients with mitochondrial tRNA gene mutations Neuromuscular Disorders. 17: 767-768. DOI: 10.1016/J.Nmd.2007.06.026 |
0.39 |
|
| 2006 |
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature. 442: 920-4. PMID 16862115 DOI: 10.1038/Nature05017 |
0.309 |
|
| 2006 |
van der Zee J, Rademakers R, Engelborghs S, Gijselinck I, Bogaerts V, Vandenberghe R, Santens P, Caekebeke J, De Pooter T, Peeters K, Lübke U, Van den Broeck M, Martin JJ, Cruts M, De Deyn PP, et al. A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. Brain : a Journal of Neurology. 129: 841-52. PMID 16495329 DOI: 10.1093/Brain/Awl029 |
0.309 |
|
| 2005 |
Bitoun M, Maugenre S, Jeannet P, Lacène E, Ferrer X, Laforêt P, Martin J, Laporte J, Lochmüller H, Beggs AH, Fardeau M, Eymard B, Romero NB, Guicheney P. Mutations in dynamin 2 cause dominant centronuclear myopathy Nature Genetics. 37: 1207-1209. PMID 16227997 DOI: 10.1038/Ng1657 |
0.303 |
|
| 2005 |
Laing NG, Ceuterick-de Groote C, Dye DE, Liyanage K, Duff RM, Dubois B, Robberecht W, Sciot R, Martin JJ, Goebel HH. Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases. Neurology. 64: 527-9. PMID 15699387 DOI: 10.1212/01.Wnl.0000150581.37514.30 |
0.378 |
|
| 2004 |
Van Goethem G, Luoma P, Rantamäki M, Al Memar A, Kaakkola S, Hackman P, Krahe R, Löfgren A, Martin JJ, De Jonghe P, Suomalainen A, Udd B, Van Broeckhoven C. POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. Neurology. 63: 1251-7. PMID 15477547 DOI: 10.1212/01.Wnl.0000140494.58732.83 |
0.401 |
|
| 2004 |
Dermaut B, Kumar-Singh S, Engelborghs S, Theuns J, Rademakers R, Saerens J, Pickut BA, Peeters K, van den Broeck M, Vennekens K, Claes S, Cruts M, Cras P, Martin JJ, Van Broeckhoven C, et al. A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques. Annals of Neurology. 55: 617-26. PMID 15122701 DOI: 10.1002/Ana.20083 |
0.321 |
|
| 2004 |
Michalik A, Martin J-, Broeckhoven CV. Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy. European Journal of Human Genetics. 12: 2-15. PMID 14571264 DOI: 10.1038/Sj.Ejhg.5201108 |
0.356 |
|
| 2003 |
Van Goethem G, Mercelis R, Löfgren A, Seneca S, Ceuterick C, Martin JJ, Van Broeckhoven C. Patient homozygous for a recessive POLG mutation presents with features of MERRF. Neurology. 61: 1811-3. PMID 14694057 |
0.371 |
|
| 2003 |
Van Goethem G, Löfgren A, Dermaut B, Ceuterick C, Martin JJ, Van Broeckhoven C. Digenic progressive external ophthalmoplegia in a sporadic patient: recessive mutations in POLG and C10orf2/Twinkle. Human Mutation. 22: 175-6. PMID 12872260 DOI: 10.1002/Humu.10246 |
0.693 |
|
| 2003 |
Van Goethem G, Martin JJ, Van Broeckhoven C. Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classification. Neuromolecular Medicine. 3: 129-46. PMID 12835509 DOI: 10.1385/NMM:3:3:129 |
0.718 |
|
| 2003 |
Jordanova A, De Jonghe P, Boerkoel CF, Takashima H, De Vriendt E, Ceuterick C, Martin JJ, Butler IJ, Mancias P, Papasozomenos SCh, Terespolsky D, Potocki L, Brown CW, Shy M, Rita DA, et al. Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. 126: 590-7. PMID 12566280 DOI: 10.1093/Brain/Awg059 |
0.33 |
|
| 2003 |
Van Goethem G, Martin JJ, Dermaut B, Löfgren A, Wibail A, Ververken D, Tack P, Dehaene I, Van Zandijcke M, Moonen M, Ceuterick C, De Jonghe P, Van Broeckhoven C. Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. Neuromuscular Disorders : Nmd. 13: 133-42. PMID 12565911 DOI: 10.1016/S0960-8966(02)00216-X |
0.503 |
|
| 2002 |
Takashima H, Boerkoel CF, De Jonghe P, Ceuterick C, Martin JJ, Voit T, Schröder JM, Williams A, Brophy PJ, Timmerman V, Lupski JR. Periaxin mutations cause a broad spectrum of demyelinating neuropathies. Annals of Neurology. 51: 709-15. PMID 12112076 DOI: 10.1002/Ana.10213 |
0.313 |
|
| 2002 |
Van Goethem G, Martin JJ, Van Broeckhoven C. Progressive external ophthalmoplegia and multiple mitochondrial DNA deletions. Acta Neurologica Belgica. 102: 39-42. PMID 12094562 |
0.71 |
|
| 2001 |
Van Goethem G, Dermaut B, Löfgren A, Martin JJ, Van Broeckhoven C. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Nature Genetics. 28: 211-2. PMID 11431686 DOI: 10.1038/90034 |
0.361 |
|
| 2001 |
Ceuterick-de Groote C, De Jonghe P, Timmerman V, Van Goethem G, Löfgren A, Ceulemans B, Van Broeckhoven C, Martin JJ. Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy. Pathology, Research and Practice. 197: 193-8. PMID 11314784 DOI: 10.1078/0344-0338-00033 |
0.384 |
|
| 2001 |
De Jonghe P, Mersivanova I, Nelis E, Favero JD, Martin JJ, Van Broeckhoven C, Evgrafov O, Timmerman V. Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E Annals of Neurology. 49: 245-249. PMID 11220745 DOI: 10.1002/1531-8249(20010201)49:2<245::Aid-Ana45>3.0.Co;2-A |
0.308 |
|
| 1999 |
Martin J-, Martin L, Löfgren A, D’Hooghe M, Storm K, Balemans W, Palau F, Broeckhoven Cv. Classical Friedreich's ataxia and its genotype. European Neurology. 42: 109-115. PMID 10473983 DOI: 10.1159/000069420 |
0.351 |
|
| 1998 |
Mitchison HM, Hofmann SL, Becerra CH, Munroe PB, Lake BD, Crow YJ, Stephenson JB, Williams RE, Hofman IL, Taschner PE, Martin JJ, Philippart M, Andermann E, Andermann F, Mole SE, et al. Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits. Human Molecular Genetics. 7: 291-7. PMID 9425237 DOI: 10.1093/Hmg/7.2.291 |
0.332 |
|
| 1996 |
Timmerman V, De Jonghe P, Spoelders P, Simokovic S, Löfgren A, Nelis E, Vance J, Martin JJ, Van Broeckhoven C. Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13 Neurology. 46: 1311-1318. PMID 8628473 DOI: 10.1212/Wnl.46.5.1311 |
0.353 |
|
| 1994 |
Martin JJ, Krols L, Ceuterick C, Van Broeckhoven C, Van Regemorter N, Hayer-Delatte F, Brucher JM, de Barsy T, Szliwowski H, Evrard P, Tassignon MJ, Smet-Dieleman H, Willems PJ. On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family Acta Neuropathologica. 88: 277-286. PMID 7839819 DOI: 10.1007/Bf00310370 |
0.311 |
|
| 1992 |
Hoogendijk JE, Hensels GW, Janssen EAM, Valentijn LJ, Baas F, Visser Md, Bolhuis PA, Gabreels-Festen AAWM, Gabreels FJM, onghe Pd, Martin J-, Broeckhoven Cv. De-novo mutation in hereditary motor and sensory neuropathy type I. The Lancet. 339: 1081-1082. PMID 1349106 DOI: 10.1016/0140-6736(92)90668-S |
0.385 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2004 |
Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, ... ... Martin JJ, et al. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nature Genetics. 36: 602-6. PMID 15122254 DOI: 10.1038/Ng1354 |
0.3 |
|
| 2007 |
van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Sleegers K, Hannequin D, Dermaut B, Schymkowitz J, Campion D, Santens P, Martin JJ, et al. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Human Mutation. 28: 416. PMID 17345602 DOI: 10.1002/Humu.9484 |
0.299 |
|
| 1992 |
Van Broeckhoven C, Backhovens H, Cruts M, De Winter G, Bruyland M, Cras P, Martin JJ. Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3. Nature Genetics. 2: 335-9. PMID 1303290 DOI: 10.1038/Ng1292-335 |
0.299 |
|
| 1994 |
Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C. Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene Human Genetics. 94: 653-657. PMID 7527371 DOI: 10.1007/Bf00206959 |
0.298 |
|
| 1999 |
Timmerman V, De Jonghe P, Ceuterick C, De Vriendt E, Lofgren A, Nelis E, Warner LE, Lupski JR, Martin JJ, Van Broeckhoven C. Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype Neurology. 52: 1827-1832. PMID 10371530 DOI: 10.1212/Wnl.52.9.1827 |
0.297 |
|
| 2017 |
Van den Bossche T, De Roeck A, Sieben A, Martin J, Vandenberghe R, Engelborghs S, De Deyn PP, Sleegers K, Cras P, Van Broeckhoven C. CONTRIBUTION OF RARE DELETERIOUS ABCA7 MUTATIONS TO A BELGIAN EARLY-ONSET ALZHEIMER’S DISEASE COHORT Alzheimer's & Dementia. 13: P573-P574. DOI: 10.1016/J.Jalz.2017.07.191 |
0.294 |
|
| 2002 |
Pou Serradell A, Monells J, Téllez MJ, Fossas P, Löfgren A, Meuleman J, Timmerman V, De Jonghe P, Ceuterick C, Martin JJ. Hereditary neuropathy with liability to pressure palsies: Study of six Spanish families Revue Neurologique. 158: 579-588. PMID 12072826 |
0.292 |
|
| 1996 |
Meire FM, Van Coster R, Cochaux P, Obermaier-Kusser B, Candaele C, Martin JJ. Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations. Ophthalmic Genetics. 16: 119-26. PMID 8556281 DOI: 10.3109/13816819509059971 |
0.291 |
|
| 2009 |
Zecic A, Smet JE, De Praeter CM, Vanhaesebrouck P, Viscomi C, Van Den Broecke C, De Paepe B, Lohse P, Martin JJ, Jackson JG, Campbell CR, De Meirleir LJ, Zeviani M, Seneca SH, Lissens W, et al. Lactic acidosis in a newborn with adrenal calcifications. Pediatric Research. 66: 317-22. PMID 19581830 DOI: 10.1203/Pdr.0B013E3181B40A80 |
0.291 |
|
| 1993 |
Palau F, Löfgren A, Jonghe PD, Bort S, Nelis E, Sevilla T, Martin JJ, Vilchez J, Prieto F, Broeckhoven CV. Origin of the de novo duplication in charcot - marie - tooth disease type 1A: Unequal nonsister chromatid exchange during spermatogenesis Human Molecular Genetics. 2: 2031-2035. PMID 8111370 DOI: 10.1093/hmg/2.12.2031 |
0.29 |
|
| 1997 |
Monsieurs KG, Van Broeckhoven C, Martin JJ, Dehaene I, Heytens LG. Malignant hyperthermia susceptibility in a patient with concomitant motor neuron disease. Journal of the Neurological Sciences. 142: 36-8. PMID 8902717 DOI: 10.1016/0022-510x(96)00034-2 |
0.289 |
|
| 1995 |
Benomar A, Krols L, Stevanin G, Cancel G, LeGuern E, David G, Ouhabi H, Martin J-, Dürr A, Zaim A, Ravisé N, Busque C, Penet C, Regemorter NV, Weissenbach J, et al. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. Nature Genetics. 10: 84-88. PMID 7647798 DOI: 10.1038/Ng0595-84 |
0.288 |
|
| 2004 |
Verhoeven K, Coen K, De Vriendt E, Jacobs A, Van Gerwen V, Smouts I, Pou-Serradell A, Martin JJ, Timmerman V, De Jonghe P. SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I. Neurology. 62: 1001-2. PMID 15037712 DOI: 10.1212/01.Wnl.0000115388.10828.5C |
0.286 |
|
| 2018 |
Wauters E, Van Mossevelde S, Sleegers K, van der Zee J, Engelborghs S, Sieben A, Vandenberghe R, Philtjens S, Van den Broeck M, Peeters K, Cuijt I, De Coster W, Van Langenhove T, Santens P, Ivanoiu A, ... ... Martin JJ, et al. Clinical variability and onset age modifiers in an extended Belgian GRN founder family. Neurobiology of Aging. 67: 84-94. PMID 29653316 DOI: 10.1016/J.Neurobiolaging.2018.03.007 |
0.284 |
|
| 2009 |
De Paepe B, Smet J, Lammens M, Seneca S, Martin JJ, De Bleecker J, De Meirleir L, Lissens W, Van Coster R. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects. Journal of Clinical Pathology. 62: 172-6. PMID 19181635 DOI: 10.1136/jcp.2008.061267 |
0.283 |
|
| 1997 |
Nelis E, Simokovic S, Timmerman V, Löfgren A, Backhovens H, De Jonghe P, Martin JJ, Van Broeckhoven C. Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-tooth neuropathy type 1: Identification of five new mutations Human Mutation. 9: 47-52. PMID 8990008 DOI: 10.1002/(Sici)1098-1004(1997)9:1<47::Aid-Humu8>3.0.Co;2-M |
0.282 |
|
| 2001 |
Meuleman J, Pou-Serradell A, Löfgren A, Ceuterick C, Martin JJ, Timmerman V, Van Broeckhoven C, De Jonghe P. A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies. Neuromuscular Disorders : Nmd. 11: 400-3. PMID 11369192 DOI: 10.1016/S0960-8966(00)00214-5 |
0.281 |
|
| 2002 |
Ferreiro A, Quijano-Roy S, Pichereau C, Moghadaszadeh B, Goemans N, Bönnemann C, Jungbluth H, Straub V, Villanova M, Leroy JP, Romero NB, Martin JJ, Muntoni F, Voit T, Estournet B, et al. Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies. American Journal of Human Genetics. 71: 739-49. PMID 12192640 DOI: 10.1086/342719 |
0.279 |
|
| 2014 |
Smets K, Deconinck T, Baets J, Sieben A, Martin JJ, Smouts I, Wang S, Taroni F, Di Bella D, Van Hecke W, Parizel PM, Jadoul C, De Potter R, Couvreur F, Rugarli E, et al. Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28. Neurology. 82: 2092-100. PMID 24814845 DOI: 10.1212/Wnl.0000000000000491 |
0.279 |
|
| 1998 |
Monsieurs KG, Van Broeckhoven C, Martin JJ, Van Hoof VO, Heytens L. Gly341Arg mutation indicating malignant hyperthermia susceptibility: specific cause of chronically elevated serum creatine kinase activity. Journal of the Neurological Sciences. 154: 62-5. PMID 9543323 DOI: 10.1016/s0022-510x(97)00215-3 |
0.278 |
|
| 2007 |
Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, ... ... Martin JJ, et al. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Archives of Neurology. 64: 1436-46. PMID 17923627 DOI: 10.1001/Archneur.64.10.1436 |
0.277 |
|
| 1999 |
De Jonghe P, Nelis E, Timmerman V, Löfgren A, Martin JJ, VAN Broeckhoven C. Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and Results. Annals of the New York Academy of Sciences. 883: 389-396. PMID 29086951 DOI: 10.1111/J.1749-6632.1999.Tb08600.X |
0.277 |
|
| 1999 |
De Jonghe P, Nelis E, Timmerman V, Löfgren A, Martin JJ, Van Broeckhoven C. Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders: Approaches and results Annals of the New York Academy of Sciences. 883: 389-396. PMID 10586263 |
0.277 |
|
| 2000 |
van Goethem G, Löfgren A, Martin JJ, van Broeckhoven C. Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA. Journal of Medical Genetics. 37: 547-8. PMID 10970191 |
0.276 |
|
| 2016 |
Perrone F, Nguyen HP, Van Mossevelde S, Moisse M, Sieben A, Santens P, De Bleecker J, Vandenbulcke M, Engelborghs S, Baets J, Cras P, Vandenberghe R, De Jonghe P, De Deyn PP, Martin JJ, et al. Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients. Neurobiology of Aging. PMID 28069311 DOI: 10.1016/J.Neurobiolaging.2016.12.008 |
0.275 |
|
| 2015 |
Gijselinck I, Van Mossevelde S, van der Zee J, Sieben A, Engelborghs S, De Bleecker J, Ivanoiu A, Deryck O, Edbauer D, Zhang M, Heeman B, Bäumer V, Van den Broeck M, Mattheijssens M, Peeters K, ... ... Martin JJ, et al. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter. Molecular Psychiatry. PMID 26481318 DOI: 10.1038/Mp.2015.159 |
0.271 |
|
| 1999 |
De Jonghe C, Cras P, Vanderstichele H, Cruts M, Vanderhoeven I, Smouts I, Vanmechelen E, Martin JJ, Hendriks L, Van Broeckhoven C. Evidence that Abeta42 plasma levels in presenilin-1 mutation carriers do not allow for prediction of their clinical phenotype. Neurobiology of Disease. 6: 280-7. PMID 10448055 DOI: 10.1006/nbdi.1999.0247 |
0.267 |
|
| 1994 |
Nelis E, Timmerman V, De Jonghe P, Muylle L, Martin JJ, Van Broeckhoven C. Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B. Journal of Medical Genetics. 31: 811-5. PMID 7530774 DOI: 10.1136/Jmg.31.10.811 |
0.267 |
|
| 1992 |
Hendriks L, van Duijn CM, Cras P, Cruts M, Van Hul W, van Harskamp F, Warren A, McInnis MG, Antonarakis SE, Martin JJ. Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene. Nature Genetics. 1: 218-21. PMID 1303239 DOI: 10.1038/Ng0692-218 |
0.266 |
|
| 2003 |
Ammar N, Nelis E, Merlini L, Barisić N, Amouri R, Ceuterick C, Martin JJ, Timmerman V, Hentati F, De Jonghe P. Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. Neuromuscular Disorders : Nmd. 13: 720-8. PMID 14561495 DOI: 10.1016/S0960-8966(03)00093-2 |
0.265 |
|
| 1998 |
Cras P, van Harskamp F, Hendriks L, Ceuterick C, van Duijn CM, Stefanko SZ, Hofman A, Kros JM, Van Broeckhoven C, Martin JJ. Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutation. Acta Neuropathologica. 96: 253-60. PMID 9754958 DOI: 10.1007/s004010050892 |
0.265 |
|
| 1999 |
De Jonghe P, Timmerman V, Ceuterick C, Nelis E, De Vriendt E, Löfgren A, Vercruyssen A, Verellen C, Van Maldergem L, Martin JJ, Van Broeckhoven C. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype Brain. 122: 281-290. PMID 10071056 DOI: 10.1093/Brain/122.2.281 |
0.265 |
|
| 2000 |
Houlden H, Baker M, McGowan E, Lewis P, Hutton M, Crook R, Wood NW, Kumar-Singh S, Geddes J, Swash M, Scaravilli F, Holton JL, Lashley T, Tomita T, Hashimoto T, ... ... Martin JJ, et al. Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. Annals of Neurology. 48: 806-8. PMID 11079548 DOI: 10.1002/1531-8249(200011)48:5<806::Aid-Ana18>3.0.Co;2-F |
0.262 |
