| Year |
Citation |
Score |
| 2012 |
van der Beek NA, de Vries JM, Hagemans ML, Hop WC, Kroos MA, Wokke JH, de Visser M, van Engelen BG, Kuks JB, van der Kooi AJ, Notermans NC, Faber KG, Verschuuren JJ, Reuser AJ, van der Ploeg AT, et al. Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study. Orphanet Journal of Rare Diseases. 7: 88. PMID 23147228 DOI: 10.1186/1750-1172-7-88 |
0.309 |
|
| 2012 |
Wadman RI, Bosboom WM, van der Pol WL, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. 4: CD006282. PMID 22513940 DOI: 10.1002/14651858.Cd006282.Pub4 |
0.462 |
|
| 2012 |
Wadman RI, Bosboom WM, van der Pol WL, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. 4: CD006281. PMID 22513939 DOI: 10.1002/14651858.Cd006281.Pub4 |
0.467 |
|
| 2012 |
De Visser M, van der Kooi A, Linssen WHJP, Ginjaar I, Wokke J, Van Doorn P. Anoctamin 5 Mutations Are a Frequent Cause of Limb Girdle Muscular Dystrophy and of the Miyoshi-Type Muscular Dystrophy in the Netherlands (S15.005) Neurology. 78: S15.005-S15.005. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S15.005 |
0.342 |
|
| 2011 |
Wadman RI, Bosboom WM, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. CD006282. PMID 22161400 DOI: 10.1002/14651858.CD006282.pub3 |
0.389 |
|
| 2011 |
Wadman RI, Bosboom WM, van den Berg LH, Wokke JH, Iannaccone ST, Vrancken AF. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. CD006281. PMID 22161399 DOI: 10.1002/14651858.CD006281.pub3 |
0.394 |
|
| 2011 |
Visser NA, Braun KP, Leijten FS, van Nieuwenhuizen O, Wokke JH, van den Bergh WM. Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations. Journal of Neurology. 258: 218-22. PMID 20803213 DOI: 10.1007/S00415-010-5721-2 |
0.316 |
|
| 2011 |
Straver DC, van Asseldonk JT, Notermans NC, Wokke JH, van den Berg LH, Franssen H. Cold paresis in multifocal motor neuropathy. Journal of Neurology. 258: 212-7. PMID 20803025 DOI: 10.1007/S00415-010-5712-3 |
0.524 |
|
| 2011 |
Piepers S, Cobben JM, Sodaar P, Jansen MD, Wadman RI, Meester-Delver A, Poll-The BT, Lemmink HH, Wokke JH, van der Pol WL, van den Berg LH. Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 850-2. PMID 20551479 DOI: 10.1136/Jnnp.2009.200253 |
0.472 |
|
| 2010 |
Franssen H, Gebbink TA, Wokke JH, van den Berg LH, van Schelven LJ. Is cold paresis related to axonal depolarization? Journal of the Peripheral Nervous System : Jpns. 15: 227-37. PMID 21040145 DOI: 10.1111/J.1529-8027.2010.00275.X |
0.503 |
|
| 2010 |
Niks EH, Kuks JB, Wokke JH, Veldman H, Bakker E, Verschuuren JJ, Plomp JJ. Pre- and postsynaptic neuromuscular junction abnormalities in musk myasthenia. Muscle & Nerve. 42: 283-8. PMID 20544919 DOI: 10.1002/Mus.21642 |
0.337 |
|
| 2010 |
Groen EJ, van Es MA, van Vught PW, Spliet WG, van Engelen-Lee J, de Visser M, Wokke JH, Schelhaas HJ, Ophoff RA, Fumoto K, Pasterkamp RJ, Dooijes D, Cuppen E, Veldink JH, van den Berg LH. FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands. Archives of Neurology. 67: 224-30. PMID 20142531 DOI: 10.1001/Archneurol.2009.329 |
0.436 |
|
| 2009 |
Van Es MA, Van Vught PW, Veldink JH, Andersen PM, Birve A, Lemmens R, Cronin S, Van Der Kooi AJ, De Visser M, Schelhaas HJ, Hardiman O, Ragoussis I, Lambrechts D, Robberecht W, Wokke JH, et al. Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 10: 441-7. PMID 19922138 DOI: 10.3109/17482960802673042 |
0.443 |
|
| 2009 |
Sutedja NA, Veldink JH, Fischer K, Kromhout H, Heederik D, Huisman MH, Wokke JH, van den Berg LH. Exposure to chemicals and metals and risk of amyotrophic lateral sclerosis: a systematic review. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 10: 302-9. PMID 19922117 DOI: 10.3109/17482960802455416 |
0.42 |
|
| 2009 |
Maessen M, Veldink JH, Onwuteaka-Philipsen BD, de Vries JM, Wokke JH, van der Wal G, van den Berg LH. Trends and determinants of end-of-life practices in ALS in the Netherlands. Neurology. 73: 954-61. PMID 19770471 DOI: 10.1212/WNL.0b013e3181b87983 |
0.367 |
|
| 2009 |
Piepers S, Veldink JH, de Jong SW, van der Tweel I, van der Pol WL, Uijtendaal EV, Schelhaas HJ, Scheffer H, de Visser M, de Jong JM, Wokke JH, Groeneveld GJ, van den Berg LH. Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis. Annals of Neurology. 66: 227-34. PMID 19743466 DOI: 10.1002/Ana.21620 |
0.427 |
|
| 2009 |
van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, ... ... Wokke JH, et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nature Genetics. 41: 1083-7. PMID 19734901 DOI: 10.1038/Ng.442 |
0.414 |
|
| 2009 |
Saris CG, Horvath S, van Vught PW, van Es MA, Blauw HM, Fuller TF, Langfelder P, DeYoung J, Wokke JH, Veldink JH, van den Berg LH, Ophoff RA. Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. Bmc Genomics. 10: 405. PMID 19712483 DOI: 10.1186/1471-2164-10-405 |
0.5 |
|
| 2009 |
Faber CG, Molenaar PC, Vles JS, Bonifati DM, Verschuuren JJ, van Doorn PA, Kuks JB, Wokke JH, Beeson D, De Baets M. AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands. Journal of Neurology. 256: 1719-23. PMID 19544078 DOI: 10.1007/S00415-009-5190-7 |
0.301 |
|
| 2009 |
Piepers S, van der Pol WL, Brugman F, Wokke JH, van den Berg LH. Natural history of SMA IIIb: muscle strength decreases in a predictable sequence and magnitude. Neurology. 72: 2057-8; author reply. PMID 19506238 DOI: 10.1212/01.wnl.0000349698.94744.1e |
0.362 |
|
| 2009 |
Van den Berg-Vos RM, Visser J, Kalmijn S, Fischer K, de Visser M, de Jong V, de Haan RJ, Franssen H, Wokke JH, Van den Berg LH. A long-term prospective study of the natural course of sporadic adult-onset lower motor neuron syndromes. Archives of Neurology. 66: 751-7. PMID 19506135 DOI: 10.1001/Archneurol.2009.91 |
0.483 |
|
| 2009 |
Landers JE, Melki J, Meininger V, Glass JD, van den Berg LH, van Es MA, Sapp PC, van Vught PW, McKenna-Yasek DM, Blauw HM, Cho TJ, Polak M, Shi L, Wills AM, Broom WJ, ... ... Wokke JH, et al. Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 106: 9004-9. PMID 19451621 DOI: 10.1073/Pnas.0812937106 |
0.467 |
|
| 2009 |
Brugman F, Veldink JH, Franssen H, de Visser M, de Jong JM, Faber CG, Kremer BH, Schelhaas HJ, van Doorn PA, Verschuuren JJ, Bruyn RP, Kuks JB, Robberecht W, Wokke JH, van den Berg LH. Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes. Archives of Neurology. 66: 509-14. PMID 19364936 DOI: 10.1001/Archneurol.2009.19 |
0.529 |
|
| 2009 |
Faber CG, Notermans NC, Wokke JH, Franssen H. Entrapment in anti myelin-associated glycoprotein neuropathy. Journal of Neurology. 256: 620-4. PMID 19306083 DOI: 10.1007/S00415-009-0132-Y |
0.365 |
|
| 2009 |
Brugman F, Scheffer H, Schelhaas HJ, Nillesen WM, Wokke JH, van de Warrenburg BP, van den Berg LH. Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. Journal of Neurology. 256: 824-6. PMID 19252810 DOI: 10.1007/S00415-009-5009-6 |