|
| 2015 |
Van Mossevelde S, van der Zee J, Gijselinck I, Engelborghs S, Sieben A, Van Langenhove T, De Bleecker J, Baets J, Vandenbulcke M, Van Laere K, Ceyssens S, Van den Broeck M, Peeters K, Mattheijssens M, Cras P, ... ... Martin JJ, et al. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort. Brain : a Journal of Neurology. PMID 26674655 DOI: 10.1093/Brain/Awv358 |
0.261 |
|
| 2002 |
Van Everbroeck B, Green AJ, Vanmechelen E, Vanderstichele H, Pals P, Sanchez-Valle R, Corrales NC, Martin JJ, Cras P. Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 73: 79-81. PMID 12082054 DOI: 10.1136/Jnnp.73.1.79 |
0.26 |
|
| 1997 |
Okochi M, Ishii K, Usami M, Sahara N, Kametani F, Tanaka K, Fraser PE, Ikeda M, Saunders AM, Hendriks L, Shoji SI, Nee LE, Martin JJ, Van Broeckhoven C, St George-Hyslop PH, et al. Proteolytic processing of presenilin-1 (PS-1) is not associated with Alzheimer's disease with or without PS-1 mutations. Febs Letters. 418: 162-6. PMID 9414118 DOI: 10.1016/S0014-5793(97)01378-1 |
0.258 |
|
| 2013 |
Martin E, Schüle R, Smets K, Rastetter A, Boukhris A, Loureiro JL, Gonzalez MA, Mundwiller E, Deconinck T, Wessner M, Jornea L, Oteyza AC, Durr A, Martin JJ, Schöls L, et al. Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. American Journal of Human Genetics. 92: 238-44. PMID 23332916 DOI: 10.1016/J.Ajhg.2012.11.021 |
0.257 |
|
| 1995 |
Cruts M, Backhovens H, Theuns J, Clark RF, Le Paslier D, Weissenbach J, Goate AM, Martin JJ, Van Broeckhoven C. Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3. Human Molecular Genetics. 4: 1355-64. PMID 7581374 DOI: 10.1093/Hmg/4.8.1355 |
0.256 |
|
| 2014 |
Kleinberger G, Yamanishi Y, Suárez-Calvet M, Czirr E, Lohmann E, Cuyvers E, Struyfs H, Pettkus N, Wenninger-Weinzierl A, Mazaheri F, Tahirovic S, Lleó A, Alcolea D, Fortea J, Willem M, ... ... Martin JJ, et al. TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. Science Translational Medicine. 6: 243ra86. PMID 24990881 DOI: 10.1126/Scitranslmed.3009093 |
0.254 |
|
| 2016 |
Denora PS, Smets K, Zolfanelli F, Ceuterick-de Groote C, Casali C, Deconinck T, Sieben A, Gonzales M, Zuchner S, Darios F, Peeters D, Brice A, Malandrini A, De Jonghe P, Santorelli FM, ... ... Martin JJ, et al. Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions. Brain : a Journal of Neurology. PMID 27016404 DOI: 10.1093/Brain/Aww061 |
0.253 |
|
| 2005 |
Wuyts W, Reyniers E, Ceuterick C, Storm K, de Barsy T, Martin JJ. Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene. American Journal of Medical Genetics. Part A. 82-4. PMID 15637709 DOI: 10.1002/ajmg.a.30517 |
0.253 |
|
| 1999 |
Vanderhoeven I, Cras P, Martin JJ, Van Broeckhoven C, De Jonghe C. Proteolytic processing of presenilin-1 in human lymphoblasts is not affected by the presence of the I143T and G384A mutations. Neuroscience Letters. 274: 183-6. PMID 10548420 DOI: 10.1016/S0304-3940(99)00722-3 |
0.252 |
|
| 2002 |
Van Everbroeck B, Dewulf E, Pals P, Lübke U, Martin JJ, Cras P. The role of cytokines, astrocytes, microglia and apoptosis in Creutzfeldt-Jakob disease. Neurobiology of Aging. 23: 59-64. PMID 11755020 DOI: 10.1016/S0197-4580(01)00236-6 |
0.252 |
|
| 1999 |
Van Everbroeck B, Pals P, Martin JJ, Cras P. Antigen retrieval in prion protein immunohistochemistry. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 47: 1465-70. PMID 10544219 DOI: 10.1177/002215549904701112 |
0.248 |
|
| 2006 |
Brouwers N, Sleegers K, Engelborghs S, Bogaerts V, Serneels S, Kamali K, Corsmit E, De Leenheir E, Martin JJ, De Deyn PP, Van Broeckhoven C, Theuns J. Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease. Brain : a Journal of Neurology. 129: 2984-91. PMID 16931535 DOI: 10.1093/Brain/Awl212 |
0.247 |
|
| 2012 |
Sieben A, Van Langenhove T, Engelborghs S, Martin JJ, Boon P, Cras P, De Deyn PP, Santens P, Van Broeckhoven C, Cruts M. The genetics and neuropathology of frontotemporal lobar degeneration. Acta Neuropathologica. 124: 353-72. PMID 22890575 DOI: 10.1007/s00401-012-1029-x |
0.247 |
|
| 1998 |
Nelis E, Jonghe PD, Vriendt ED, Patel PI, Martin JJ, Broeckhoven CV. Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP. Journal of Medical Genetics. 35: 590-593. PMID 9678704 DOI: 10.1136/Jmg.35.7.590 |
0.246 |
|
| 2002 |
Martin JJ, Ceuterick C. Neuropathology of some hereditary conditions affecting central and peripheral nervous system. Acta Neurologica Belgica. 102: 30-5. PMID 12094560 |
0.245 |
|
| 2017 |
Van Maldergem L, Besse A, De Paepe B, Blakely EL, Appadurai V, Humble MM, Piard J, Craig K, He L, Hella P, Debray FG, Martin JJ, Gaussen M, Laloux P, Stevanin G, et al. POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism. Annals of Clinical and Translational Neurology. 4: 4-14. PMID 28078310 DOI: 10.1002/acn3.361 |
0.244 |
|
| 1993 |
Abs R, Parizel PM, Willems PJ, Kelft EVD, Verlooy J, Mahler C, Verhelst J, Marck EV, Martin J-. The association of meningioma and pituitary adenoma : report of seven cases and review of the literature European Neurology. 33: 416-422. PMID 8307062 DOI: 10.1159/000116986 |
0.238 |
|
| 2006 |
Van Everbroeck B, Michotte A, Sciot R, Godfraind C, Deprez M, Quoilin S, Martin JJ, Cras P. Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium. European Journal of Epidemiology. 21: 443-7. PMID 16835721 DOI: 10.1007/s10654-006-9012-2 |
0.236 |
|
| 1990 |
Truyen L, Gheuens J, Vyver FLVd, Parizel PM, Peersman GV, Martin J-. Improved correlation of magnetic resonance imaging (MRI) with clinical status in multiple sclerosis (MS) by use of an extensive standardized imaging-protocol. Journal of the Neurological Sciences. 96: 173-182. PMID 2376749 DOI: 10.1016/0022-510X(90)90130-F |
0.236 |
|
| 1987 |
Roodhooft AM, Van Acker KJ, Martin JJ, Ceuterick C, Scholte HR, Luyt-Houwen IE. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase. Neuropediatrics. 17: 221-6. PMID 3027606 DOI: 10.1055/s-2008-1052534 |
0.232 |
|
| 1996 |
Volder ID, Truyen L, Goethem JV, Vercruyssen A, Martin J-. Tuberculous meningitis in immunocompetent adults: two cases with a clinico-radiological discussion Clinical Neurology and Neurosurgery. 98: 312-317. PMID 8930422 DOI: 10.1016/0303-8467(96)00046-7 |
0.232 |
|
| 2012 |
Gijselinck I, Van Langenhove T, van der Zee J, Sleegers K, Philtjens S, Kleinberger G, Janssens J, Bettens K, Van Cauwenberghe C, Pereson S, Engelborghs S, Sieben A, De Jonghe P, Vandenberghe R, Santens P, ... ... Martin JJ, et al. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study. The Lancet. Neurology. 11: 54-65. PMID 22154785 DOI: 10.1016/S1474-4422(11)70261-7 |
0.231 |
|
| 2002 |
Hoyaux D, Boom A, Van den Bosch L, Belot N, Martin JJ, Heizmann CW, Kiss R, Pochet R. S100A6 overexpression within astrocytes associated with impaired axons from both ALS mouse model and human patients. Journal of Neuropathology and Experimental Neurology. 61: 736-44. PMID 12152788 DOI: 10.1093/jnen/61.8.736 |
0.231 |
|
| 1997 |
De Jonghe P, Timmerman V, Nelis E, Martin JJ, Van Broeckhoven C. Charcot-Marie-Tooth disease and related peripheral neuropathies Journal of the Peripheral Nervous System. 2: 370-387. PMID 10975746 |
0.229 |
|
| 2014 |
Van den Bergh PY, Martin JJ, Lecouvet F, Udd B, Schmedding E. Laing early-onset distal myopathy in a Belgian family. Acta Neurologica Belgica. 114: 253-6. PMID 24710723 DOI: 10.1007/s13760-014-0298-7 |
0.228 |
|
| 1996 |
Varley JM, McGown G, Thorncroft M, Tricker KJ, Teare MD, Santibanez-Koref MF, Martin J, Birch JM, Evans DG. An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53. Journal of Medical Genetics. 32: 942-5. PMID 8825920 DOI: 10.1136/jmg.32.12.942 |
0.226 |
|
| 1991 |
Chartier-Harlin MC, Crawford F, Hamandi K, Mullan M, Goate A, Hardy J, Backhovens H, Martin JJ, Broeckhoven CV. Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease. Neuroscience Letters. 129: 134-5. PMID 1922963 DOI: 10.1016/0304-3940(91)90738-F |
0.226 |
|
| 2014 |
Götzl JK, Mori K, Damme M, Fellerer K, Tahirovic S, Kleinberger G, Janssens J, van der Zee J, Lang CM, Kremmer E, Martin JJ, Engelborghs S, Kretzschmar HA, Arzberger T, Van Broeckhoven C, et al. Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis. Acta Neuropathologica. 127: 845-60. PMID 24619111 DOI: 10.1007/S00401-014-1262-6 |
0.224 |
|
| 1976 |
Marin L, Martin JJ, Ceuterick C. [Infantile form of Hallervorden-Spatz disease (author's transl)]. Acta Neurologica Belgica. 75: 257-66. PMID 1220521 |
0.222 |
|
| 2014 |
Debette S, Goeggel Simonetti B, Schilling S, Martin JJ, Kloss M, Sarikaya H, Hausser I, Engelter S, Metso TM, Pezzini A, Thijs V, Touzé E, Paolucci S, Costa P, Sessa M, et al. Familial occurrence and heritable connective tissue disorders in cervical artery dissection. Neurology. 83: 2023-31. PMID 25355833 DOI: 10.1212/WNL.0000000000001027 |
0.221 |
|
| 2004 |
De Block CE, De Leeuw IH, Maassen JA, Ballaux D, Martin JJ. A novel 7301-bp deletion in mitochondrial DNA in a patient with Kearns-Sayre syndrome, diabetes mellitus, and primary amenorrhoea. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. 112: 80-3. PMID 15031771 DOI: 10.1055/s-2004-815754 |
0.219 |
|
| 2009 |
Gijselinck I, Sleegers K, Engelborghs S, Robberecht W, Martin JJ, Vandenberghe R, Sciot R, Dermaut B, Goossens D, van der Zee J, De Pooter T, Del-Favero J, Santens P, De Jonghe P, De Deyn PP, et al. Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Neurobiology of Aging. 30: 1329-31. PMID 18068872 DOI: 10.1016/J.Neurobiolaging.2007.11.002 |
0.218 |
|
| 1999 |
Timmerman V, Beuten J, Irobi J, De Jonghe P, Martin JJ, VAN Broeckhoven C. Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics. Annals of the New York Academy of Sciences. 883: 60-64. PMID 29086966 DOI: 10.1111/J.1749-6632.1999.Tb08568.X |
0.218 |
|
| 1999 |
Timmerman V, Beuten J, Irobi J, De Jonghe P, Martin JJ, Van Broeckhoven C. Distal hereditary motor neuropathy type II (distal HMN type II): Phenotype and molecular genetics Annals of the New York Academy of Sciences. 883: 60-64. PMID 10586231 |
0.218 |
|
| 2015 |
Janssens J, Philtjens S, Kleinberger G, Van Mossevelde S, van der Zee J, Cacace R, Engelborghs S, Sieben A, Banzhaf-Strathmann J, Dillen L, Merlin C, Cuijt I, Robberecht C, Schmid B, Santens P, ... ... Martin JJ, et al. Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains. Acta Neuropathologica Communications. 3: 68. PMID 26555887 DOI: 10.1186/S40478-015-0246-7 |
0.217 |
|
| 1999 |
Reyniers E, Martin JJ, Cras P, Van Marck E, Handig I, Jorens HZ, Oostra BA, Kooy RF, Willems PJ. Postmortem examination of two fragile X brothers with an FMR1 full mutation. American Journal of Medical Genetics. 84: 245-9. PMID 10331601 DOI: 10.1002/(Sici)1096-8628(19990528)84:3<245::Aid-Ajmg16>3.0.Co;2-U |
0.216 |
|
| 2007 |
Bogaerts V, Engelborghs S, Kumar-Singh S, Goossens D, Pickut B, van der Zee J, Sleegers K, Peeters K, Martin JJ, Del-Favero J, Gasser T, Dickson DW, Wszolek ZK, De Deyn PP, Theuns J, et al. A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder. Brain : a Journal of Neurology. 130: 2277-91. PMID 17681982 DOI: 10.1093/Brain/Awm167 |
0.215 |
|
| 2004 |
Ferreiro A, Ceuterick-de Groote C, Marks JJ, Goemans N, Schreiber G, Hanefeld F, Fardeau M, Martin JJ, Goebel HH, Richard P, Guicheney P, Bönnemann CG. Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene. Annals of Neurology. 55: 676-86. PMID 15122708 DOI: 10.1002/ana.20077 |
0.213 |
|
| 2010 |
Gijselinck I, Engelborghs S, Maes G, Cuijt I, Peeters K, Mattheijssens M, Joris G, Cras P, Martin JJ, De Deyn PP, Kumar-Singh S, Van Broeckhoven C, Cruts M. Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Archives of Neurology. 67: 606-16. PMID 20457961 DOI: 10.1001/Archneurol.2010.82 |
0.209 |
|
| 1987 |
Martin JJ. On some myopathies with oculomotor involvement. Acta Neurologica Belgica. 87: 207-28. PMID 3673494 |
0.208 |
|
| 1991 |
Raeymaekers P, Timmerman V, Nelis E, De Jonghe P, Hoogendijk JE, Baas F, Barker DF, Martin JJ, De Visser M, Bolhuis PA. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. Neuromuscular Disorders : Nmd. 1: 93-7. PMID 1822787 DOI: 10.1016/0960-8966(91)90055-W |
0.208 |
|
| 1997 |
Hendriks L, Thinakaran G, Harris CL, De Jonghe C, Martin JJ, Sisodia SS, Van Broeckhoven C. Processing of presenilin 1 in brains of patients with Alzheimer's disease and controls. Neuroreport. 8: 1717-21. PMID 9189920 |
0.207 |
|
| 1998 |
Tamaoka A, Fraser PE, Ishii K, Sahara N, Ozawa K, Ikeda M, Saunders AM, Komatsuzaki Y, Sherrington R, Levesque G, Yu G, Rogaeva E, Shoji S, Nee LE, Pollen DA, ... ... Martin JJ, et al. Amyloid-beta-protein isoforms in brain of subjects with PS1-linked, beta APP-linked and sporadic Alzheimer disease. Brain Research. Molecular Brain Research. 56: 178-85. PMID 9602117 DOI: 10.1016/S0169-328X(98)00044-8 |
0.206 |
|
| 2013 |
Funk F, Ceuterick-de Groote C, Martin JJ, Meinhardt A, Taratuto AL, De Bleecker J, Van Coster R, De Paepe B, Schara U, Vorgerd M, Häusler M, Koppi S, Maschke M, De Jonghe P, Van Maldergem L, et al. Morphological spectrum and clinical features of myopathies with tubular aggregates. Histology and Histopathology. 28: 1041-54. PMID 23479431 |
0.205 |
|
| 2016 |
van der Zee J, Mariën P, Crols R, Van Mossevelde S, Dillen L, Perrone F, Engelborghs S, Verhoeven J, D'aes T, Ceuterick-De Groote C, Sieben A, Versijpt J, Cras P, Martin JJ, Van Broeckhoven C. Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD. Neurology. Genetics. 2: e102. PMID 27668283 DOI: 10.1212/Nxg.0000000000000102 |
0.205 |
|
| 1987 |
Martin JJ, Bruyland M, Busch HF, Farriaux JP, Krivosic I, Ceuterick C. Pleocore disease. Multi-minicore disease and focal loss of cross striations. Acta Neuropathologica. 72: 142-9. PMID 3825514 DOI: 10.1007/BF00685976 |
0.202 |
|
| 1997 |
Beuten J, De Vriendt E, De Jonghe P, Martin JJ, Van Broeckhoven C, Timmerman V. Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24 Neuroscience Letters. 223: 69-71. PMID 9058425 DOI: 10.1016/S0304-3940(97)13400-0 |
0.202 |
|
| 2001 |
Fujigasaki H, Martin JJ, De Deyn PP, Camuzat A, Deffond D, Stevanin G, Dermaut B, Van Broeckhoven C, Dürr A, Brice A. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia. Brain : a Journal of Neurology. 124: 1939-47. PMID 11571212 DOI: 10.1093/Brain/124.10.1939 |
0.202 |
|
| 2014 |
Gallagher MD, Suh E, Grossman M, Elman L, McCluskey L, Van Swieten JC, Al-Sarraj S, Neumann M, Gelpi E, Ghetti B, Rohrer JD, Halliday G, Van Broeckhoven C, Seilhean D, Shaw PJ, ... ... Martin JJ, et al. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica. 127: 407-18. PMID 24442578 DOI: 10.1007/S00401-013-1239-X |
0.201 |
|
| 2000 |
Dermaut B, Cruts M, Backhovens H, Lübke U, Van Everbroeck B, Sciot R, Dom R, Martin JJ, Van Broeckhoven C, Cras P. Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion. Journal of Neurology. 247: 364-8. PMID 10896268 DOI: 10.1007/S004150050603 |
0.2 |
|
| 1999 |
De Jonghe P, Timmerman V, Nelis E, De Vriendt E, Löfgren A, Centerich C, Martin JJ, Van Broechhoven C. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype Archives of Neurology. 56: 1283-1288. PMID 10520946 DOI: 10.1001/Archneur.56.10.1283 |
0.2 |
|
| 1981 |
Mercelis R, Martin JJ, Martin L, Ceuterick C. Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs. Acta Neurologica Belgica. 80: 348-60. PMID 7468147 |
0.199 |
|
| 1991 |
De Bleecker J, De Reuck J, Martin JJ, Ceuterick C, Carton D, Leroy J. Autosomal recessive inheritance of polymicrogyria and dermatomyositis with paracrystalline inclusions. Clinical Neuropathology. 9: 299-304. PMID 2286022 |
0.199 |
|
| 1990 |
St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Martin JJ, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0 |
0.199 |
|
| 2001 |
Dermaut B, Kumar-Singh S, De Jonghe C, Cruts M, Löfgren A, Lübke U, Cras P, Dom R, De Deyn PP, Martin JJ, Van Broeckhoven C. Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation. Brain : a Journal of Neurology. 124: 2383-92. PMID 11701593 DOI: 10.1093/Brain/124.12.2383 |