0.51 |
|
| 2009 |
Bosboom W, Vrancken AF, van den Berg LH, Wokke JH, Iannaccone ST. Drug treatment for spinal muscular atrophy types II and III. The Cochrane Database of Systematic Reviews. CD006282. PMID 19160275 DOI: 10.1002/14651858.CD006282.pub2 |
0.388 |
|
| 2009 |
Bosboom W, Vrancken AF, van den Berg LH, Wokke J, Iannaccone ST. Drug treatment for spinal muscular atrophy type I. The Cochrane Database of Systematic Reviews. CD006281. PMID 19160274 DOI: 10.1002/14651858.CD006281.pub2 |
0.407 |
|
| 2008 |
Wokke JH, Escolar DM, Pestronk A, Jaffe KM, Carter GT, van den Berg LH, Florence JM, Mayhew J, Skrinar A, Corzo D, Laforet P. Clinical features of late-onset Pompe disease: a prospective cohort study. Muscle & Nerve. 38: 1236-45. PMID 18816591 DOI: 10.1002/Mus.21025 |
0.492 |
|
| 2008 |
Brugman F, Scheffer H, Wokke JH, Nillesen WM, de Visser M, Aronica E, Veldink JH, van den Berg LH. Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes. Neurology. 71: 1500-5. PMID 18799786 DOI: 10.1212/01.wnl.0000319700.11606.21 |
0.41 |
|
| 2008 |
Piepers S, van den Berg LH, Brugman F, Scheffer H, Ruiterkamp-Versteeg M, van Engelen BG, Faber CG, de Visser M, van der Pol WL, Wokke JH. A natural history study of late onset spinal muscular atrophy types 3b and 4. Journal of Neurology. 255: 1400-4. PMID 18575920 DOI: 10.1007/S00415-008-0929-0 |
0.323 |
|
| 2008 |
Dierick I, Baets J, Irobi J, Jacobs A, De Vriendt E, Deconinck T, Merlini L, Van den Bergh P, Rasic VM, Robberecht W, Fischer D, Morales RJ, Mitrovic Z, Seeman P, Mazanec R, ... ... Wokke JH, et al. Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study. Brain : a Journal of Neurology. 131: 1217-27. PMID 18325928 DOI: 10.1093/Brain/Awn029 |
0.329 |
|
| 2008 |
Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, Franke L, Burbach JP, Wokke JH, Ophoff RA, van den Berg LH. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen. The Lancet. Neurology. 7: 319-26. PMID 18313986 DOI: 10.1016/S1474-4422(08)70048-6 |
0.403 |
|
| 2008 |
van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, Van den Bosch L, de Jong SW, de Jong V, Baas F, van't Slot R, Lemmens R, Schelhaas HJ, Birve A, Sleegers K, Van Broeckhoven C, ... ... Wokke JH, et al. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nature Genetics. 40: 29-31. PMID 18084291 DOI: 10.1038/Ng.2007.52 |
0.454 |
|
| 2007 |
Van Den Berg LH, Franssen H, Van Asseldonk JT, Van Den Berg-Vos RM, Wokke JH. Chapter 12 Multifocal and other motor neuropathies. Handbook of Clinical Neurology. 82: 229-45. PMID 18808897 DOI: 10.1016/S0072-9752(07)80015-7 |
0.507 |
|
| 2007 |
Sutedja NA, Veldink JH, Fischer K, Kromhout H, Wokke JH, Huisman MH, Heederik DJ, Van den Berg LH. Lifetime occupation, education, smoking, and risk of ALS. Neurology. 69: 1508-14. PMID 17923612 DOI: 10.1212/01.wnl.0000277463.87361.8c |
0.324 |
|
| 2007 |
van Es MA, Van Vught PW, Blauw HM, Franke L, Saris CG, Andersen PM, Van Den Bosch L, de Jong SW, van 't Slot R, Birve A, Lemmens R, de Jong V, Baas F, Schelhaas HJ, Sleegers K, ... ... Wokke JH, et al. ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. The Lancet. Neurology. 6: 869-77. PMID 17827064 DOI: 10.1016/S1474-4422(07)70222-3 |
0.481 |
|
| 2007 |
Brugman F, Eymard-Pierre E, van den Berg LH, Wokke JH, Gauthier-Barichard F, Boespflug-Tanguy O. Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene. Neurology. 69: 702-4. PMID 17698795 DOI: 10.1212/01.wnl.0000267322.48364.76 |