0.198 |
|
| 2009 |
Baets J, Dierick I, Groote CC, Ende Jv, Martin JJ, Geens K, Robberecht W, Nelis E, Timmerman V, Jonghe PD. Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entity. Neuromuscular Disorders : Nmd. 19: 172-5. PMID 19167223 DOI: 10.1016/J.Nmd.2008.11.006 |
0.197 |
|
| 1992 |
Martin JJ. Adult type of neuronal ceroid lipofuscinosis. Developmental Neuroscience. 13: 331-8. PMID 1817040 DOI: 10.1159/000112182 |
0.197 |
|
| 1996 |
Ookawara T, Davé V, Willems P, Martin JJ, de Barsy T, Matthys E, Yoshida A. Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant. Archives of Biochemistry and Biophysics. 327: 35-40. PMID 8615693 DOI: 10.1006/abbi.1996.0089 |
0.197 |
|
| 1988 |
Martin JJ, Van de Vyver FL, Scholte HR, Roodhooft AM, Ceuterick C, Martin L, Luyt-Houwen IE. Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia. Journal of the Neurological Sciences. 84: 189-200. PMID 3379446 DOI: 10.1016/0022-510x(88)90124-4 |
0.197 |
|
| 2020 |
Perrone F, Bjerke M, Hens E, Sieben A, Timmers M, De Roeck A, Vandenberghe R, Sleegers K, Martin JJ, De Deyn PP, Engelborghs S, van der Zee J, Van Broeckhoven C, Cacace R. Amyloid-β cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations. Alzheimer's Research & Therapy. 12: 108. PMID 32917274 DOI: 10.1186/S13195-020-00676-5 |
0.196 |
|
| 1999 |
Pals P, Van Everbroeck B, Sciot R, Godfraind C, Robberecht W, Dom R, Laterre C, Martin JJ, Cras P. A retrospective study of Creutzfeldt-Jakob disease in Belgium. European Journal of Epidemiology. 15: 517-9. PMID 10485343 DOI: 10.1023/A:1007581313067 |
0.195 |
|
| 1989 |
Raeymaekers P, Timmerman V, De Jonghe P, Swerts L, Gheuens J, Martin JJ, Muylle L, De Winter G, Vandenberghe A, Van Broeckhoven C. Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I) American Journal of Human Genetics. 45: 953-958. PMID 2589322 |
0.194 |
|
| 2017 |
Van Mossevelde S, van der Zee J, Gijselinck I, Sleegers K, De Bleecker J, Sieben A, Vandenberghe R, Van Langenhove T, Baets J, Deryck O, Santens P, Ivanoiu A, Willems C, Bäumer V, Van den Broeck M, ... ... Martin JJ, et al. Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion. Jama Neurology. PMID 28192553 DOI: 10.1001/Jamaneurol.2016.4847 |
0.194 |
|
| 1996 |
Timmerman V, Löfgren A, Le Guern E, Liang P, De Jonghe P, Martin JJ, Verhalle D, Robberecht W, Gouider R, Brice A, Van Broeckhoven C. Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) Human Genetics. 97: 26-34. PMID 8557256 DOI: 10.1007/Bf00218828 |
0.194 |
|
| 1989 |
Destée A, Martin JJ, Muller JP, Scholte HR, Verier A, Largillière C, Warot P. [Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction]. Revue Neurologique. 145: 37-48. PMID 2646681 |
0.193 |
|
| 2006 |
Bai Y, Ianokova E, Pu Q, Ghandour K, Levinson R, Martin JJ, Ceuterick-de Groote C, Mazanec R, Seeman P, Shy ME, Li J. Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes. Archives of Neurology. 63: 1787-94. PMID 17172621 DOI: 10.1001/archneur.63.12.1787 |
0.191 |
|
| 2011 |
Guergueltcheva V, Peeters K, Baets J, Ceuterick-de Groote C, Martin JJ, Suls A, De Vriendt E, Mihaylova V, Chamova T, Almeida-Souza L, Ydens E, Tzekov C, Hadjidekov G, Gospodinova M, Storm K, et al. Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency. Neurology. 77: 2105-14. PMID 22131542 DOI: 10.1212/Wnl.0B013E31823Dc51E |
0.19 |
|
| 1996 |
Martin JJ. Hereditary disorders of the nervous system from anatomo-clinical studies to molecular biology. Acta Neurologica Belgica. 96: 240-6. PMID 8886111 |
0.189 |
|
| 1984 |
Ceuterick C, Martin JJ. Diagnostic role of skin or conjunctival biopsies in neurological disorders. An update. Journal of the Neurological Sciences. 65: 179-91. PMID 6434701 DOI: 10.1016/0022-510x(84)90082-0 |
0.189 |
|
| 2004 |
Verloes A, Bitoun P, Heuskin A, Amrom D, van de Broeck H, Nikkel SM, Chudley AE, Prasad AN, Rusu C, Covic M, Toutain A, Moraine C, Parisi MA, Patton M, Martin JJ, et al. Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndrome. American Journal of Medical Genetics. Part A. 127: 277-87. PMID 15150779 DOI: 10.1002/ajmg.a.20687 |
0.188 |
|
| 2017 |
Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, ... ... Martin JJ, et al. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases. Orphanet Journal of Rare Diseases. 12: 86. PMID 28490364 DOI: 10.1186/S13023-017-0640-2 |
0.188 |
|
| 1998 |
Ceuterick-de Groote C, Martin JJ. Extracerebral biopsy in lysosomal and peroxisomal disorders. Ultrastructural findings. Brain Pathology (Zurich, Switzerland). 8: 121-32. PMID 9458171 DOI: 10.1111/j.1750-3639.1998.tb00140.x |
0.186 |
|
| 1997 |
De Cauwer H, Heytens L, Lübke U, Ceuterick C, Martin JJ. Discordant light microscopic, electron microscopic, and in vitro contracture study findings in a family with central core disease. Clinical Neuropathology. 16: 237-42. PMID 9323448 |
0.185 |
|
| 1967 |
Myle G, Radermecker J, Martin JJ. [On nemaline myopathy]. Psychiatria Et Neurologia. 154: 37-49. PMID 6051911 |
0.185 |
|
| 2003 |
Nijssen PC, Ceuterick C, van Diggelen OP, Elleder M, Martin JJ, Teepen JL, Tyynelä J, Roos RA. Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency. Brain Pathology (Zurich, Switzerland). 13: 574-81. PMID 14655761 |
0.185 |
|
| 2006 |
Pirici D, Vandenberghe R, Rademakers R, Dermaut B, Cruts M, Vennekens K, Cuijt I, Lübke U, Ceuterick C, Martin JJ, Van Broeckhoven C, Kumar-Singh S. Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family. Journal of Neuropathology and Experimental Neurology. 65: 289-301. PMID 16651890 DOI: 10.1097/01.Jnen.0000205147.39210.C7 |
0.185 |
|
| 2012 |
Martin JJ. Spinocerebellar ataxia type 7. Handbook of Clinical Neurology. 103: 475-91. PMID 21827908 DOI: 10.1016/B978-0-444-51892-7.00030-9 |
0.185 |
|
| 1997 |
Berwaerts J, Verhelst J, Vandenbroucke M, Abs R, Martin JJ, Mahler C. Thyrotoxic periodic paralysis, an unusual cause of hypokalemic periodic paralysis. Acta Neurologica Belgica. 96: 301-6. PMID 9008779 |
0.184 |
|
| 1997 |
Timmerman V, Rautenstrauss B, Reiter LT, Koeuth T, Löfgren A, Liehr T, Nelis E, Bathke KD, De Jonghe P, Grehl H, Martin JJ, Lupski JR, Van Broeckhoven C. Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent Journal of Medical Genetics. 34: 43-49. PMID 9032649 DOI: 10.1136/Jmg.34.1.43 |
0.183 |
|
| 1977 |
Neimann N, Martin JJ, Vidailhet M, Floquet J, Pierson M, Bajolle A. [Multiple systemic atrophies, mental retardation, neurogenic amyotrophy and congenital bone fragility. A new neuro-generative disorder]. Journal of the Neurological Sciences. 30: 287-97. PMID 187737 DOI: 10.1016/0022-510X(76)90134-9 |
0.183 |
|
| 1999 |
Deprez M, D'Hooghe M, Misson JP, de Leval L, Ceuterick C, Reznik M, Martin JJ. Infantile and juvenile presentations of Alexander's disease: a report of two cases. Acta Neurologica Scandinavica. 99: 158-65. PMID 10100959 DOI: 10.1111/j.1600-0404.1999.tb07338.x |
0.18 |
|
| 1994 |
Cruts M, Backhovens H, Martin JJ, van Broeckhoven C. Genetic analysis of the cellular oncogene fos in patients with chromosome 14 encoded Alzheimer's disease. Neuroscience Letters. 174: 97-100. PMID 7970166 DOI: 10.1016/0304-3940(94)90128-7 |
0.179 |
|
| 1993 |
Ceuterick C, Martin JJ. Electron microscopic features of skin in neurometabolic disorders. Journal of the Neurological Sciences. 112: 15-29. PMID 1469426 DOI: 10.1016/0022-510x(92)90126-6 |
0.179 |
|
| 1998 |
Houlden H, Crook R, Backhovens H, Prihar G, Baker M, Hutton M, Rossor M, Martin JJ, Van Broeckhoven C, Hardy J. ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families. American Journal of Medical Genetics. 81: 117-21. PMID 9514597 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<117::Aid-Ajmg19>3.0.Co;2-M |
0.178 |
|
| 1985 |
Martin JJ, Ceuterick C, Mercelis R, Amrom D. Familial periodic paralysis with hypokalaemia. Study of a muscle biopsy in the myopathic stage of the disorder. Acta Neurologica Belgica. 84: 233-42. PMID 6524295 |
0.177 |
|
| 1980 |
Martin JJ. [A new observation of cherry-red spot myoclonus syndrome (author's transl)]. Acta Neurologica Belgica. 80: 30-6. PMID 7361541 |
0.175 |
|
| 1996 |
Hendriks L, Jonghe CDXs, Cras P, Martin JJ, Broeckhoven CV. Beta-amyloid precursor protein and early-onset Alzheimer's disease. Ciba Foundation Symposium. 199: 170-80. PMID 8915610 |
0.174 |
|
| 1984 |
Martin JJ, Ceuterick CM, Leroy JG, Devos EA, Roelens JG. The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case. Neuropediatrics. 15: 43-8. PMID 6200796 DOI: 10.1055/s-2008-1052339 |
0.174 |
|
| 1989 |
Roodhooft AM, Van Acker KJ, Van Thienen MN, Martin JJ, Ceuterick C. Marshall-Smith syndrome: new aspects. Neuropediatrics. 19: 179-82. PMID 3205374 DOI: 10.1055/s-2008-1052441 |
0.174 |
|
| 1981 |
Loonen MC, Busch HF, Koster JF, Martin JJ, Niermeijer MF, Schram AW, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM. A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies. Neurology. 31: 1209-16. PMID 6810200 DOI: 10.1212/WNL.31.10.1209 |
0.173 |
|
| 1988 |
Martin JJ, Ceuterick C. The contribution of pathology to the study of storage disorders. Pathology, Research and Practice. 183: 375-85. PMID 2847122 DOI: 10.1016/S0344-0338(88)80083-9 |
0.173 |
|
| 1992 |
Abs R, Van Vyve M, Willems PJ, Neetens I, Van der Auwera B, Van den Ende E, Van de Kelft E, Beckers A, Van Marck E, Martin JJ. The association of astrocytoma and pituitary adenoma in a patient with alcaptonuria. Journal of the Neurological Sciences. 108: 32-4. PMID 1624949 DOI: 10.1016/0022-510x(92)90184-m |
0.172 |
|
| 2002 |
Ozsarlak O, Schepens E, Parizel PM, Van Goethem JW, Vanhoenacker F, De Schepper AM, Martin JJ. Hereditary neuromuscular diseases. European Journal of Radiology. 40: 184-97. PMID 11731207 DOI: 10.1016/S0720-048X(01)00399-0 |
0.171 |
|
| 2012 |
Verhagen MM, Martin JJ, van Deuren M, Ceuterick-de Groote C, Weemaes CM, Kremer BH, Taylor MA, Willemsen MA, Lammens M. Neuropathology in classical and variant ataxia-telangiectasia. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 32: 234-44. PMID 22017321 DOI: 10.1111/j.1440-1789.2011.01263.x |
0.17 |
|
| 1992 |
Heytens L, Martin JJ, Van de Kelft E, Bossaert LL. In vitro contracture tests in patients with various neuromuscular diseases. British Journal of Anaesthesia. 68: 72-5. PMID 1739572 DOI: 10.1093/bja/68.1.72 |
0.169 |
|
| 2001 |
Van Everbroeck B, Pals P, Quoilin S, Martin JJ, Cras P. The many faces of human prion diseases in Belgium and the world. Acta Neurologica Belgica. 101: 81-7. PMID 11486562 |
0.169 |
|
| 2000 |
Van Maldergem L, Tuerlinckx D, Wanders RJ, Vianey-Saban C, Van Hoof F, Martin JJ, Fourneau C, Gillerot Y, Bachy A. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings. European Journal of Pediatrics. 159: 108-12. PMID 10653342 DOI: 10.1007/s004310050022 |
0.169 |
|
| 1994 |
Broeckhoven CV, Backhovens H, Cruts M, Martin JJ, Crook R, Houlden H, Hardy J. APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease Neuroscience Letters. 169: 179-180. PMID 8047278 DOI: 10.1016/0304-3940(94)90385-9 |
0.168 |
|
| 1993 |
Willems PJ, Van Roy BC, Kleijer WJ, Van der Kraan M, Martin JJ. Atypical clinical presentation of ataxia telangiectasia. American Journal of Medical Genetics. 45: 777-82. PMID 8456862 DOI: 10.1002/ajmg.1320450624 |
0.168 |
|
| 1995 |
De Wilde F, D'Haens M, Smet H, Martin JJ, Tassignon MJ. Surgical treatment of myogenic blepharoptosis Bulletin De La SociéTé Belge D'Ophtalmologie. 255: 139-146. PMID 7496569 |
0.168 |
|
| 1985 |
Cartigny B, Libert J, Fensom AH, Martin JJ, Dhondt JL, Wyart D, Fontaine G, Farriaux JP. Clinical diagnosis of a new case of ceramidase deficiency (Farber's disease). Journal of Inherited Metabolic Disease. 8: 8. PMID 3921761 DOI: 10.1007/BF01805474 |
0.168 |
|
| 1982 |
Martin JJ, Lowenthal A, Ceuterick C, Gacoms H. Adrenomyeloneuropathy. A report on two families. Journal of Neurology. 226: 221-32. PMID 6174703 DOI: 10.1007/BF00313395 |
0.168 |
|
| 1993 |
Villanova M, De Clerck LS, Cras P, Ceuterick C, Van Marck E, Guazzi GC, Martin JJ. Eosinophilia-myalgia syndrome: a clinicopathological study of four patients. Clinical Neuropathology. 12: 201-3. PMID 8403629 |
0.167 |
|
| 2019 |
Cacace R, Heeman B, Van Mossevelde S, De Roeck A, Hoogmartens J, De Rijk P, Gossye H, De Vos K, De Coster W, Strazisar M, De Baets G, Schymkowitz J, Rousseau F, Geerts N, De Pooter T, ... ... Martin JJ, et al. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability. Acta Neuropathologica. PMID 30874922 DOI: 10.1007/S00401-019-01976-3 |
0.165 |
|
| 1981 |
Mercelis R, Martin JJ, Dehaene I, de Barsy T, Van den Berghe G. Myoadenylate deaminase deficiency in a patient with facial and limb girdle myopathy. Journal of Neurology. 225: 157-66. PMID 6167680 DOI: 10.1007/BF00313744 |
0.165 |
|
| 2002 |
Nijssen PC, Brusse E, Leyten AC, Martin JJ, Teepen JL, Roos RA. Autosomal dominant adult neuronal ceroid lipofuscinosis: parkinsonism due to both striatal and nigral dysfunction. Movement Disorders : Official Journal of the Movement Disorder Society. 17: 482-7. PMID 12112194 DOI: 10.1002/mds.10104 |
0.164 |
|
| 2004 |
Van Everbroeck B, Dobbeleir I, De Waele M, De Deyn P, Martin JJ, Cras P. Differential diagnosis of 201 possible Creutzfeldt-Jakob disease patients. Journal of Neurology. 251: 298-304. PMID 15015009 DOI: 10.1007/s00415-004-0311-9 |
0.164 |
|
| 2000 |
Meca-Lallana JE, Martín JJ, Lucas C, Marín J, Gomariz J, Valenti JA, de Lara A, Fernández-Barreiro A. [Susac syndrome: clinical and diagnostic approach. A new case report]. Revista De Neurologia. 29: 1027-32. PMID 10637864 |
0.164 |
|
| 1993 |
Martin JJ, Ceuterick C, Lübke U, Van Broeckhoven C. Duchenne muscular dystrophy immunohistochemistry of foetal muscles. Acta Neurologica Belgica. 93: 130-8. PMID 7688489 |
0.162 |
|
| 1990 |
Rodesch G, Van Bogaert P, Mavroudakis N, Parizel PM, Martin JJ, Segebarth C, Van Vyve M, Baleriaux D, Hildebrand J. Neuroradiologic findings in leptomeningeal carcinomatosis: the value interest of gadolinium-enhanced MRI. Neuroradiology. 32: 26-32. PMID 2333130 DOI: 10.1007/Bf00593937 |
0.16 |
|
| 1992 |
Martin JJ, Guazzi GC. Schilder's diffuse sclerosis. Developmental Neuroscience. 13: 267-73. PMID 1817032 DOI: 10.1159/000112172 |
0.159 |
|
| 1976 |
Dehaene I, Martin JJ. "Locked-in" syndrome. A clinico-pathological study of two cases. European Neurology. 14: 81-9. PMID 1248496 DOI: 10.1159/000114730 |
0.159 |
|
| 1997 |
De Jonghe P, Timmerman V, FitzPatrick D, Spoelders P, Martin JJ, Van Broeckhoven C. Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family Journal of Neurology Neurosurgery and Psychiatry. 62: 570-573. PMID 9219740 DOI: 10.1136/Jnnp.62.6.570 |
0.159 |
|
| 1983 |
Dubois B, Martin JJ, Develter S, Guérin M, Loeuille GA, Debeugny P, Farriaux JP. [Centronuclear myopathy. Apropos of a new case]. La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris. 59: 561-5. PMID 6302904 |
0.159 |
|
| 1989 |
Raeymaekers P, De Jonghe P, Backhovens H, Wehnert A, De Winter G, Swerts L, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers. Neurology. 39: 844-6. PMID 2725880 DOI: 10.1212/wnl.39.6.844 |
0.158 |
|
| 1989 |
Raeymaekers P, De Jonghe P, Swerts L, De Winter G, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Exclusion analysis of Charcot-Marie-Tooth neuropathy (CMT1) with chromosome 1p markers. Cytogenetics and Cell Genetics. 50: 178-80. PMID 2570676 DOI: 10.1159/000132756 |
0.158 |
|
| 1991 |
Martin JJ, Gheuens J, Bruyland M, Cras P, Vandenberghe A, Masters CL, Beyreuther K, Dom R, Ceuterick C, Lübke U. Early-onset Alzheimer's disease in 2 large Belgian families. Neurology. 41: 62-8. PMID 1985297 DOI: 10.1212/Wnl.41.1.62 |
0.158 |
|
| 1997 |
Ceuterick C, Martin JJ. Sporadic early adult-onset distal myopathy with rimmed vacuoles: immunohistochemistry and electron microscopy. Journal of the Neurological Sciences. 139: 190-6. PMID 8856652 |
0.157 |
|
| 1979 |
Liessens JL, Monstrey J, Vanden Eeckhout E, Djudzman R, Martin JJ. Bismuth encephalopathy. A clinical and anatomo-pathological report of one case. Acta Neurologica Belgica. 78: 301-9. PMID 716834 |
0.155 |
|
| 2013 |
van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, ... ... Martin JJ, et al. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. Human Mutation. 34: 363-73. PMID 23111906 DOI: 10.1002/Humu.22244 |
0.154 |
|
| 1986 |
Lenders MB, Martin JJ, de Barsy T, Ceuterick C, Marchau M. Acid maltase deficiency in adults. A study of five cases. Acta Neurologica Belgica. 86: 152-60. PMID 3090848 |
0.154 |
|
| 1998 |
Courtens W, Tjalma W, Messiaen L, Vamos E, Martin JJ, Van Bogaert E, Keersmaekers G, Meulyzer P, Wauters J. Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly. American Journal of Medical Genetics. 77: 188-97. PMID 9605585 |
0.154 |
|
| 1986 |
Martin JJ, Vercruyssen A, de Barsy T, Ceuterick C. Muscle carnitine deficiency in old age. Case report and therapeutic results. Clinical Neurology and Neurosurgery. 87: 275-81. PMID 4092408 DOI: 10.1016/0303-8467(85)90135-0 |
0.153 |
|
| 1998 |
Decaestecker C, Camby I, Gordower L, Dewitte O, Cras P, Martin JJ, Pasteels JL, Van Ham P, Brotchi J, Kiss R, Salmon I. Characterization of astroglial versus oligodendroglial phenotypes in glioblastomas by means of quantitative morphonuclear variables generated by computer-assisted microscopy. Journal of Neuropathology and Experimental Neurology. 57: 791-802. PMID 9720494 DOI: 10.1097/00005072-199808000-00008 |
0.153 |
|
| 2000 |
Van Everbroeck B, Pals P, Dziedzic T, Dom R, Godfraind C, Sciot R, Brucher JM, Martin JJ, Cras P. Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings. Acta Neuropathologica. 99: 358-64. PMID 10787033 DOI: 10.1007/S004010051136 |
0.153 |
|
| 1986 |
Walter GF, Brucher JM, Martin JJ, Ceuterick C, Pilz P, Freund M. Leigh's disease--several nosological entities with an identical histopathological complex? Neuropathology and Applied Neurobiology. 12: 95-107. PMID 3703157 DOI: 10.1111/j.1365-2990.1986.tb00683.x |
0.153 |
|
| 2000 |
Palmeri S, Villanova M, Malandrini A, van Diggelen OP, Huijmans JG, Ceuterick C, Rufa A, DeFalco D, Ciacci G, Martin JJ, Guazzi G. Type I sialidosis: a clinical, biochemical and neuroradiological study. European Neurology. 43: 88-94. PMID 10686466 |
0.153 |
|
| 2002 |
Van Maldergem L, Trijbels F, DiMauro S, Sindelar PJ, Musumeci O, Janssen A, Delberghe X, Martin JJ, Gillerot Y. Coenzyme Q-responsive Leigh's encephalopathy in two sisters. Annals of Neurology. 52: 750-4. PMID 12447928 DOI: 10.1002/ana.10371 |
0.153 |
|
| 1990 |
Timmerman V, Raeymaekers P, De Jonghe P, De Winter G, Swerts L, Jacobs K, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Assignment of the charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12 American Journal of Human Genetics. 47: 680-685. PMID 2220808 |
0.153 |
|
| 1998 |
Dehaene I, Cras P, Parizel PM, Martin JJ. Clinical-pathological conference. Acta Neurologica Belgica. 98: 41-8. PMID 9606440 |
0.152 |
|
| 1992 |
Blom HJ, Davidson AJ, Finkelstein JD, Luder AS, Bernardini I, Martin JJ, Tangerman A, Trijbels JM, Mudd SH, Goodman SI. Persistent hypermethioninaemia with dominant inheritance. Journal of Inherited Metabolic Disease. 15: 188-97. PMID 1527987 DOI: 10.1007/Bf01799629 |
0.152 |
|
| 2000 |
De Praeter CM, Gerwig GJ, Bause E, Nuytinck LK, Vliegenthart JF, Breuer W, Kamerling JP, Espeel MF, Martin JJ, De Paepe AM, Chan NW, Dacremont GA, Van Coster RN. A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency. American Journal of Human Genetics. 66: 1744-56. PMID 10788335 |
0.152 |
|
| 2003 |
Ingelbrecht SN, Wynants H, Moorkens G, Gielen JL, Martin JJ, Stevens W, De Clerck LS. An unusual case of generalized oedema. Acta Clinica Belgica. 58: 201-4. PMID 12945481 DOI: 10.1179/acb.2003.58.3.009 |
0.152 |
|
| 1984 |
Dehaene I, Dom R, Martin JJ. [The locked-in syndrome. Clinical study of 10 cases]. Acta Neurologica Belgica. 84: 12-20. PMID 6720245 |
0.152 |
|
| 2008 |
Ceulemans BP, Storm K, Reyniers E, Callewaert L, Martin JJ. Muscle pain as the only presenting symptom in a girl with dystrophinopathy. Pediatric Neurology. 38: 64-6. PMID 18054699 DOI: 10.1016/j.pediatrneurol.2007.09.006 |
0.151 |
|
| 1987 |
Mercelis R, Martin JJ, de Barsy T, Van den Berghe G. Myoadenylate deaminase deficiency: absence of correlation with exercise intolerance in 452 muscle biopsies. Journal of Neurology. 234: 385-9. PMID 3655841 DOI: 10.1007/BF00314082 |
0.151 |
|
| 1992 |
Martin JJ, Leroy J, Ceuterick C, Lübke U, Van Buggenhout E, Van Vuchelen J, Van Broeckhoven C. Becker-type muscular dystrophy. Report of a family with one postmortem study. Clinical Neurology and Neurosurgery. S123-6. PMID 1320486 DOI: 10.1016/0303-8467(92)90045-5 |
0.15 |
|
| 1972 |
Martin JJ, Philippart M, Van Hauwaert J, Callahan JW, Deberdt R. Niemann-Pick disease (Crocker's group A). Late onset and pigmentary degeneration resembling Hallervorden-Spatz syndrome. Archives of Neurology. 27: 45-51. PMID 5049680 DOI: 10.1001/archneur.1972.00490130047007 |
0.149 |
|
| 1984 |
Martin JJ, Leroy JG, van Eygen M, Ceuterick C. I-cell disease. A further report on its pathology. Acta Neuropathologica. 64: 234-42. PMID 6093421 DOI: 10.1007/BF00688114 |
0.148 |
|
| 1998 |
Ceuterick C, Lübke U, Cras P, Martin JJ. Astroglial tangles in the hippocampus of two patients with Down syndrome and Alzheimer neuropathology. Ultrastructural Pathology. 22: 161-3. PMID 9615386 DOI: 10.3109/01913129809032272 |
0.148 |
|
| 2021 |
Sieben A, Van Langenhove T, Vermeiren Y, Gossye H, Praet M, Vanhauwaert D, Cousaert C, Engelborghs S, Raedt R, Boon P, Santens P, De Deyn PP, Bracke KR, De Meulemeester K, Van Broeckhoven C, ... Martin JJ, et al. Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration. Journal of Neuropathology and Experimental Neurology. PMID 33638350 DOI: 10.1093/jnen/nlab010 |
0.148 |
|
| 2003 |
Van Everbroeck B, Quoilin S, Boons J, Martin JJ, Cras P. A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 1210-4. PMID 12933920 DOI: 10.1136/jnnp.74.9.1210 |
0.148 |
|
| 2017 |
Grond-Ginsbach C, Brandt T, Kloss M, Aksay SS, Lyrer P, Traenka C, Erhart P, Martin JJ, Altintas A, Siva A, de Freitas GR, Thie A, Machetanz J, Baumgartner RW, Dichgans M, et al. Next generation sequencing analysis of patients with familial cervical artery dissection. European Stroke Journal. 2: 137-143. PMID 31008308 DOI: 10.1177/2396987317693402 |
0.147 |
|
| 1997 |
O'Rawe A, Mitchison HM, Williams R, Wheeler R, Andermann E, Andermann F, Hart YM, Martin JJ, Philippart M, Stephenson JB, Gardiner RM, Mole SE. Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits. Neuropediatrics. 28: 21-2. PMID 9151314 DOI: 10.1055/S-2007-973659 |
0.147 |
|
| 2000 |
Deprez M, de Groote CC, Gollogly L, Reznik M, Martin JJ. Clinical and neuropathological parameters affecting the diagnostic yield of nerve biopsy. Neuromuscular Disorders : Nmd. 10: 92-8. PMID 10714582 DOI: 10.1016/s0960-8966(99)00094-2 |
0.146 |
|
| 1978 |
Kluyskens Y, Bossaert L, Snoeck J, Martin JJ. Idiopathic orthostatic hypotension and the Shy and Drager syndrome; Physiological studies in four cases; pathological report of one case. Acta Cardiologica. 32: 317-35. PMID 304652 |
0.145 |
|
| 1998 |
Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion. Human Molecular Genetics. 7: 177-86. PMID 9425224 DOI: 10.1093/Hmg/7.2.177 |
0.145 |
|
| 2020 |
Martin S, Smolders S, Van den Haute C, Heeman B, van Veen S, Crosiers D, Beletchi I, Verstraeten A, Gossye H, Gelders G, Pals P, Hamouda NN, Engelborghs S, Martin JJ, Eggermont J, et al. Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export. Acta Neuropathologica. PMID 32172343 DOI: 10.1007/S00401-020-02145-7 |
0.145 |
|
| 1977 |
Martin JJ, De Barsy T, Leroy JG, Palladini G. Acid maltase deficiency (type II glycogenosis). Morphological and biochemical study of a childhood phenotype. Journal of the Neurological Sciences. 30: 155-66. PMID 1068222 DOI: 10.1016/0022-510x(76)90263-x |
0.145 |
|
| 1997 |
Callebaut DP, Cras P, Martin JJ. Prolonged and atypical course in some cases of subacute sclerosing panencephalitis. Acta Neurologica Belgica. 97: 39-44. PMID 9107344 |
0.145 |
|
| 1980 |
Martin JJ, Dompas B, Ceuterick C, Jacobs K. Adrenomyeloneuropathy and adrenoleukodystrophy in two brothers. European Neurology. 19: 281-7. PMID 6249605 DOI: 10.1159/000115163 |
0.145 |
|
| 1978 |
Martin JJ, Ceuterick C, Joris C, Martens C. [Centronuclear myopathy (author's transl)]. Acta Neurologica Belgica. 77: 285-99. PMID 145158 |
0.144 |
|
| 1977 |
Martin JJ, Martin L, Ceuterick C. Encephalopathy associated with lamellar residual bodies in astrocytes (Towfighi, Grover and Gonatas 1975):a new observation. Neuropadiatrie. 8: 181-9. PMID 195236 DOI: 10.1055/s-0028-1091515 |
0.144 |
|
| 1991 |
van Duijn CM, van Broeckhoven C, Hardy JA, Goate AM, Rossor MN, Vandenberghe A, Martin JJ, Hofman A, Mullan MJ. Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease. The British Journal of Psychiatry : the Journal of Mental Science. 158: 471-4. PMID 2054561 DOI: 10.1192/Bjp.158.4.471 |
0.144 |
|
| 1978 |
Libert J, Martin JJ, Evrard P, Verougstraete C, Danis P. [The ceroid-lipofuscinoses: ocular ultrastructure and diagnosis by conjunctival biopsy (author's transl)]. Archives D'Ophtalmologie. 37: 613-28. PMID 146472 |
0.143 |
|
| 1998 |
MARTIN JJ. [Subdural hematoma with late manifestations. Apropos of 6 clinical cases]. Acta Neurologica Et Psychiatrica Belgica. 61: 1024-59. PMID 14470398 |
0.143 |
|
| 1967 |
Terzian H, Rizzuto N, Patarnello L, Martin JJ. [On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation]. Acta Neuropathologica. Suppl 3:37-41. PMID 6074647 |
0.142 |
|
| 2001 |
Van Everbroeck B, Croes EA, Pals P, Dermaut B, Jansen G, van Duijn CM, Cruts M, Van Broeckhoven C, Martin JJ, Cras P. Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype. Neuroscience Letters. 313: 69-72. PMID 11684342 DOI: 10.1016/S0304-3940(01)02264-9 |
0.142 |
|
| 1981 |
Mercelis R, Demeester J, Martin JJ. Neurogenic scapuloperoneal syndrome in childhood. Journal of Neurology, Neurosurgery, and Psychiatry. 43: 888-96. PMID 7441268 DOI: 10.1136/jnnp.43.10.888 |
0.142 |
|
| 1986 |
Martin JJ, Leroy JG. Thalamic lesions in a patient with Menkes kinky-hair disease. Clinical Neuropathology. 4: 206-9. PMID 4064386 |
0.141 |
|
| 1992 |
Truyen L, Gheuens J, Parizel PM, Van de Vyver FL, Martin JJ. Long term follow-up of multiple sclerosis by standardized, non-contrast-enhanced magnetic resonance imaging. Journal of the Neurological Sciences. 106: 35-40. PMID 1779237 DOI: 10.1016/0022-510x(91)90191-9 |
0.14 |
|
| 1983 |
Caimi L, Tettamanti G, Berra B, Omodeo Sale F, Borrone C, Gatti R, Durand P, Martin JJ. Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency. Journal of Inherited Metabolic Disease. 5: 218-24. PMID 6820444 DOI: 10.1007/BF02179146 |
0.14 |
|
| 1997 |
Martin JJ, Ceuterick C, Van Goethem G. On a dominantly inherited myopathy with tubular aggregates. Neuromuscular Disorders : Nmd. 7: 512-20. PMID 9447609 |
0.139 |
|
| 1989 |
Raeymaekers P, De Jonghe P, Swerts L, Muylle L, Gheuens J, Martin JJ, Van Broeckhoven C, Vandenberghe A. Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy. Journal of the Neurological Sciences. 88: 145-50. PMID 3225617 DOI: 10.1016/0022-510x(88)90212-2 |
0.139 |
|
| 1980 |
De Jonghe P, Martin JJ, Budka H, Ceuterick C. Cerebral manifestations of Whipple's disease. Acta Neurologica Belgica. 79: 305-13. PMID 95079 |
0.137 |
|
| 1967 |
van Bogaert L, Kissel P, Schmitt J, Martin JJ, Claes C, Duc M, Royer R, Barrucand D, Grignon J, Floquet J. [Myopathic syndrome in the course of Gamstorp's disease. Anatomical study]. Acta Neurologica Et Psychiatrica Belgica. 67: 133-42. PMID 4227039 |
0.137 |
|
| 1978 |
Martin JJ, Ceuterick C. Morphological study of skin biopsy specimens: a contribution to the diagnosis of metabolic disorders with involvement of the nervous system. Journal of Neurology, Neurosurgery, and Psychiatry. 41: 232-48. PMID 416179 DOI: 10.1136/jnnp.41.3.232 |
0.136 |
|
| 2018 |
Dekker AD, Vermeiren Y, Carmona-Iragui M, Benejam B, Videla L, Gelpi E, Aerts T, Van Dam D, Fernández S, Lleó A, Videla S, Sieben A, Martin JJ, Blesa R, et al. Monoaminergic impairment in Down syndrome with Alzheimer's disease compared to early-onset Alzheimer's disease. Alzheimer's & Dementia (Amsterdam, Netherlands). 10: 99-111. PMID 29780859 DOI: 10.1016/j.dadm.2017.11.001 |
0.136 |
|
| 2002 |
Kumar-Singh S, Cras P, Wang R, Kros JM, van Swieten J, Lübke U, Ceuterick C, Serneels S, Vennekens K, Timmermans JP, Van Marck E, Martin JJ, van Duijn CM, Van Broeckhoven C. Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric. The American Journal of Pathology. 161: 507-20. PMID 12163376 DOI: 10.1016/S0002-9440(10)64207-1 |
0.135 |
|
| 1997 |
Martin JJ. Neuropathology of peroxisomal diseases. Journal of Inherited Metabolic Disease. 19-33. PMID 9053552 DOI: 10.1007/BF00711426 |
0.135 |
|
| 1997 |
Krols L, Martin JJ, David G, Van Regemorter N, Benomar A, Löfgren A, Stevanin G, Dürr A, Brice A, Van Broeckhoven C. Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1. Human Genetics. 99: 225-32. PMID 9048926 DOI: 10.1007/s004390050344 |
0.135 |
|
| 1993 |
Willems PJ, Colpaert C, Vaerenbergh M, Van Thienen MN, Parizel PM, Van Marck E, Schuerwegh WH, Martin JJ. Multiple pterygium syndrome with body asymmetry. American Journal of Medical Genetics. 47: 106-11. PMID 8368239 DOI: 10.1002/ajmg.1320470122 |
0.135 |
|
| 1992 |
Heytens LG, Even B, Martin JJ, Bossaert LL. Differential diagnosis of anesthesia induced rhabdomyolysis. A case report. Acta Neurologica Belgica. 91: 303-7. PMID 1781267 |
0.134 |
|
| 1973 |
Martin JJ. [Clinical and pathological description of Gayet-Wernicke encephalopathy and the adult form of Leigh's encephalopathy]. Acta Neurologica Belgica. 72: 347-54. PMID 4653790 |
0.134 |
|
| 1995 |
Dams E, Van de Kelft EJ, Martin JJ, Verlooy J, Willems PJ. Instability of microsatellites in human gliomas. Cancer Research. 55: 1547-9. PMID 7882363 |
0.134 |
|
| 1977 |
Libert J, Martin JJ, Ceuterick C, Danis P. Ocular ultrastructural study in a fetus with type II glycogenosis. The British Journal of Ophthalmology. 61: 476-82. PMID 268211 DOI: 10.1136/bjo.61.7.476 |
0.134 |
|
| 1997 |
De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C. Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees. European Journal of Human Genetics : Ejhg. 4: 260-6. PMID 8946171 DOI: 10.1159/000472212 |
0.134 |
|
| 1973 |
Martin JJ, de Barsy T, van Hoof F, Palladini G. Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle. Acta Neuropathologica. 23: 229-44. PMID 4511788 DOI: 10.1007/BF00687878 |
0.134 |
|
| 1977 |
Martin JJ, Clara R, Ceuterick C, Joris C. Is congenital fibre type disproportion a true myopathy? Acta Neurologica Belgica. 76: 335-44. PMID 1070214 |
0.133 |
|
| 2005 |
De Deyn PP, Engelborghs S, Saerens J, Goeman J, Mariën P, Maertens K, Nagels G, Martin JJ, Pickut BA. The Middelheim Frontality Score: a behavioural assessment scale that discriminates frontotemporal dementia from Alzheimer's disease. International Journal of Geriatric Psychiatry. 20: 70-9. PMID 15578673 DOI: 10.1002/Gps.1249 |
0.133 |
|
| 1981 |
Loonen MC, Schram AW, Koster JF, Niermeijer MF, Busch HF, Martin JJ, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM. Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency). Clinical Genetics. 19: 55-63. PMID 7006871 DOI: 10.1111/j.1399-0004.1981.tb00668.x |
0.133 |
|
| 1992 |
Raeymaekers P, Timmerman V, Nelis E, Hul WV, Jonghe PD, Martin JJ, Broeckhoven CV. Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. Journal of Medical Genetics. 29: 5-11. PMID 1552545 DOI: 10.1136/Jmg.29.1.5 |