0.363 |
|
| 2007 |
Piepers S, Van Den Berg-Vos R, Van Der Pol WL, Franssen H, Wokke J, Van Den Berg L. Mycophenolate mofetil as adjunctive therapy for MMN patients: A randomized, controlled trial Brain. 130: 2004-2010. PMID 17626040 DOI: 10.1093/Brain/Awm144 |
0.521 |
|
| 2007 |
Niermeijer JM, Eurelings M, van der Linden MW, Lokhorst HM, Franssen H, Fischer K, Teunissen LL, van den Berg LH, Schobben F, Wokke JH, Notermans NC. Intermittent cyclophosphamide with prednisone versus placebo for polyneuropathy with IgM monoclonal gammopathy. Neurology. 69: 50-9. PMID 17606880 DOI: 10.1212/01.wnl.0000265055.28218.cc |
0.37 |
|
| 2007 |
Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Wokke JH, de Jong JM, Holman R, de Haan RJ, de Visser M. Disease course and prognostic factors of progressive muscular atrophy. Archives of Neurology. 64: 522-8. PMID 17420313 DOI: 10.1001/archneur.64.4.522 |
0.437 |
|
| 2007 |
Wokke JH. Fatigue is part of the burden of neuromuscular diseases. Journal of Neurology. 254: 948-9. PMID 17325819 DOI: 10.1007/S00415-006-0436-0 |
0.348 |
|
| 2007 |
Sutedja NA, Sinke RJ, Van Vught PW, Van der Linden MW, Wokke JH, Van Duijn CM, Njajou OT, Van der Schouw YT, Veldink JH, Van den Berg LH. The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population. Archives of Neurology. 64: 63-7. PMID 17210810 DOI: 10.1001/Archneur.64.1.63 |
0.445 |
|
| 2007 |
van Sorge NM, Yuki N, Jansen MD, Nishimoto Y, Susuki K, Wokke JH, van de Winkel JG, van den Berg LH, van der Pol WL. Leukocyte and complement activation by GM1-specific antibodies is associated with acute motor axonal neuropathy in rabbits. Journal of Neuroimmunology. 182: 116-23. PMID 17161468 DOI: 10.1016/J.Jneuroim.2006.10.005 |
0.669 |
|
| 2007 |
van Sorge NM, Yuki N, Koga M, Susuki K, Jansen MD, van Kooten C, Wokke JH, van de Winkel JG, van der Pol WL, van den Berg LH. Ganglioside-specific IgG and IgA recruit leukocyte effector functions in Guillain-Barré syndrome. Journal of Neuroimmunology. 182: 177-84. PMID 17156858 DOI: 10.1016/J.Jneuroim.2006.10.015 |
0.662 |
|
| 2007 |
Veldink JH, Kalmijn S, Groeneveld GJ, Wunderink W, Koster A, de Vries JH, van der Luyt J, Wokke JH, Van den Berg LH. Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 367-71. PMID 16648143 DOI: 10.1136/jnnp.2005.083378 |
0.335 |
|
| 2006 |
Piepers S, van den Berg JP, Kalmijn S, van der Pol WL, Wokke JH, Lindeman E, van den Berg LH. Effect of non-invasive ventilation on survival, quality of life, respiratory function and cognition: a review of the literature. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 7: 195-200. PMID 17127557 DOI: 10.1080/14660820500514974 |
0.453 |
|
| 2006 |
Van Asseldonk JT, Van den Berg LH, Wieneke GH, Wokke JH, Franssen H. Criteria for conduction block based on computer simulation studies of nerve conduction with human data obtained in the forearm segment of the median nerve. Brain : a Journal of Neurology. 129: 2447-60. PMID 16923956 DOI: 10.1093/brain/awl197 |
0.416 |
|
| 2006 |
Van Asseldonk JT, Van den Berg LH, Kalmijn S, Van den Berg-Vos RM, Polman CH, Wokke JH, Franssen H. Axon loss is an important determinant of weakness in multifocal motor neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 77: 743-7. PMID 16705197 DOI: 10.1136/jnnp.2005.064816 |