0.133 |
|
| 1979 |
Dom R, Brucher JM, Ceuterick C, Carton H, Martin JJ. Adult ceroid-lipofuscinosis (Kufs' disease) in two brothers. Retinal and visceral storage in one; diagnostic muscle biopsy in the other. Acta Neuropathologica. 45: 67-72. PMID 760366 DOI: 10.1007/BF00691807 |
0.133 |
|
| 1993 |
Ceuterick C, Martin JJ, Martens C. Hyaline bodies in skeletal muscle of a patient with a mild chronic nonprogressive congenital myopathy. Clinical Neuropathology. 12: 79-83. PMID 7682901 |
0.132 |
|
| 1985 |
Bruyland M, Liebaers I, Sacre L, Vandeplas Y, De Meirleir L, Martin JJ. Neonatal myotubular myopathy with a probable X-linked inheritance: observations on a new family with a review of the literature. Journal of Neurology. 231: 220-2. PMID 6512577 DOI: 10.1007/BF00313942 |
0.132 |
|
| 1990 |
Hassoun A, Verstraeten L, Mercelis R, Martin JJ. Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old man. Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie. 27: 781-6. PMID 2600550 DOI: 10.1515/cclm.1989.27.10.781 |
0.131 |
|
| 1976 |
Martin JJ, de Barsy T, den Tandt WR. Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study. Journal of Neurology. 213: 105-18. PMID 60470 DOI: 10.1007/BF00313272 |
0.13 |
|
| 2009 |
Flannery T, Kano H, Martin JJ, Niranjan A, Flickinger JC, Lunsford LD, Kondziolka D. Boost radiosurgery as a strategy after failure of initial management of pediatric primitive neuroectodermal tumors: Clinical article Journal of Neurosurgery: Pediatrics. 3: 205-210. PMID 19338466 DOI: 10.3171/2008.11.Peds08268 |
0.13 |
|
| 1973 |
Radermecker J, Martin JJ. [Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects]. Bulletin De L'Academie Royale De Medecine De Belgique. 12: 459-502. PMID 4662801 |
0.13 |
|
| 2006 |
Willekens BM, Rooker S, Dua G, Appel B, Martin JJ, Crols R, De Deyn PP. Central nervous system metastases of pulmonary adenocarcinoma mimicking neurofibromatosis type 2. Acta Neurologica Belgica. 106: 87-9. PMID 16898259 |
0.13 |
|
| 1983 |
Vercruyssen A, Martin JJ, Mercelis R. Neurophysiological studies in adrenomyeloneuropathy. A report on five cases. Journal of the Neurological Sciences. 56: 327-36. PMID 6294257 DOI: 10.1016/0022-510x(82)90153-8 |
0.129 |
|
| 1984 |
Vrints C, Mercelis R, Vanagt E, Snoeck J, Martin JJ. Cardiac manifestations of Becker-type muscular dystrophy. Acta Cardiologica. 38: 479-86. PMID 6606925 |
0.129 |
|
| 2017 |
Grond-Ginsbach C, Chen B, Krawczak M, Pjontek R, Ginsbach P, Jiang Y, Abboud S, Arnold ML, Bersano A, Brandt T, Caso V, Debette S, Dichgans M, Geschwendtner A, Giacalone G, ... Martin JJ, et al. Genetic Imbalance in Patients with Cervical Artery Dissection. Current Genomics. 18: 206-213. PMID 28367076 DOI: 10.2174/1389202917666160805152627 |
0.129 |
|
| 1988 |
Martin JJ, Libert J, Ceuterick C. Ultrastructure of brain and retina in Kufs' disease (adult type-ceroid-lipofuscinosis). Clinical Neuropathology. 6: 231-5. PMID 2827925 |
0.128 |
|
| 1977 |
Martin JJ, Ceuterick C, Leroy JG. [Skin biopsy in the diagnosis of metabolic encephalopathies]. Revue Neurologique. 132: 639-51. PMID 825940 |
0.128 |
|
| 1996 |
Timmerman V, De Jonghe P, Simokovic S, Löfgren A, Beuten J, Nelis E, Ceuterick C, Martin JJ, Van Broeckhoven C. Distal hereditary motor neuropathy type II (distal HMN II): Mapping of a locus to chromosome 12q24 Human Molecular Genetics. 5: 1065-1069. PMID 8817349 DOI: 10.1093/Hmg/5.7.1065 |
0.128 |
|
| 1987 |
Ebinger G, Bruyland M, Martin JJ, Herregodts P, Cras P, Michotte Y, Gommé L. Distribution of biogenic amines and their catabolites in brains from patients with Alzheimer's disease. Journal of the Neurological Sciences. 77: 267-83. PMID 3819769 DOI: 10.1016/0022-510X(87)90128-6 |
0.127 |
|
| 2006 |
Martin JJ, Hausser I, Lyrer P, Busse O, Schwarz R, Schneider R, Brandt T, Kloss M, Schwaninger M, Engelter S, Grond-Ginsbach C. Familial cervical artery dissections: clinical, morphologic, and genetic studies. Stroke. 37: 2924-9. PMID 17053184 DOI: 10.1161/01.STR.0000248916.52976.49 |
0.127 |
|
| 1995 |
Eyskens F, Ceuterick C, Martin JJ, Janssens G, Jaeken J. Carbohydrate-deficient glycoprotein syndrome with previously unreported features. Acta Paediatrica (Oslo, Norway : 1992). 83: 892-6. PMID 7981572 DOI: 10.1111/j.1651-2227.1994.tb13166.x |
0.126 |
|
| 1992 |
Van de Kelft E, De Boulle K, Willems P, Martin JJ, Selosse P, Van der Auwera B. Loss of constitutional heterozygosity in human astrocytomas. Acta Neurochirurgica. 117: 172-7. PMID 1357919 DOI: 10.1007/BF01400616 |
0.126 |
|
| 2010 |
Le Bastard N, Martin JJ, Vanmechelen E, Vanderstichele H, De Deyn PP, Engelborghs S. Added diagnostic value of CSF biomarkers in differential dementia diagnosis. Neurobiology of Aging. 31: 1867-76. PMID 19150153 DOI: 10.1016/J.Neurobiolaging.2008.10.017 |
0.126 |
|
| 2016 |
De Paepe B, Martin JJ, Herbelet S, Jimenez-Mallebrera C, Iglesias E, Jou C, Weis J, De Bleecker JL. Activation of osmolyte pathways in inflammatory myopathy and Duchenne muscular dystrophy points to osmoregulation as a contributing pathogenic mechanism. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 27322952 DOI: 10.1038/labinvest.2016.68 |
0.126 |
|
| 2009 |
van der Zee J, Sleegers K, Vandenberghe R, Martin J, Engelborghs S, Sciot R, Mattheijssens M, De Deyn PP, Van Broeckhoven C, Crols R. O4-06-08: A multigenerational family with inherited, pathologically confirmed Creutzfeldt-Jakob disease unexplained by PRNP Alzheimer's & Dementia. 5: P164-P164. DOI: 10.1016/J.Jalz.2009.05.565 |
0.126 |
|
| 1987 |
Gahl WA, Finkelstein JD, Mullen KD, Bernardini I, Martin JJ, Backlund P, Ishak KG, Hoofnagle JH, Mudd SH. Hepatic methionine adenosyltransferase deficiency in a 31-year-old man. American Journal of Human Genetics. 40: 39-49. PMID 3812486 |
0.126 |
|
| 2005 |
Tilmont P, Louis J, Blanckaert D, Martin JJ, Morel P, Dubois B, Farriaux JP, Fontaine G. [Menkes disease. (A family case report)]. Annales De Pediatrie. 25: 333-40. PMID 16114343 |
0.125 |
|
| 1980 |
Debruyne J, Dehaene I, Martin JJ. Hereditary pressure-sensitive neuropathy. Journal of the Neurological Sciences. 47: 385-94. PMID 6932477 DOI: 10.1016/0022-510x(80)90091-x |
0.125 |
|
| 1971 |
Martin JJ, Deberdt R, Philippart M, Van Acker KJ, Hooft C. Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease. Acta Neuropathologica. 18: 224-33. PMID 5561979 DOI: 10.1007/BF00685068 |
0.125 |
|
| 1984 |
Neetens A, Martin JJ. Superior oblique myokymia in a case of hereditary metabolic neurodegenerative disease (adrenoleucodystrophy). Bulletin De La Societe Belge D'Ophtalmologie. 219-23. PMID 6675809 |
0.125 |
|
| 1999 |
Van Everbroeck B, Green AJ, Pals P, Martin JJ, Cras P. Decreased Levels of Amyloid-beta 1-42 in Cerebrospinal Fluid of Creutzfeldt-Jakob Disease Patients. Journal of Alzheimer's Disease : Jad. 1: 419-424. PMID 12214117 DOI: 10.3233/Jad-1999-1606 |
0.125 |
|
| 1976 |
Martin JJ, Ceuterick C, Martin L, Leroy JG, Nuyts JP, Joris C. [Globoid cell leucodystrophy (Krabbe's disease). Peripheral nerve lesion (author's transl)]. Acta Neurologica Belgica. 74: 356-75. PMID 4377697 |
0.124 |
|
| 2004 |
Nettel B, Niranjan A, Martin JJ, Koebbe CJ, Kondziolka D, Flickinger JC, Lunsford LD. Gamma knife radiosurgery for trigeminal schwannomas. Surgical Neurology. 62: 435-444. PMID 15518853 DOI: 10.1016/J.Surneu.2004.02.035 |
0.124 |
|
| 1975 |
Radermecker FJ, Martin JJ, Kugler J, Stochdorph O. [Necrotizing herpetic encephalitis. Electro-clinical and pathological studies on two infantile cases (author's transl)]. Acta Neurologica Belgica. 75: 151-14. PMID 169665 |
0.123 |
|
| 2005 |
Kondziolka D, Martin JJ, Flickinger JC, Friedland DM, Brufsky AM, Baar J, Agarwala S, Kirkwood JM, Lunsford LD. Long-term survivors after gamma knife radiosurgery for brain metastases. Cancer. 104: 2784-91. PMID 16288488 DOI: 10.1002/Cncr.21545 |
0.123 |
|
| 2015 |
Gijselinck I, Van Mossevelde S, van der Zee J, Sieben A, Philtjens S, Heeman B, Engelborghs S, Vandenbulcke M, De Baets G, Bäumer V, Cuijt I, Van den Broeck M, Peeters K, Mattheijssens M, Rousseau F, ... ... Martin JJ, et al. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort. Neurology. PMID 26581300 DOI: 10.1212/Wnl.0000000000002220 |
0.123 |
|
| 1976 |
Farriaux JP, Dhondt JL, Formstecher P, Martin JJ, Pollitt RJ, Knit J, Lagrou A, Mardens Y, Fontaine G. [Pathological and biochemical studies on a neonatal case of argininosuccinic aciduria (author's transl)]. Acta Neurologica Belgica. 76: 26-34. PMID 961372 |
0.122 |
|
| 1978 |
De Mulder C, Martin JJ. [Adult metachromatic leucodystrophy (author's transl)]. Acta Neurologica Belgica. 78: 162-6. PMID 27055 |
0.122 |
|
| 1978 |
Martin JJ, Flament-Durand J, Farriaux JP, Buyssens N, Ketelbant-Balasse P, Jansen C. Menkes kinky-hair disease. A report on its pathology. Acta Neuropathologica. 42: 25-32. PMID 654875 DOI: 10.1007/BF01273263 |
0.121 |
|
| 2015 |
Niemantsverdriet E, Goossens J, Struyfs H, Martin J, Goeman J, De Deyn PP, Vanderstichele HM, Engelborghs S. O4-11-03: Limited impact of CSF biomarkers variability on clinical diagnosis in autopsy-confirmed Alzheimer's disease Alzheimer's & Dementia. 11: P296-P297. DOI: 10.1016/J.Jalz.2015.07.407 |
0.121 |
|
| 2016 |
Niemantsverdriet E, Goossens J, Struyfs H, Martin JJ, Goeman J, De Deyn PP, Vanderstichele H, Engelborghs S. Diagnostic Impact of Cerebrospinal Fluid Biomarker (Pre-)Analytical Variability in Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. 51: 97-106. PMID 26836187 DOI: 10.3233/Jad-150953 |
0.121 |
|
| 1985 |
Martin JJ, Cras P. Familial erythrophagocytic lymphohistiocytosis. A neuropathologic study. Acta Neuropathologica. 66: 140-4. PMID 4013668 DOI: 10.1007/BF00688689 |
0.12 |
|
| 2015 |
Niemantsverdriet E, Feyen BF, Le Bastard N, Martin JJ, Goeman J, De Deyn PP, Engelborghs S. Overdiagnosing Vascular Dementia using Structural Brain Imaging for Dementia Work-Up. Journal of Alzheimer's Disease : Jad. 45: 1039-43. PMID 25633672 DOI: 10.3233/Jad-142103 |
0.12 |
|
| 2022 |
Laton J, Van Schependom J, Goossens J, Wiels W, Sieben A, De Deyn PP, Goeman J, Streffer J, van der Zee J, Martin JJ, Van Broeckhoven C, De Vos M, Bjerke M, Nagels G, Engelborghs S. Improved Alzheimer's Disease versus Frontotemporal Lobar Degeneration Differential Diagnosis Combining EEG and Neurochemical Biomarkers: A Pilot Study. Journal of Alzheimer's Disease : Jad. 90: 1739-1747. PMID 36336933 DOI: 10.3233/JAD-220693 |
0.118 |
|
| 1994 |
Lübke U, Six J, Villanova M, Boons J, Vandermeeren M, Ceuterick C, Cras P, Martin JJ. Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disorders. The American Journal of Pathology. 145: 175-88. PMID 7518193 |
0.118 |
|
| 1966 |
Gaburro D, Martin JJ, Scarpa P, Volpato S. [Congenital form of familial spongy degeneration]. Revue Neurologique. 112: 15-29. PMID 5855546 |
0.118 |
|
| 1982 |
Martin JJ, Dehaene I, Shiraki H. [Grumose alteration of the cerebellar dentate nucleus in two cases of progressive supranuclear palsy (author's transl)]. Acta Neurologica Belgica. 81: 137-43. PMID 7304125 |
0.117 |
|
| 1997 |
Van den Bergh PY, Guettat L, Vande Berg BC, Martin JJ. Focal myopathy associated with chronic intramuscular injection of piritramide. Muscle & Nerve. 20: 1598-600. PMID 9390676 DOI: 10.1002/(sici)1097-4598(199712)20:12<1598::aid-mus18>3.0.co;2-x |
0.117 |
|
| 1969 |
Guazzi GC, Martin JJ, Brucher JM, Taper HS, Macken J, Neethens A, Van Haegenborgh J. [On the significance of vascular involvement and glial dystrophy in Leigh's necrosing encephalomyelopathy. Study of 2 families and 3 anatomic cases]. Journal of the Neurological Sciences. 7: 357-79. PMID 5707083 DOI: 10.1016/0022-510x(68)90155-x |
0.117 |
|
| 1974 |
Martin JJ, Van Dessel G, Lagrou A, De Barsy AM, Dierick W. Multiple system atrophies. A neuropathological and neurochemical study. Journal of the Neurological Sciences. 21: 251-72. PMID 4361662 DOI: 10.1016/0022-510x(74)90171-3 |
0.117 |
|
| 1981 |
Juillet Y, Blanchard J, Martin JJ, Dubois C, Fiessinger JN, Cormer JM, Housset E. [Evaluation of the spread of atherosclerosis in patients with arteritis. Implications for the therapeutic indications (author's transl)]. Journal Des Maladies Vasculaires. 6: 10-12. PMID 7288297 |
0.117 |
|
| 2013 |
Le Bastard N, Coart E, Vanderstichele H, Vanmechelen E, Martin JJ, Engelborghs S. Comparison of two analytical platforms for the clinical qualification of Alzheimer's disease biomarkers in pathologically-confirmed dementia. Journal of Alzheimer's Disease : Jad. 33: 117-31. PMID 22936010 DOI: 10.3233/Jad-2012-121246 |
0.116 |
|
| 1969 |
Oud JS, Henneman IP, Brugge RJ, Hariga J, Martin JJ. [Leber's disease. Anatomic study of 2 cases in brothers]. Journal of the Neurological Sciences. 6: 401-17. PMID 5710144 DOI: 10.1016/0022-510x(68)90027-0 |
0.116 |
|
| 1999 |
Lipschutz W, Cadranel S, Lipschutz B, Martin L, Clees N, Martin JJ, Wauters JG, Coucke P, Willems P. 18q-syndrome with coeliac disease. European Journal of Pediatrics. 158: 528. PMID 10378408 DOI: 10.1007/s004310051137 |
0.116 |
|
| 1998 |
Keersmaekers A, Truyen L, Ramon F, Cras P, De Clerck L, Martin JJ. Cervical myelopathy due to rheumatoid arthritis. Case report and review of the literature. Acta Neurologica Belgica. 98: 284-8. PMID 9801709 |
0.115 |
|
| 2000 |
Wynants H, Taelman H, Martin JJ, Van den Ende J. Recurring aseptic meningitis after travel to the tropics: a case of Mollaret's meningitis? Case report with review of the literature. Clinical Neurology and Neurosurgery. 102: 113-5. PMID 10817900 DOI: 10.1016/S0303-8467(00)00074-3 |
0.115 |
|
| 2010 |
Chen CC, Engelborghs S, Dewaele S, Le Bastard N, Martin JJ, Vanhooren V, Libert C, De Deyn PP. Altered serum glycomics in Alzheimer disease: a potential blood biomarker? Rejuvenation Research. 13: 439-44. PMID 20426627 DOI: 10.1089/Rej.2009.0992 |
0.115 |
|
| 1969 |
De Barsy T, Myle G, Troch C, Matthys R, Martin JJ. [Myoclonic cerebellar dyssynergy (R. Hunt): autonomic disease or variation of the progressive degenerative epilepsy-myoclonus (Unverricht-Lundberg). Anatomo-clinical approach]. Journal of the Neurological Sciences. 8: 111-27. PMID 5790364 DOI: 10.1016/0022-510x(69)90045-8 |
0.115 |
|
| 1992 |
Timmerman V, Raeymaekers P, Nelis E, De Jonghe P, Muylle L, Ceuterick C, Martin JJ, Van Broeckhoven C. Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree Journal of the Neurological Sciences. 109: 41-48. PMID 1517763 DOI: 10.1016/0022-510X(92)90091-X |
0.114 |
|
| 1993 |
Vandermeeren M, Mercken M, Vanmechelen E, Six J, van de Voorde A, Martin JJ, Cras P. Detection of tau proteins in normal and Alzheimer's disease cerebrospinal fluid with a sensitive sandwich enzyme-linked immunosorbent assay. Journal of Neurochemistry. 61: 1828-34. PMID 8228996 DOI: 10.1111/J.1471-4159.1993.Tb09823.X |
0.114 |
|
| 1998 |
Zukowski F, De Craemer D, Van den Branden C, De Cauwer H, Heytens L, Martin JJ. An image analysis study of vastus lateralis muscle fibers in malignant hyperthermia susceptible patients. Clinical Neuropathology. 17: 6-11. PMID 9496533 |
0.114 |
|
| 2008 |
Engelborghs S, De Vreese K, Van de Casteele T, Vanderstichele H, Van Everbroeck B, Cras P, Martin JJ, Vanmechelen E, De Deyn PP. Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia. Neurobiology of Aging. 29: 1143-59. PMID 17428581 DOI: 10.1016/j.neurobiolaging.2007.02.016 |
0.114 |
|
| 1993 |
Villanova M, Kawai M, Lübke U, Oh SJ, Perry G, Six J, Ceuterick C, Martin JJ, Cras P. Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markers. Brain Research. 603: 343-7. PMID 8461987 DOI: 10.1016/0006-8993(93)91260-Y |
0.114 |
|
| 2016 |
Vermeiren Y, Janssens J, Aerts T, Martin JJ, Sieben A, Van Dam D, De Deyn PP. Brain Serotonergic and Noradrenergic Deficiencies in Behavioral Variant Frontotemporal Dementia Compared to Early-Onset Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 27314528 DOI: 10.3233/JAD-160320 |
0.113 |
|
| 1994 |
Hanemann CO, Stoll G, D'Urso D, Fricke W, Martin JJ, Van Broeckhoven C, Mancardi GL, Bartke I, Müller HW. Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies. Journal of Neuroscience Research. 37: 654-9. PMID 8028042 DOI: 10.1002/jnr.490370513 |
0.113 |
|
| 1998 |
Hendriks L, De Jonghe C, Lübke U, Woodrow S, Vanderhoeven I, Boons J, Cras P, Martin JJ, Van Broeckhoven C. Immunoreactivity of presenilin-1 and tau in Alzheimer's disease brain. Experimental Neurology. 149: 341-8. PMID 9500965 DOI: 10.1006/exnr.1997.6739 |
0.113 |
|
| 2013 |
Martin JJ. Ptosis repair in aesthetic blepharoplasty. Clinics in Plastic Surgery. 40: 201-12. PMID 23186770 DOI: 10.1016/j.cps.2012.06.007 |
0.112 |
|
| 1981 |
Martin JJ, Leroy JG, Ceuterick C, Libert J, Dodinval P, Martin L. Fetal Krabbe leukodystrophy. A morphologic study of two cases. Acta Neuropathologica. 53: 87-91. PMID 7211207 DOI: 10.1007/BF00689987 |
0.112 |
|
| 1991 |
Abs R, Van Vleymen E, Parizel PM, Van Acker K, Martin M, Martin JJ. Congenital cerebellar hypoplasia and hypogonadotropic hypogonadism. Journal of the Neurological Sciences. 98: 259-65. PMID 2243234 DOI: 10.1016/0022-510x(90)90267-q |
0.112 |
|
| 2010 |
Van Craenenbroeck A, Gebruers M, Martin JJ, Cras P. Hallervorden-Spatz disease: historical case presentation in the spotlight of nosological evolution. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 2486-92. PMID 20721923 DOI: 10.1002/mds.23217 |
0.112 |
|
| 2004 |
Van Everbroeck B, Dobbeleir I, De Waele M, De Leenheir E, Lübke U, Martin JJ, Cras P. Extracellular protein deposition correlates with glial activation and oxidative stress in Creutzfeldt-Jakob and Alzheimer's disease. Acta Neuropathologica. 108: 194-200. PMID 15221335 DOI: 10.1007/s00401-004-0879-2 |
0.112 |
|
| 1995 |
De Deyn PP, Ceuterick C, Saxena V, Crols R, Chappel R, Martin JJ. Chronic colchicine-induced myopathy and neuropathy. Acta Neurologica Belgica. 95: 29-32. PMID 7725894 |
0.111 |
|
| 1979 |
Martin JJ, Leroy JG, Libert J, van Eygen M, Logghe N. Skin and conjunctival biopsies in infantile neuroaxonal dystrophy. Acta Neuropathologica. 45: 247-51. PMID 442990 DOI: 10.1007/BF00702677 |
0.111 |
|
| 2010 |
Claeys KG, Sozanska M, Martin JJ, Lacene E, Vignaud L, Stockholm D, Laforêt P, Eymard B, Kichler A, Scherman D, Voit T, Israeli D. DNAJB2 expression in normal and diseased human and mouse skeletal muscle. The American Journal of Pathology. 176: 2901-10. PMID 20395441 DOI: 10.2353/ajpath.2010.090663 |
0.111 |
|
| 1986 |
Griffiths JD, Ding JC, Juneja SK, Thomas RJ, Martin JJ, Cooper IA. Pathological rupture of the spleen in transforming non-Hodgkin's lymphoma. The Medical Journal of Australia. 144: 146-7, 150. PMID 3753741 DOI: 10.5694/j.1326-5377.1986.tb112245.x |
0.11 |
|
| 2006 |
Wiest T, Hyrenbach S, Bambul P, Erker B, Pezzini A, Hausser I, Arnold ML, Martin JJ, Engelter S, Lyrer P, Busse O, Brandt T, Grond-Ginsbach C. Genetic analysis of familial connective tissue alterations associated with cervical artery dissections suggests locus heterogeneity. Stroke; a Journal of Cerebral Circulation. 37: 1697-702. PMID 16728685 DOI: 10.1161/01.STR.0000226624.93519.78 |
0.11 |
|
| 1996 |
van den Hauwe L, Parizel PM, Van Goethem JW, Cras P, Martin JJ, Dieleman-Smet H, De Schepper AM. Parinaud's syndrome in a patient with multifocal glioma. Journal Belge De Radiologie. 79: 20-2. PMID 8647784 |
0.11 |
|
| 1969 |
Jansseune H, Philippart M, Martin JJ. [On 2 cases of Niemann-Pick disease. Chronic form with delayed neurologic involvement]. Acta Paediatrica Belgica. 21: 239-52. PMID 5614330 |
0.11 |
|
| 1981 |
Ceuterick C, Martin JJ, Libert J, Farriaux JP. Sanfilippo A disease in the fetus--comparison with pre- and postnatal cases. Neuropadiatrie. 11: 176-85. PMID 6777713 DOI: 10.1055/s-2008-1071387 |
0.11 |
|
| 2013 |
Le Bastard N, Aerts L, Sleegers K, Martin JJ, Van Broeckhoven C, De Deyn PP, Engelborghs S. Longitudinal stability of cerebrospinal fluid biomarker levels: fulfilled requirement for pharmacodynamic markers in Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 33: 807-22. PMID 23034521 DOI: 10.3233/JAD-2012-110029 |
0.109 |
|
| 1990 |
Roodhooft AM, Baumgartner ER, Martin JJ, Blom W, Van Acker KJ. Symmetrical necrosis of the basal ganglia in methylmalonic acidaemia. European Journal of Pediatrics. 149: 582-4. PMID 2189733 DOI: 10.1007/BF01957698 |
0.109 |
|
| 1976 |
Ceuterick Ch, Martin JJ, Casaer P, Edgar GW. The diagnosis of infantile generalized ceroidlipofuscinosis (type Hagberg-Santavuori) using skin biopsy. Neuropadiatrie. 7: 250-60. PMID 183172 DOI: 10.1055/s-0028-1091627 |
0.109 |
|
| 1975 |
Martin JJ, Leroy JG, Farriaux JP, Fontaine G, Desnick RJ, Cabello A. I-cell disease (mucolipidosis II):a report on its pathology. Acta Neuropathologica. 33: 285-305. PMID 3084 DOI: 10.1007/Bf00686161 |
0.109 |
|
| 1972 |
Palladini G, Martin JJ. [Histochemical study of muscular basophil substances in Pompe's disease]. Acta Neurologica. 27: 140-2. PMID 4261280 |
0.108 |
|
| 1998 |
MARTIN JJ. [The cerebellar lesions of von Recklinghausen's neurofibromatosis. Apropos of a clinical case]. Acta Neurologica Et Psychiatrica Belgica. 61: 1117-38. PMID 14470399 |
0.108 |
|
| 1993 |
Mertens G, Ieven M, Ursi D, Pattyn SR, Martin JJ, Parizel PM. Detection of herpes simplex virus in the cerebrospinal fluid of patients with encephalitis using the polymerase chain reaction Journal of the Neurological Sciences. 118: 213-216. PMID 8229072 DOI: 10.1016/0022-510X(93)90113-D |
0.108 |
|
| 1976 |
Martin JJ, Ceuterick Ch, Edgar GW. [Infantile generalized ceroid-Lipofuscinosis (type Hagberg-Santavuori). A new case and a retrospective study of two observations (author's transl)]. Acta Neurologica Belgica. 76: 103-22. PMID 183451 |
0.108 |
|
| 2015 |
Slaets S, Van Acker F, Versijpt J, Hauth L, Goeman J, Martin JJ, De Deyn PP, Engelborghs S. Diagnostic value of MIBG cardiac scintigraphy for differential dementia diagnosis. International Journal of Geriatric Psychiatry. 30: 864-9. PMID 25363642 DOI: 10.1002/Gps.4229 |
0.107 |
|
| 2007 |
Martin JJ, Kondziolka D, Flickinger JC, Mathieu D, Niranjan A, Lunsford LD. Cranial nerve preservation and outcomes after stereotactic radiosurgery for jugular foramen schwannomas. Neurosurgery. 61: 76-81; discussion 81. PMID 17621021 DOI: 10.1227/01.Neu.0000279726.90650.6D |
0.106 |
|
| 1996 |
Villanova M, Malandrini A, Toti P, Salvestroni R, Six J, Martin JJ, Guazzi GC. Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency. Journal of Submicroscopic Cytology and Pathology. 28: 1-4. PMID 8929621 |
0.105 |
|
| 1990 |
Cras P, Ceuterick-de Groote C, Van Vyve M, Vercruyssen A, Martin JJ. Malignant pigmented spinal nerve root schwannoma metastasizing in the brain and viscera. Clinical Neuropathology. 9: 290-4. PMID 2286020 |
0.105 |
|
| 1982 |
Juillet Y, Blanchard J, Martin JJ, Dubois C, Fiessinger JN, Cormier JM, Housset E. [Diffusion of atherosclerosis in patients with arterial disease of the lower limbs (author's transl)]. Annales De Medecine Interne. 132: 252-6. PMID 7305174 |
0.105 |
|
| 1980 |
Neetens A, Libert J, Martin JJ, Leroy JG. Cherry red spot-ataxia-myoclonus. Bulletin De La Societe Belge D'Ophtalmologie. 185: 67-76. PMID 540193 |
0.104 |
|
| 2016 |
Somers C, Struyfs H, Goossens J, Niemantsverdriet E, Luyckx J, De Roeck N, De Roeck E, De Vil B, Cras P, Martin JJ, De Deyn PP, Bjerke M, Engelborghs S. A Decade of Cerebrospinal Fluid Biomarkers for Alzheimer's Disease in Belgium. Journal of Alzheimer's Disease : Jad. 54: 383-95. PMID 27567807 DOI: 10.1016/J.Jalz.2016.06.918 |
0.104 |
|
| 1983 |
Vercruyssen A, Martin JJ, Ceuterick C, Jacobs K, Swerts L. Adult ceroid-lipofuscinosis: diagnostic value of biopsies and of neurophysiological investigations. Journal of Neurology, Neurosurgery, and Psychiatry. 45: 1056-9. PMID 6294251 DOI: 10.1136/jnnp.45.11.1056 |
0.104 |
|
| 1985 |
Martin JJ. Hereditary metabolic disorders affecting myelin. Bulletin De La Societe Belge D'Ophtalmologie. 208: 11-8. PMID 6681112 |
0.104 |
|
| 1997 |
de Deyn PP, Martin JJ. [The loss of autonomy in disabling neurologic diseases. Ethical considerations]. Revue Medicale De Liege. 52: 403-12. PMID 9289772 |
0.104 |
|
| 2000 |
Finkelstein JD, Martin JJ. Homocysteine. The International Journal of Biochemistry & Cell Biology. 32: 385-9. PMID 10762063 DOI: 10.1016/s1357-2725(99)00138-7 |
0.104 |
|
| 1982 |
Martin JJ, Farriaux JP, De Jonghe P. Neuropathology of citrullinaemia. Acta Neuropathologica. 56: 303-6. PMID 7090738 DOI: 10.1007/BF00691263 |
0.104 |
|
| 1994 |
Villanova M, De Clerck LS, Cras P, Guazzi GC, Martin JJ. Eosinophilia myalgia syndrome: absence of immunoglobulin reactivity suggests a cellular rather than humoral mechanism. Acta Neurologica Belgica. 94: 200-4. PMID 7976226 |
0.104 |
|
| 2016 |
Goossens J, Laton J, Van Schependom J, Gielen J, Struyfs H, Van Mossevelde S, Van den Bossche T, Goeman J, De Deyn PP, Sieben A, Martin JJ, Van Broeckhoven C, van der Zee J, Engelborghs S, Nagels G. EEG Dominant Frequency Peak Differentiates Between Alzheimer's Disease and Frontotemporal Lobar Degeneration. Journal of Alzheimer's Disease : Jad. PMID 27636837 DOI: 10.1016/J.Jalz.2016.06.656 |
0.103 |
|
| 2014 |
Struyfs H, Molinuevo JL, Martin JJ, De Deyn PP, Engelborghs S. Validation of the AD-CSF-index in autopsy-confirmed Alzheimer's disease patients and healthy controls. Journal of Alzheimer's Disease : Jad. 41: 903-9. PMID 24705548 DOI: 10.3233/Jad-131085 |
0.103 |
|
| 1983 |
Martin JJ, Mercelis R, Dua G, Moens E. Bulbo-spinal lower motor neuron disease. Accumulation of neurofilaments in perikarya and axons. Acta Neurologica Belgica. 82: 262-9. PMID 6890751 |
0.103 |
|
| 2014 |
Slaets S, Vanmechelen E, Le Bastard N, Decraemer H, Vandijck M, Martin JJ, De Deyn PP, Engelborghs S. Increased CSF α-synuclein levels in Alzheimer's disease: correlation with tau levels. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: S290-8. PMID 24439167 DOI: 10.1016/J.Jalz.2013.10.004 |
0.102 |
|
| 1972 |
Martinez-Lage JM, Martin JJ. [Pluricentric systematic extensions of reticular atrophy of the central nervous system, their clinical polymorphism, and relationship to paraneoplastic changes of the central nervous system]. Acta Neurologica Belgica. 72: 39-53. PMID 5024248 |
0.102 |
|
| 1967 |
van Bogaert L, van Mechelen P, Martin JJ, Guazzi GC. [On the neuropathology of Refsum-Thiébaut disease. (Memorandum on the observation of Richterich, Kahlke, van Mechelen and Rossi, 1963)]. Revue Neurologique. 116: 229-40. PMID 4167758 |
0.102 |
|
| 1979 |
Van Dessel G, Lagrou A, Martin JJ, Ceuterick C, Dierick W. Two cases of mucopolysaccharidosis type III (Sanfilippo). A biochemical study. Journal of the Neurological Sciences. 40: 77-86. PMID 107278 DOI: 10.1016/0022-510x(79)90193-x |
0.102 |
|
| 1969 |
Philippart M, Martin L, Martin JJ, Menkes JH. Niemann-Pick disease. Morphologic and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C). Archives of Neurology. 20: 227-38. PMID 5766485 DOI: 10.1001/archneur.1969.00480090015001 |
0.101 |
|
| 1998 |
Toti P, De Felice C, Palmeri ML, Villanova M, Martín JJ, Buonocore G. Inflammatory pathogenesis of cortical polymicrogyria: an autopsy study. Pediatric Research. 44: 291-6. PMID 9727703 DOI: 10.1203/00006450-199809000-00005 |
0.101 |
|
| 1979 |
Martin JJ, Ceuterick C, Van Dessel G, Lagrou A, Dierick W. Two cases of mucopolysaccharidosis type III (Sanfilippo). An anatomopathological study. Acta Neuropathologica. 46: 185-90. PMID 223363 DOI: 10.1007/BF00690842 |
0.101 |
|
| 2006 |
Moreno-Ramirez D, Ferrandiz L, Bernal AP, Duran RC, Martín JJ, Camacho F. Teledermatology as a filtering system in pigmented lesion clinics. Journal of Telemedicine and Telecare. 11: 298-303. PMID 16168166 DOI: 10.1258/1357633054893364 |
0.1 |
|
| 2006 |
De Vriese AS, Coster RV, Smet J, Seneca S, Lovering A, Van Haute LL, Vanopdenbosch LJ, Martin JJ, Groote CC, Vandecasteele S, Boelaert JR. Linezolid-induced inhibition of mitochondrial protein synthesis. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 42: 1111-7. PMID 16575728 DOI: 10.1086/501356 |
0.1 |
|
| 1968 |
Bouteille M, Guazii GC, Martin JJ, Masselin S, Houdart R, Delarue J. [A case of Schilder's diffuse encephalitis periaxialis. I. Anatomo-clinical study]. Annales D'Anatomie Pathologique. 13: 43-54. PMID 4299873 |
0.1 |
|
| 1999 |
Villanova M, Ceuterick C, Dotti MT, Santorelli FM, Casali C, Malandrini A, De Stefano N, Lübke U, Martin JJ, Guazzi GC, Federico A. Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren). Acta Neuropathologica. 98: 78-84. PMID 10412803 DOI: 10.1007/s004010051053 |
0.1 |
|
| 2009 |
Kondziolka D, Madhok R, Lunsford LD, Mathieu D, Martin JJ, Niranjan A, Flickinger JC. Stereotactic radiosurgery for convexity meningiomas. Journal of Neurosurgery. 111: 458-63. PMID 19199473 DOI: 10.3171/2008.8.Jns17650 |
0.099 |
|
| 2009 |
De Paepe B, Creus KK, Martin JJ, Weis J, De Bleecker JL. A dual role for HSP90 and HSP70 in the inflammatory myopathies: from muscle fiber protection to active invasion by macrophages. Annals of the New York Academy of Sciences. 1173: 463-9. PMID 19758187 DOI: 10.1111/j.1749-6632.2009.04812.x |
0.099 |
|
| 2003 |
Pals P, Van Everbroeck B, Grubben B, Viaene MK, Dom R, van der Linden C, Santens P, Martin JJ, Cras P. Case-control study of environmental risk factors for Parkinson's disease in Belgium. European Journal of Epidemiology. 18: 1133-42. PMID 14758870 DOI: 10.1023/B:EJEP.0000006639.05690.92 |
0.099 |
|
| 1984 |
Martin JJ. Mechanisms of demyelination in hereditary metabolic disorders. Bulletin De La Societe Belge D'Ophtalmologie. 109-11. PMID 6675799 |
0.099 |
|
| 2014 |
Bridet L, Martin JJ, Nuno JL. Acute liver damage and anorexia nervosa: a case report. The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology. 25: 205-8. PMID 25003683 DOI: 10.5152/tjg.2014.2531 |
0.099 |
|
| 2001 |
Deprez M, Ceuterick-de Groote C, Schoenen J, Reznik M, Martin JJ. Nerve biopsy: indications and contribution to the diagnosis of peripheral neuropathy. The experience of the Born Bunge Foundation University of Antwerp and University of Liege between 1987 and 1997. Acta Neurologica Belgica. 100: 162-6. PMID 11098289 |
0.098 |
|
| 1977 |
Kugler J, Martin JJ, Radermecker FJ, Stochdorph O. [Periodicity complexes in the EEG of necrotising herpes-encephalitis (author's transl)]. Eeg-Emg Zeitschrift Fur Elektroenzephalographie, Elektromyographie Und Verwandte Gebiete. 7: 63-71. PMID 829050 |
0.098 |
|
| 1979 |
Den Tandt WR, Martin JJ. Peroxidase in ceroid-lipofuscinosis. Journal of the Neurological Sciences. 38: 191-3. PMID 712383 DOI: 10.1016/0022-510x(78)90065-5 |
0.098 |
|
| 1989 |
Roosen N, Cras P, Paquier P, Martin JJ. Primary thalamic malignant fibrous histiocytoma of the dominant hemisphere causing severe neuropsychological symptoms. Clinical Neuropathology. 8: 16-21. PMID 2539933 |
0.097 |
|
| 1993 |
Mulkens TH, Parizel PM, De Schepper AM, van de Heyning PH, Forton GE, Martin JJ, Delaporte C. MRI of acoustic schwannoma: a retrospective study of 89 tumours. RöFo : Fortschritte Auf Dem Gebiete Der RöNtgenstrahlen Und Der Nuklearmedizin. 158: 362-7. PMID 8477078 DOI: 10.1055/S-2008-1032664 |
0.097 |
|
| 2013 |
Slaets S, Le Bastard N, Theuns J, Sleegers K, Verstraeten A, De Leenheir E, Luyckx J, Martin JJ, Van Broeckhoven C, Engelborghs S. Amyloid pathology influences aβ1-42 cerebrospinal fluid levels in dementia with lewy bodies. Journal of Alzheimer's Disease : Jad. 35: 137-46. PMID 23364139 DOI: 10.3233/Jad-122176 |
0.097 |
|
| 2011 |
Slaets S, Engelborghs S, Le Bastard N, De Deyn P, De Leenheir E, Luyckx J, Martin J. P1-113: Influence of AD pathology on CSF biomarkers in autopsy-confirmed Dementia with Lewy Bodies patients Alzheimer's & Dementia. 7: S146-S146. DOI: 10.1016/J.Jalz.2011.05.392 |