0.443 |
|
| 2005 |
Van Vught PW, Sutedja NA, Veldink JH, Koeleman BP, Groeneveld GJ, Wijmenga C, Uitdehaag BM, de Jong JM, Baas F, Wokke JH, Van den Berg LH. Lack of association between VEGF polymorphisms and ALS in a Dutch population. Neurology. 65: 1643-5. PMID 16301496 DOI: 10.1212/01.Wnl.0000184514.39853.56 |
0.362 |
|
| 2005 |
Wokke JH, van den Berg LH. A way out of the maze: Campylobacter jejuni gene polymorphisms define Guillain-Barré syndrome. Neurology. 65: 1350-1. PMID 16275819 DOI: 10.1212/01.Wnl.0000185127.89668.7A |
0.506 |
|
| 2005 |
Van den Berg JP, Kalmijn S, Lindeman E, Veldink JH, de Visser M, Van der Graaff MM, Wokke JH, Van den Berg LH. Multidisciplinary ALS care improves quality of life in patients with ALS. Neurology. 65: 1264-7. PMID 16247055 DOI: 10.1212/01.wnl.0000180717.29273.12 |
0.362 |
|
| 2005 |
Brugman F, Wokke JH, Scheffer H, Versteeg MH, Sistermans EA, van den Berg LH. Spastin mutations in sporadic adult-onset upper motor neuron syndromes. Annals of Neurology. 58: 865-9. PMID 16240363 DOI: 10.1002/Ana.20652 |
0.509 |
|
| 2005 |
Losen M, Stassen MH, MartÃnez-MartÃnez P, Machiels BM, Duimel H, Frederik P, Veldman H, Wokke JH, Spaans F, Vincent A, De Baets MH. Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis. Brain : a Journal of Neurology. 128: 2327-37. PMID 16150851 DOI: 10.1093/Brain/Awh612 |
0.313 |
|
| 2005 |
Veldink JH, Kalmijn S, Van der Hout AH, Lemmink HH, Groeneveld GJ, Lummen C, Scheffer H, Wokke JH, Van den Berg LH. SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS. Neurology. 65: 820-5. PMID 16093455 DOI: 10.1212/01.wnl.0000174472.03292.dd |
0.411 |
|
| 2005 |
Beekman R, van den Berg LH, Franssen H, Visser LH, van Asseldonk JT, Wokke JH. Ultrasonography shows extensive nerve enlargements in multifocal motor neuropathy. Neurology. 65: 305-7. PMID 16043806 DOI: 10.1212/01.wnl.0000169179.67764.30 |
0.423 |
|
| 2005 |
Erdmann PG, van Meeteren NL, Kalmijn S, Wokke JH, Helders PJ, van den Berg LH. Functional health status of patients with chronic inflammatory neuropathies. Journal of the Peripheral Nervous System : Jpns. 10: 181-9. PMID 15958129 DOI: 10.1111/J.1085-9489.2005.0010208.X |
0.481 |
|
| 2005 |
Brugman F, Wokke JH, Vianney de Jong JM, Franssen H, Faber CG, Van den Berg LH. Primary lateral sclerosis as a phenotypic manifestation of familial ALS. Neurology. 64: 1778-9. PMID 15911810 DOI: 10.1212/01.WNL.0000162033.47893.F7 |
0.394 |
|
| 2005 |
Van Asseldonk JT, Franssen H, Van den Berg-Vos RM, Wokke JH, Van den Berg LH. Multifocal motor neuropathy. The Lancet. Neurology. 4: 309-19. PMID 15847844 DOI: 10.1016/S1474-4422(05)70074-0 |
0.551 |
|
| 2005 |
van Sorge NM, van der Pol WL, Jansen MD, Geleijns KP, Kalmijn S, Hughes RA, Rees JH, Pritchard J, Vedeler CA, Myhr KM, Shaw C, van Schaik IN, Wokke JH, van Doorn PA, Jacobs BC, et al. Severity of Guillain-Barré syndrome is associated with Fc gamma Receptor III polymorphisms. Journal of Neuroimmunology. 162: 157-64. PMID 15833371 DOI: 10.1016/J.Jneuroim.2005.01.016 |
0.67 |
|
| 2005 |
Groeneveld GJ, Beijer C, Veldink JH, Kalmijn S, Wokke JH, van den Berg LH. Few adverse effects of long-term creatine supplementation in a placebo-controlled trial. International Journal of Sports Medicine. 26: 307-13. PMID 15795816 DOI: 10.1055/s-2004-817917 |
0.376 |
|
| 2005 |