0.096 |
|
| 2018 |
Goossens J, Bjerke M, Van Mossevelde S, Van den Bossche T, Goeman J, De Vil B, Sieben A, Martin JJ, Cras P, De Deyn PP, Van Broeckhoven C, van der Zee J, Engelborghs S. Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration. Alzheimer's Research & Therapy. 10: 31. PMID 29559004 DOI: 10.1186/S13195-018-0364-0 |
0.096 |
|
| 2000 |
Chappel R, Willems J, Martin JJ. Charcot joint in idiopathic sensorimotor neuropathy. Clinical Rheumatology. 19: 153-5. PMID 10791630 DOI: 10.1007/s100670050036 |
0.095 |
|
| 1971 |
Martin JJ. [Anatomy of the thalamus and its pathology in degenerative diseases designated as abiotrophic]. Acta Neurologica Belgica. 70: 5-211. PMID 4255565 |
0.095 |
|
| 2007 |
Martin JJ, Niranjan A, Kondziolka D, Flickinger JC, Lozanne KA, Lunsford LD. Radiosurgery for chordomas and chondrosarcomas of the skull base Journal of Neurosurgery. 107: 758-764. PMID 17937220 DOI: 10.3171/Jns-07/10/0758 |
0.095 |
|
| 1988 |
Demey HE, Martin JJ, Leus RM, Moeremans CJ, Bossaert LL. Coma as a presenting sign of Epstein-Barr encephalitis. Archives of Internal Medicine. 148: 1459-61. PMID 2837158 |
0.095 |
|
| 2007 |
Engelborghs S, Sleegers K, Cras P, Brouwers N, Serneels S, De Leenheir E, Martin JJ, Vanmechelen E, Van Broeckhoven C, De Deyn PP. No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease. Brain : a Journal of Neurology. 130: 2320-6. PMID 17586559 DOI: 10.1093/Brain/Awm136 |
0.095 |
|
| 1967 |
Barraquer-Bordas L, Martin JJ, Ishino H, Milla-Santos J, Grau-Veciana JM, Bacci F. [On a thalamic necrosis with subacute meningo-ependymitis. Contribution to the study of psychic disorders of mesencephalothalamic origin]. Acta Neurologica Et Psychiatrica Belgica. 67: 7-24. PMID 4962821 |
0.094 |
|
| 2023 |
González S, Wall RJ, Thomas J, Braillard S, Brunori G, Camino Díaz I, Cantizani J, Carvalho S, Castañeda Casado P, Chatelain E, Cotillo I, Fiandor JM, Francisco AF, Grimsditch D, Keenan M, ... ... Martin JJ, et al. Short-course combination treatment for experimental chronic Chagas disease. Science Translational Medicine. 15: eadg8105. PMID 38091410 DOI: 10.1126/scitranslmed.adg8105 |
0.094 |
|
| 1994 |
Dierckx RA, Martin JJ, Dobbeleir A, Crols R, Neetens I, De Deyn PP. Sensitivity and specificity of thallium-201 single-photon emission tomography in the functional detection and differential diagnosis of brain tumours. European Journal of Nuclear Medicine. 21: 621-33. PMID 7957348 DOI: 10.1007/BF00285584 |
0.094 |
|
| 2013 |
Izura V, Martin J, Herrero M. Impairment of autonomic nervous system in Parkinson's disease and its modulation Neurophysiologie Clinique/Clinical Neurophysiology. 43: 319-320. DOI: 10.1016/j.neucli.2013.10.021 |
0.094 |
|
| 1981 |
Martin JJ, Taylor ES. Diagnosis of bilateral hydronephrosis in utero by ultrasonography. Urology. 17: 272-3. PMID 7210380 DOI: 10.1016/0090-4295(81)90048-0 |
0.094 |
|
| 2004 |
Plaza V, Serrano J, Picado C, Cosano J, Ancochea J, de Diego A, Martín JJ, Sanchís J. [Clinical characteristics of the fatal and near-fatal asthma in Alternaria alternata sensitized patients]. Medicina Clinica. 121: 721-4. PMID 14678692 DOI: 10.1016/s0025-7753(03)74076-7 |
0.094 |
|
| 1989 |
Neetens A, Martin JJ, Neetens I, Smets RM. The Klippel-Trenaunay-Sturge-Weber syndrome. Bulletin De La Societe Belge D'Ophtalmologie. 224: 123-37. PMID 2855036 |
0.094 |
|
| 1997 |
Martin JJ, Ceuterick C. Adult neuronal ceroid-lipofuscinosis--personal observations. Acta Neurologica Belgica. 97: 85-92. PMID 9246375 |
0.093 |
|
| 2018 |
Niemantsverdriet E, Feyen BFE, Le Bastard N, Martin JJ, Goeman J, De Deyn PP, Bjerke M, Engelborghs S. Added Diagnostic Value of Cerebrospinal Fluid Biomarkers for Differential Dementia Diagnosis in an Autopsy-Confirmed Cohort. Journal of Alzheimer's Disease : Jad. PMID 29614653 DOI: 10.3233/Jad-170927 |
0.093 |
|
| 1982 |
Van Zandycke M, Martin JJ, Vande Gaer L, Van den Heyning P. Facial myokymia in the Guillain-Barré syndrome: a clinicopathologic study. Neurology. 32: 744-8. PMID 7201111 DOI: 10.1212/wnl.32.7.744 |
0.092 |
|
| 1984 |
Martin JJ. Hereditary metabolic myelin diseases in humans. Bulletin De La Societe Belge D'Ophtalmologie. 375-98. PMID 6675823 |
0.092 |
|
| 1978 |
Verougstraete C, Libert J, Martin JJ, Danis P. [Ocular ultrastructural studies in ceroid lipfuscinosis: preliminary note]. Bulletin De La Societe Belge D'Ophtalmologie. 27-35. PMID 614086 |
0.092 |
|
| 1988 |
Gahl WA, Bernardini I, Finkelstein JD, Tangerman A, Martin JJ, Blom HJ, Mullen KD, Harvey Mudd S. Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency Journal of Clinical Investigation. 81: 390-397. PMID 3339126 DOI: 10.1172/Jci113331 |
0.092 |
|
| 1969 |
Stoupel N, Monseu G, Pardoe A, Heimann R, Martin JJ. Encephalitis with myoclonus in Whipple's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 32: 338-43. PMID 4185341 DOI: 10.1136/jnnp.32.4.338 |
0.092 |
|
| 1974 |
Neimann N, Vidailhet M, Martin JJ, Andre M, Floquet J, Grignon J. [Bone fragility, amyotrophy, mental retardation and degenerative lesions of the central nervous system. A new familial disorder]. Archives Francaises De Pediatrie. 30: 899-913. PMID 4799972 |
0.092 |
|
| 1984 |
Martin JJ, Lowenthal A, Ceuterick C, Vanier MT. Juvenile dystonic lipidosis (variant of Niemann-Pick disease type C). Journal of the Neurological Sciences. 66: 33-45. PMID 6520612 |
0.091 |
|
| 2017 |
Traenka C, Dougoud D, Simonetti BG, Metso TM, Debette S, Pezzini A, Kloss M, Grond-Ginsbach C, Majersik JJ, Worrall BB, Leys D, Baumgartner R, Caso V, Béjot Y, Compter A, ... ... Martin JJ, et al. Cervical artery dissection in patients ≥60 years: Often painless, few mechanical triggers. Neurology. PMID 28258079 DOI: 10.1212/WNL.0000000000003788 |
0.091 |
|
| 1973 |
Leroy JG, Van Elsen AF, Martin JJ, Dumon JE, Hulet AE, Okada S, Navarro C. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis. The New England Journal of Medicine. 288: 1365-9. PMID 4707419 DOI: 10.1056/NEJM197306282882602 |
0.091 |
|
| 1968 |
Bogaert LV, Kissel P, Schmitt J, Martin JJ, Claes C, Duc M, Royer R, Barrucand D, Grignon G, Floquet J. [Adynamia episodica hereditaria. Study of 2 familial cases]. Journal of the Neurological Sciences. 5: 543-54. PMID 6073217 DOI: 10.1016/0022-510x(67)90091-3 |
0.091 |
|
| 1968 |
Philippart M, Martin L, Martin JJ. Glycolipid alterations in Niemann-Pick disease (Crocker type C). Neurology. 18: 301. PMID 5690403 |
0.09 |
|
| 2019 |
Pfeiffer D, Chen B, Schlicht K, Ginsbach P, Abboud S, Bersano A, Bevan S, Brandt T, Caso V, Debette S, Erhart P, Freitag-Wolf S, Giacalone G, Grau AJ, Hayani E, ... ... Martin JJ, et al. Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke. Stroke. STROKEAHA118021856. PMID 30661490 DOI: 10.1161/Strokeaha.118.021856 |
0.09 |
|
| 1985 |
Roosen N, Martin JJ, de la Porte C, Van Vyve M. Intracerebral hemorrhage due to cerebral amyloid angiopathy. Case report. Journal of Neurosurgery. 63: 965-9. PMID 4056911 DOI: 10.3171/jns.1985.63.6.0965 |
0.09 |
|
| 1992 |
Hutchinson ML, Isenstein LM, Martin JJ, Zahniser DJ. Measurement of subvisual changes in cervical squamous metaplastic cells for detecting abnormality Analytical and Quantitative Cytology and Histology. 14: 330-334. PMID 1388570 |
0.09 |
|
| 1993 |
Bosmans J, Degryse H, Martin JJ, De Schepper A. Steinert's disease Journal Belge De Radiologie. 76: 28. PMID 8320190 |
0.089 |
|
| 1969 |
Guazzi GC, Martin JJ, Philippart M, Roels H, van der Eecken H, Vrints L, Delbeke MJ, Hooft C. Wolman's disease. European Neurology. 1: 334-62. PMID 5711398 DOI: 10.1159/000113673 |
0.089 |
|
| 1989 |
Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Martin JJ, Vandenberghe A. Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease. Human Genetics. 81: 231-3. PMID 2921030 DOI: 10.1007/BF00278994 |
0.089 |
|
| 1997 |
Decaestecker C, Lopes BS, Gordower L, Camby I, Cras P, Martin JJ, Kiss R, VandenBerg SR, Salmon I. Quantitative chromatin pattern description in Feulgen-stained nuclei as a diagnostic tool to characterize the oligodendroglial and astroglial components in mixed oligo-astrocytomas. Journal of Neuropathology and Experimental Neurology. 56: 391-402. PMID 9100670 DOI: 10.1097/00005072-199704000-00008 |
0.089 |
|
| 2017 |
Goossens J, Bjerke M, Struyfs H, Niemantsverdriet E, Somers C, Van den Bossche T, Van Mossevelde S, De Vil B, Sieben A, Martin JJ, Cras P, Goeman J, De Deyn PP, Van Broeckhoven C, van der Zee J, et al. No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis. Alzheimer's Research & Therapy. 9: 49. PMID 28709448 DOI: 10.1186/S13195-017-0275-5 |
0.089 |
|
| 1995 |
van den Hauwe L, Parizel PM, Martin JJ, Cras P, De Deyn P, De Schepper AM. Postmortem MRI of the brain with neuropathological correlation. Neuroradiology. 37: 343-9. PMID 7477830 DOI: 10.1007/BF00588007 |
0.089 |
|
| 1977 |
Neimann N, Martin JJ, Floquet J, Vidailhet M, Pierson M, Bajolle A. [Osseous fragility, amyotrophy, retarded development and degenerative lesions of the central nervous system. A new familial afflication]. Archives Francaises De Pediatrie. 33: 713-4. PMID 999442 |
0.089 |
|
| 2008 |
Kondziolka D, Mathieu D, Lunsford LD, Martin JJ, Madhok R, Niranjan A, Flickinger JC. Radiosurgery as definitive management of intracranial meningiomas. Neurosurgery. 62: 53-8; discussion 58-. PMID 18300891 DOI: 10.1227/01.Neu.0000311061.72626.0D |
0.088 |
|
| 2019 |
Roquero I, Cantizani J, Cotillo I, Manzano MP, Kessler A, Martín JJ, McNamara CW. Novel chemical starting points for drug discovery in leishmaniasis and Chagas disease. International Journal For Parasitology. Drugs and Drug Resistance. 10: 58-68. PMID 31158574 DOI: 10.1016/j.ijpddr.2019.05.002 |
0.088 |
|
| 1982 |
Martin JJ, Ceuterick C, Mercelis R, Joris C. Pathology of peripheral nerves in metachromatic leucodystrophy. A comparative study of ten cases. Journal of the Neurological Sciences. 53: 95-112. PMID 7057206 DOI: 10.1016/0022-510x(82)90084-3 |
0.088 |
|
| 2014 |
Lyrer PA, Brandt T, Metso TM, Metso AJ, Kloss M, Debette S, Leys D, Caso V, Pezzini A, Bonati LH, Thijs V, Bersano A, Touzé E, Gensicke H, Martin JJ, et al. Clinical import of Horner syndrome in internal carotid and vertebral artery dissection. Neurology. 82: 1653-9. PMID 24727317 DOI: 10.1212/WNL.0000000000000381 |
0.088 |
|
| 1984 |
Bruyland M, van Belle S, Schallier D, Ebinger G, Martin JJ. Good response of a paraneoplastic neuromyopathy to cyclophosphamide Cancer Treatment Reports. 68: 787-789. PMID 6327036 |
0.088 |
|
| 2021 |
Willemse EAJ, Sieben A, Somers C, Vermeiren Y, De Roeck N, Timmers M, Van Broeckhoven C, De Vil B, Cras P, De Deyn PP, Martin JJ, Teunissen CE, Engelborghs S, Bjerke M. Neurogranin as biomarker in CSF is non-specific to Alzheimer's disease dementia. Neurobiology of Aging. 108: 99-109. PMID 34551375 DOI: 10.1016/j.neurobiolaging.2021.08.002 |
0.087 |
|
| 1972 |
Martin L, Trelles L, Martin JJ. [Clinical development of infantile neuro-axonal dystrophy in the light of the chronology of subjacent systematic atrophies]. Journal of the Neurological Sciences. 15: 439-55. PMID 5016692 DOI: 10.1016/0022-510x(72)90170-0 |
0.086 |
|
| 1983 |
Martin JJ, Ceuterick C. Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases. Clinical Neuropathology. 2: 122-7. PMID 6226467 |
0.086 |
|
| 1984 |
Michielsen P, Martin J, Vanagt E, Vrints C, Gillebert T, Snoeck J. Cardiac involvement in juvenile ceroid lipofuscinosis of the Spielmeyer-Vogt-Sjögren type: prospective noninvasive findings in two siblings. European Neurology. 23: 166-172. PMID 6540681 DOI: 10.1159/000115699 |
0.086 |
|
| 1998 |
de Serdio JL, Villar A, Halawa BF, Cejas L, de Miguel B, Martín JJ, López-Aguado D. [Concomitant hyperfractionation of drugs and irradiation in the treatment of advanced ENT cancers]. Anales OtorrinolaringolóGicos Ibero-Americanos. 25: 147-65. PMID 9607225 |
0.086 |
|
| 2014 |
García AM, Mendonça FM, Cejudo MP, Martínez FM, Martín JJ. Superficial Acral Fibromyxoma involving the nail's apparatus. Case report and literature review. Anais Brasileiros De Dermatologia. 89: 147-9. PMID 24626661 DOI: 10.1590/abd1806-4841.20142673 |
0.085 |
|
| 1992 |
Paquier P, van Vugt P, Bal P, Cras P, Parizel PM, van Haesendonck J, Creten W, Martin JJ. Transient musical hallucinosis of central origin: a review and clinical study. Journal of Neurology, Neurosurgery, and Psychiatry. 55: 1069-73. PMID 1469404 DOI: 10.1136/jnnp.55.11.1069 |
0.085 |
|
| 1976 |
Finkelstein JD, Kyle WE, Martin JJ. Abnormal methionine adenosyltransferase in hypermethioninemia. Biochemical and Biophysical Research Communications. 66: 1491-7. PMID 1191305 DOI: 10.1016/0006-291x(75)90527-6 |
0.085 |
|
| 1969 |
Bruens JH, Guazzi GC, Martin JJ. Infantile form of meningeal angiomatosis with sudanophilic leucodystrophy associated with complex abiotrophies. Study of a second family. Journal of the Neurological Sciences. 7: 417-25. PMID 5709854 DOI: 10.1016/0022-510x(68)90050-6 |
0.085 |
|
| 2005 |
Martin JJ. Tumor necrosis factor alpha inhibitors and methotrexate: implications for deployed personnel. Aviation, Space, and Environmental Medicine. 76: 1162-6. PMID 16370267 |
0.085 |
|
| 1973 |
Martin JJ, Schlote W. Neuropathological study of aminoacidurias. Monographs in Human Genetics. 6: 64-78. PMID 4663916 |
0.084 |
|
| 2013 |
Slaets S, Le Bastard N, Martin JJ, Sleegers K, Van Broeckhoven C, De Deyn PP, Engelborghs S. Cerebrospinal fluid Aβ1-40 improves differential dementia diagnosis in patients with intermediate P-tau181P levels. Journal of Alzheimer's Disease : Jad. 36: 759-67. PMID 23666174 DOI: 10.3233/Jad-130107 |
0.084 |
|
| 2012 |
Martin J, Ramesh A, Kamaludeen M, Udhaya, Ganesh K, Martin JJ. Primary Non-Hodgkin's Lymphoma of the Scalp and Cranial Vault. Case Reports in Neurological Medicine. 2012: 616813. PMID 22937355 DOI: 10.1155/2012/616813 |
0.083 |
|
| 1987 |
Martin JJ, Cras P, De Schutter E. Spinal neuroaxonal dystrophy and angioneuromatosis. Acta Neuropathologica. 73: 19-24. PMID 3111160 DOI: 10.1007/BF00695497 |
0.083 |
|
| 1987 |
Landrieu P, Martin JJ. [Movement and cognitive disorders and progressive amyotrophy with onset in early childhood]. Revue Neurologique. 142: 238-46. PMID 3797928 |
0.083 |
|
| 1969 |
de Groodt-Lasseel M, Martin JJ. [Ultrastructural study of central nervous system lesions in Whipple's disease]. Pathologie-Biologie. 17: 121-32. PMID 4182993 |
0.083 |
|
| 2012 |
De Paepe B, Creus KK, Martin JJ, De Bleecker JL. Upregulation of chemokines and their receptors in Duchenne muscular dystrophy: potential for attenuation of myofiber necrosis. Muscle & Nerve. 46: 917-25. PMID 23225384 DOI: 10.1002/mus.23481 |
0.083 |
|
| 1977 |
Martin JJ, Ceuterick C, Martin L, Libert J. Skin and conjunctival biopsies in adrenoleukodystrophy. Acta Neuropathologica. 38: 247-50. PMID 899728 DOI: 10.1007/BF00688074 |
0.083 |
|
| 1996 |
Decaestecker C, Lopes MB, Gordower L, Cras P, Martin JJ, Kiss R, VandenBerg S, Salmon I. CHARACTERIZATION OF THE CHROMATIN PATTERN AND DNA PLOIDY IN OLIGODENDROGLIOMAS, ASTROCYTOMAS, AND MIXED OLIGO-ASTROCYTOMAS Journal of Neuropathology and Experimental Neurology. 55: 654. DOI: 10.1097/00005072-199605000-00205 |
0.082 |
|
| 2019 |
Somers C, Lewczuk P, Sieben A, Van Broeckhoven C, De Deyn PP, Kornhuber J, Martin JJ, Bjerke M, Engelborghs S. Validation of the Erlangen Score Algorithm for Differential Dementia Diagnosis in Autopsy-Confirmed Subjects. Journal of Alzheimer's Disease : Jad. PMID 30883344 DOI: 10.3233/Jad-180563 |
0.082 |
|
| 2015 |
Majersik JJ, Cole JW, Golledge J, Rost NS, Chan YF, Gurol ME, Lindgren AG, Woo D, Fernandez-Cadenas I, Chen DT, Thijs V, Worrall BB, Kamal A, Bentley P, Wardlaw JM, ... ... Martin JJ, et al. Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection. Stroke; a Journal of Cerebral Circulation. 46: 279-84. PMID 25492903 DOI: 10.1161/Strokeaha.114.006839 |
0.082 |
|
| 1982 |
Dubois B, Martin JJ, Develter S, Guérin M, Loeuille GA, Debeugny P, Farriaux JP. [Centronuclear myopathy. Report of a new case]. Annales De Pediatrie. 29: 433-7. PMID 7125507 |
0.081 |
|
| 1966 |
Martin JJ. [Mental disorders in a primary atrophy of the dorso-median thalamic nucleus]. Revue Neurologique. 114: 215-9. PMID 5914978 |
0.081 |
|
| 2016 |
Kadhim H, Deltenre P, Martin JJ, Sébire G. In-situ expression of Interleukin-18 and associated mediators in the human brain of sALS patients: Hypothesis for a role for immune-inflammatory mechanisms. Medical Hypotheses. 86: 14-7. PMID 26804591 DOI: 10.1016/j.mehy.2015.11.022 |
0.08 |
|
| 1999 |
Elleder M, Martin JJ. Mucolipidosis type II with evidence of a novel storage site. Virchows Archiv : An International Journal of Pathology. 433: 575-8. PMID 9870693 DOI: 10.1007/s004280050292 |
0.08 |
|
| 1990 |
Truyen L, Gheuens J, Martin JJ. Patterns of disease activity in multiple sclerosis. Bmj (Clinical Research Ed.). 300: 1272. PMID 2354301 DOI: 10.1136/bmj.300.6734.1272 |
0.08 |
|
| 1969 |
Claes C, Martin JJ. A screening test for neuromuscular disturbances in adynamia episodica hereditaria. Clinical and electrophysiological study. Acta Neurologica Et Psychiatrica Belgica. 68: 460-70. PMID 4304083 |
0.08 |
|
| 1986 |
Appel B, Muller RN, Collard M, Moens E, Mortelmans L, Martin JJ, Lowenthal A. NMR approach of the periventricular white matter. Archives Internationales De Physiologie Et De Biochimie. 93: 19-26. PMID 2424385 DOI: 10.3109/13813458509080621 |
0.079 |
|
| 1968 |
Martin JJ. [The thalamic lesions in Creutzfeldt-Jakob disease and related forms. Topographic study of 13 cases]. Acta Neuropathologica. Suppl 3:92-103. PMID 6074657 |
0.079 |
|
| 1993 |
Nashel DJ, Martin JJ. Images in Rheumatology: a multimedia program for medical education. Proceedings. Symposium On Computer Applications in Medical Care. 798-9. PMID 1482987 |
0.079 |
|
| 1986 |
Dehaene I, Martin JJ, Geens K, Cras P. Guillain-Barré syndrome with ophthalmoplegia: clinicopathologic study of the central and peripheral nervous systems, including the oculomotor nerves. Neurology. 36: 851-4. PMID 3703295 DOI: 10.1212/Wnl.36.6.851 |
0.079 |
|
| 1973 |
Martin JJ, Navarro C, Roussel JM, Michielssen P. Familial capillaro-venous leptomeningeal angiomatosis. European Neurology. 9: 202-15. PMID 4698574 DOI: 10.1159/000114226 |
0.079 |
|
| 1989 |
De Clerck LS, Degryse HR, Wouters E, Van Offel JF, De Schepper AM, Martin JJ, Stevens WJ. Magnetic resonance imaging in the evaluation of patients with eosinophilic fasciitis. The Journal of Rheumatology. 16: 1270-3. PMID 2491737 |
0.079 |
|
| 1993 |
Ceuterick C, Martin JJ. Krabbe globoid cell leukodystrophy. Electron microscopy shows characteristic inclusions in eccrine sweat glands. Pathology, Research and Practice. 189: 384-6. PMID 8394576 DOI: 10.1016/S0344-0338(11)80323-7 |
0.079 |
|
| 2014 |
Engelborghs S, Niemantsverdriet E, Feyen B, Martin J, Goeman J, De Deyn PP. P2-197: VASCULAR DEMENTIA IS OVERDIAGNOSED WHEN STRUCTURAL BRAIN IMAGING IS USED IN THE CONTEXT OF STANDARD CLINICAL DIAGNOSTIC CRITERIA FOR DEMENTIA Alzheimer's & Dementia. 10: P543-P544. DOI: 10.1016/J.Jalz.2014.05.873 |
0.079 |
|
| 2001 |
Marien P, Pickut BA, Engelborghs S, Martin JJ, De Deyn PP. Phonological agraphia following a focal anterior insulo-opercular infarction. Neuropsychologia. 39: 845-55. PMID 11369407 DOI: 10.1016/S0028-3932(01)00006-9 |
0.078 |
|
| 1986 |
Ceuterick C, Martin JJ, Foulard M. Niemann-Pick disease type C. Skin biopsies in parents. Neuropediatrics. 17: 111-2. PMID 3014367 |
0.078 |
|
| 1968 |
Guazzi GC, Martin JJ, Philippart M, Roels H, Hooft C, Van der Eecken H, Delbeke MJ, Vrints L. Wolman's disease. Distribution and significance of the central nervous system lesions. Pathologia Europaea. 3: 266-77. PMID 5688463 |
0.078 |
|
| 2007 |
Mathieu D, Kondziolka D, Flickinger JC, Niranjan A, Williamson R, Martin JJ, Lunsford LD. Stereotactic radiosurgery for vestibular schwannomas in patients with neurofibromatosis type 2: an analysis of tumor control, complications, and hearing preservation rates. Neurosurgery. 60: 460-8; discussion 46. PMID 17327790 DOI: 10.1227/01.Neu.0000255340.26027.53 |
0.078 |
|
| 2015 |
Struyfs H, Niemantsverdriet E, Goossens J, Fransen E, Martin JJ, De Deyn PP, Engelborghs S. Cerebrospinal Fluid P-Tau181P: Biomarker for Improved Differential Dementia Diagnosis. Frontiers in Neurology. 6: 138. PMID 26136723 DOI: 10.3389/Fneur.2015.00138 |
0.078 |
|
| 1975 |
Martin JJ, de Groote C. Involvement of the skin in late infantile and juvenile amaurotic idiocies (neuronal ceroid-lipofuscinoses). Pathologia Europaea. 9: 263-72. PMID 4457780 |
0.077 |
|
| 2015 |
Mata-Cantero L, Cid C, Gomez-Lorenzo MG, Xolalpa W, Aillet F, Martín JJ, Rodriguez MS. Development of two novel high-throughput assays to quantify ubiquitylated proteins in cell lysates: application to screening of new anti-malarials. Malaria Journal. 14: 200. PMID 25968882 DOI: 10.1186/s12936-015-0708-1 |
0.077 |
|
| 1986 |
Martin JJ, Rancurel G, Hauw JJ. [Clinicopathologic conference at the Salpêtrière April 1984. Behavior disorders, convulsive seizures and coma with rapid progression in a 19-year-old man]. Revue Neurologique. 141: 501-6. PMID 4089414 |
0.077 |
|
| 1972 |
Martin JJ, Schlote W. Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study. Journal of the Neurological Sciences. 15: 49-76. PMID 5008716 DOI: 10.1016/0022-510x(72)90121-9 |
0.076 |
|
| 1968 |
Evrard E, Hariga J, Martin JJ, Reznik M. [Late Hallervorden-Spatz disease with important reticular and cerebellar participation]. Psychiatria, Neurologia, Neurochirurgia. 71: 243-54. PMID 5687405 |
0.076 |
|
| 2016 |
Tegazzini D, Díaz R, Aguilar F, Peña I, Presa JL, Yardley V, Martin JJ, Coteron JM, Croft SL, Cantizani J. A Replicative In Vitro Assay for Drug Discovery against Leishmania donovani. Antimicrobial Agents and Chemotherapy. 60: 3524-32. PMID 27021313 DOI: 10.1128/AAC.01781-15 |
0.076 |
|
| 2009 |
Koopman K, Le Bastard N, Martin JJ, Nagels G, De Deyn PP, Engelborghs S. Improved discrimination of autopsy-confirmed Alzheimer's disease (AD) from non-AD dementias using CSF P-tau(181P). Neurochemistry International. 55: 214-8. PMID 19524111 DOI: 10.1016/J.Neuint.2009.02.017 |
0.076 |
|
| 2015 |
Martin JJ. Upper eyelid blepharoplasty with ptosis repair by levator aponeurectomy. Jama Facial Plastic Surgery. 17: 224-5. PMID 25906318 DOI: 10.1001/jamafacial.2015.0198 |
0.075 |
|
| 1965 |
Van Bogaert L, Martin L, Martin JJ. [Amyotrophic lateral sclerosis with spinocerebellar degeneration and epileptic delirium. Contribution to the study of transitional forms of systematized abiotrophies and of the possible relation between the psychic state and certain median thalamic atrophies]. Acta Neurologica Et Psychiatrica Belgica. 65: 845-72. PMID 4956366 |
0.075 |
|
| 2015 |
Debette S, Compter A, Labeyrie MA, Uyttenboogaart M, Metso TM, Majersik JJ, Goeggel-Simonetti B, Engelter ST, Pezzini A, Bijlenga P, Southerland AM, Naggara O, Béjot Y, Cole JW, Ducros A, ... ... Martin JJ, et al. Epidemiology, pathophysiology, diagnosis, and management of intracranial artery dissection. The Lancet. Neurology. 14: 640-654. PMID 25987283 DOI: 10.1016/S1474-4422(15)00009-5 |
0.075 |
|
| 1998 |
Engelborghs S, Mariën P, Martin JJ, De Deyn PP. Functional anatomy, vascularisation and pathology of the human thalamus. Acta Neurologica Belgica. 98: 252-65. PMID 9801706 |
0.075 |
|
| 1992 |
Buntinx IM, Lormans JA, Martin JJ, Dumon JE. A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities. Genetic Counseling (Geneva, Switzerland). 2: 237-40. PMID 1799423 |
0.074 |
|
| 1971 |
Van Bogaert L, Martin JJ. [Critical analysis of the pathology of diffuse cerebro-meningeal angiomatosis without calcification and of Binswanger's encephalopathy]. Journal of the Neurological Sciences. 14: 301-14. PMID 5135337 DOI: 10.1016/0022-510X(71)90219-X |
0.074 |
|
| 2007 |
Le Bastard N, Van Buggenhout M, De Leenheir E, Martin JJ, De Deyn PP, Engelborghs S. LOW specificity limits the use of the cerebrospinal fluid AB1-42/P-TAU181P ratio to discriminate alzheimer's disease from vascular dementia. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 62: 923-4; author reply . PMID 17702886 DOI: 10.1093/Gerona/62.8.923 |
0.074 |
|
| 1998 |
Monsieurs K, Heytens L, Kloeck C, Martin JJ, Wuyts F, Bossaert L. Slower recovery of muscle phosphocreatine in malignant hyperthermia-susceptible individuals assessed by 31P-MR spectroscopy. Journal of Neurology. 244: 651-6. PMID 9402543 DOI: 10.1007/S004150050162 |
0.074 |
|
| 1970 |
Martin JJ, Van Bogaert L, Van Damme J, Peremans J. [Sporadic, generalized pseudo-myopathy in primary endomysial vascular amyloidosis]. Journal of the Neurological Sciences. 11: 147-66. PMID 5456544 DOI: 10.1016/0022-510X(70)90125-5 |
0.074 |
|
| 2011 |
van der Voorn JP, Pouwels PJ, Powers JM, Kamphorst W, Martin JJ, Troost D, Spreeuwenberg MD, Barkhof F, van der Knaap MS. Correlating quantitative MR imaging with histopathology in X-linked adrenoleukodystrophy. Ajnr. American Journal of Neuroradiology. 32: 481-9. PMID 21273354 DOI: 10.3174/Ajnr.A2327 |
0.073 |
|
| 1976 |
Leroy JG, Martin JJ. Mucolipidosis II (I-cell disease): present status of knowledge. Birth Defects Original Article Series. 11: 283-93. PMID 1103995 |
0.073 |
|
| 2012 |
Fendrick AM, Martin JJ, Weiss AE. Value-based insurance design: more health at any price. Health Services Research. 47: 404-13. PMID 22150718 DOI: 10.1111/j.1475-6773.2011.01358.x |
0.072 |
|
| 1981 |
Martin JJ, Ceuterick C, Libert J. Skin and conjunctival nerve biopsies in adrenoleukodystrophy and its variants. Annals of Neurology. 8: 291-5. PMID 7436372 DOI: 10.1002/ana.410080311 |
0.072 |
|
| 2004 |
Hernaez-Ortega MC, Soto-Pedre E, Martin JJ. Sandostatin LAR for cystoid diabetic macular edema: a 1-year experience. Diabetes Research and Clinical Practice. 64: 71-2. PMID 15036829 DOI: 10.1016/j.diabres.2003.10.003 |
0.072 |
|
| 2014 |
Struyfs H, Molinuevo JL, Martin J, De Deyn PP, Engelborghs S. O1-09-05: VALIDATION OF THE AD-CSF INDEX IN AUTOPSY CONFIRMED AD PATIENTS AND HEALTHY CONTROLS Alzheimer's & Dementia. 10: P147-P148. DOI: 10.1016/J.Jalz.2014.04.108 |
0.072 |
|
| 1989 |
Cras P, Franckx C, Martin JJ. Primary intracerebral lymphoma in systemic lupus erythematosus treated with immunosuppressives. Clinical Neuropathology. 8: 200-5. PMID 2673604 |
0.071 |
|
| 1998 |
Gordower L, Decaestecker C, Lopes MB, Camby I, Nagy N, François C, Cras P, Martin JJ, Brotchi J, Kiss R, Salmon I. Determination of growth fraction and cell density to evaluate the potential growth of human oligodendroglial and astrocytic tumours. Journal of Cancer Research and Clinical Oncology. 124: 427-34. PMID 9750019 DOI: 10.1007/s004320050195 |
0.071 |
|
| 1992 |
Heytens L, Martin JJ, Bossaert LL. In vitro diagnosis of malignant hyperthermia: influence of electrical stimulation on the contracture response to caffeine. British Journal of Anaesthesia. 69: 87-91. PMID 1637610 DOI: 10.1093/bja/69.1.87 |
0.071 |
|
| 1984 |
Lowenthal A, Martin JJ. Inflammatory demyelinating disorders in humans. Bulletin De La Societe Belge D'Ophtalmologie. 415-25. PMID 6675827 |
0.071 |
|
| 1978 |
Van Dessel G, Lagrou A, Martin JJ, Dierick W. A case of infantile generalized ceroid-lipofuscinosis. Neurochemical observations [proceedings]. Archives Internationales De Physiologie Et De Biochimie. 85: 1023-5. PMID 79355 DOI: 10.3109/13813457709053343 |
0.071 |
|
| 1967 |
Martin JJ. [Approach to a pathology of the optic layer in abiotrophic, true or presumed metabolic diseases]. Acta Neurologica Et Psychiatrica Belgica. 67: 491-511. PMID 4964209 |
0.07 |
|
| 2008 |
Engelborghs S, Koopman K, Le Bastard N, Martin J, De Deyn PP. P3-068: Improved discrimination of Alzheimer's disease from other dementias using cerebrospinal fluid P-tau181P Alzheimer's & Dementia. 4: T537-T537. DOI: 10.1016/J.Jalz.2008.05.1632 |
0.07 |
|
| 1979 |
Clark E, Moore RC, Martin JJ, Thomasson GO. Pharmaceutical care through a nontraditional outlet Contemporary Pharmacy Practice. 2: 66-72. PMID 10241639 |
0.07 |
|
| 1993 |
De Paepe L, Abs R, Verlooy J, Clemens A, Smets RM, Louis P, Martin JJ. Benign intracranial hypertension as a cause of transient partial pituitary deficiency. Journal of the Neurological Sciences. 114: 152-5. PMID 8445396 |
0.07 |
|
| 2004 |
Ozsarlak O, Parizel PM, De Schepper AM, De Jonghe P, Martin JJ. Whole-body MR screening of muscles in the evaluation of neuromuscular diseases. European Radiology. 14: 1489-93. PMID 15007614 DOI: 10.1007/s00330-004-2270-z |
0.07 |
|
| 1975 |
Martin JJ. Neuropathological study of three cases of primary amoebic meningo-encephalitis. Annales De La Societe Belge De Medecine Tropicale. 54: 305-19. PMID 4429414 |
0.07 |
|
| 2005 |
De Paepe B, De Keyzer K, Martin JJ, De Bleecker JL. Alpha-chemokine receptors CXCR1-3 and their ligands in idiopathic inflammatory myopathies. Acta Neuropathologica. 109: 576-82. PMID 15937690 DOI: 10.1007/s00401-005-0989-5 |
0.069 |
|
| 1991 |
Peetermans JF, Van de Heyning PH, Parizel PM, Martin JJ, Forton GE, Vanmaele RG, Valcke HH, Marquet JF, De Schepper AM. Neurofibroma of the vagus nerve in the head and neck: a case report. Head & Neck. 13: 56-61. PMID 1989931 DOI: 10.1002/hed.2880130109 |
0.069 |
|
| 1993 |
Borggreve F, Dierckx RA, Crols R, Mathijs R, Appel B, Vandevivere J, Mariën P, Martin JJ, De Deyn PP. Repeat thallium-201 SPECT in cerebral lymphoma. Functional Neurology. 8: 95-101. PMID 8330761 |
0.068 |
|
| 1992 |
Mercken M, Vandermeeren M, Lübke U, Six J, Boons J, Van de Voorde A, Martin JJ, Gheuens J. Monoclonal antibodies with selective specificity for Alzheimer Tau are directed against phosphatase-sensitive epitopes. Acta Neuropathologica. 84: 265-72. PMID 1384266 |
0.068 |
|
| 1990 |
Ceuterick C, Martin JJ. Skin biopsy is useful for diagnosis of infantile neuroaxonal dystrophy. Annals of Neurology. 28: 109-10. PMID 2375627 DOI: 10.1002/ana.410280124 |
0.068 |
|
| 2018 |
Norcliffe JL, Mina JG, Alvarez E, Cantizani J, de Dios-Anton F, Colmenarejo G, Valle SG, Marco M, Fiandor JM, Martin JJ, Steel PG, Denny PW. Identifying inhibitors of the Leishmania inositol phosphorylceramide synthase with antiprotozoal activity using a yeast-based assay and ultra-high throughput screening platform. Scientific Reports. 8: 3938. PMID 29500420 DOI: 10.1038/S41598-018-22063-9 |
0.067 |
|
| 1992 |
Martin JJ, Tenzel RR. Acquired ptosis: dehiscences and disinsertions. Are they real or iatrogenic? Ophthalmic Plastic and Reconstructive Surgery. 8: 130-2; discussion 13. PMID 1520655 |
0.067 |
|
| 1984 |
Martin JJ. The visual system in myelin disorders. Histopathological techniques. Bulletin De La Societe Belge D'Ophtalmologie. 41-4. PMID 6675826 |
0.066 |
|
| 1967 |
Martin JJ. [Topography and significance of thalamic lesions in the Creutzfeldt-Jacob disease and its related forms]. Journal Fur Hirnforschung. 8: 137-60. PMID 5982856 |
0.066 |
|
| 2002 |
Van Everbroeck B, Pals P, Martin JJ, Cras P. Transmissible spongiform encephalopathies: the story of a pathogenic protein. Peptides. 23: 1351-9. PMID 12128092 DOI: 10.1016/S0196-9781(02)00071-2 |
0.065 |
|
| 2003 |
Bier JC, Dethy S, Hildebrand J, Jacquy J, Manto M, Martin JJ, Seeldrayers P. Effects of the oral form of ondansetron on cerebellar dysfunction. A multi-center double-blind study. Journal of Neurology. 250: 693-7. PMID 12796831 DOI: 10.1007/s00415-003-1061-9 |
0.064 |
|
| 1974 |
Solheid C, Stoupel N, Martin JJ. [The adult form of Leigh's necrotizing encephalopathy with chronic evolution. Its comparison with the infantile and juvenile forms]. Acta Neurologica Belgica. 71: 282-95. PMID 5005939 |
0.064 |
|
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