Van Asseldonk JT, Van den Berg LH, Kalmijn S, Wokke JH, Franssen H. Criteria for demyelination based on the maximum slowing due to axonal degeneration, determined after warming in water at 37 degrees C: diagnostic yield in chronic inflammatory demyelinating polyneuropathy. Brain : a Journal of Neurology. 128: 880-91. PMID 15689367 DOI: 10.1093/brain/awh375 |
0.444 |
|
| 2005 |
Veldink JH, Kalmijn S, Groeneveld GJ, Titulaer MJ, Wokke JH, van den Berg LH. Physical activity and the association with sporadic ALS. Neurology. 64: 241-5. PMID 15668420 DOI: 10.1212/01.WNL.0000149513.82332.5C |
0.36 |
|
| 2004 |
Groeneveld GJ, van Muiswinkel FL, de Leeuw van Weenen J, Blauw H, Veldink JH, Wokke JH, van den Berg LH, Bär PR. CGP 3466B has no effect on disease course of (G93A) mSOD1 transgenic mice. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 5: 220-5. PMID 15799550 DOI: 10.1080/14660820410019530 |
0.423 |
|
| 2004 |
Groeneveld GJ, van der Tweel I, Wokke JH, van den Berg LH. Sequential designs for clinical trials in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 5: 202-7. PMID 15799547 |
0.339 |
|
| 2004 |
Veldink JH, Van den Berg LH, Wokke JH. The future of motor neuron disease: the challenge is in the genes. Journal of Neurology. 251: 491-500. PMID 15083302 DOI: 10.1007/S00415-004-0322-6 |
0.501 |
|
| 2004 |
Vrancken AF, Notermans NC, Jansen GH, Wokke JH, Said G. Progressive idiopathic axonal neuropathy--a comparative clinical and histopathological study with vasculitic neuropathy. Journal of Neurology. 251: 269-78. PMID 15015005 DOI: 10.1007/S00415-004-0275-9 |
0.355 |
|
| 2004 |
Beekman R, Schoemaker MC, Van Der Plas JP, Van Den Berg LH, Franssen H, Wokke JH, Uitdehaag BM, Visser LH. Diagnostic value of high-resolution sonography in ulnar neuropathy at the elbow. Neurology. 62: 767-73. PMID 15007128 DOI: 10.1212/01.WNL.0000113733.62689.0D |
0.331 |
|
| 2004 |
Groeneveld GJ, Van Kan HJ, Kalmijn S, Veldink JH, Guchelaar HJ, Wokke JH, Van den Berg LH. Riluzole serum concentrations in patients with ALS: associations with side effects and symptoms. Neurology. 61: 1141-3. PMID 14581684 DOI: 10.1212/01.WNL.0000090459.76784.49 |
0.408 |
|
| 2004 |
Eurelings M, van den Berg LH, Wokke JH, Franssen H, Vrancken AF, Notermans NC. Increase of sural nerve T cells in progressive axonal polyneuropathy and monoclonal gammopathy. Neurology. 61: 707-9. PMID 12963771 DOI: 10.1212/01.WNL.0000078103.71192.40 |
0.441 |
|
| 2003 |
Van Den Berg-Vos RM, Van Den Berg LH, Visser J, de Visser M, Franssen H, Wokke JH. The spectrum of lower motor neuron syndromes. Journal of Neurology. 250: 1279-92. PMID 14648143 DOI: 10.1007/S00415-003-0235-9 |
0.368 |
|
| 2003 |
Visser J, Mans E, de Visser M, van den Berg-Vos RM, Franssen H, de Jong JM, van den Berg LH, Wokke JH, de Haan RJ. Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndrome. Neuromuscular Disorders : Nmd. 13: 744-50. PMID 14561498 DOI: 10.1016/S0960-8966(03)00135-4 |
0.359 |
|
| 2003 |
Reagan P, Hurst R, Cook L, Zylicz Z, Otlowski M, Veldink JH, van den Berg LH, Wokke JH. Physician-assisted death: dying with dignity? The Lancet. Neurology. 2: 637-43. PMID 14505588 DOI: 10.1016/S1474-4422(03)00536-2 |
0.463 |
|
| 2003 |
van den Berg JP, Kalmijn S, Lindeman E, Wokke JH, van den Berg LH. Rehabilitation care for patients with ALS in The Netherlands. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 4: 186-90. PMID 13129805 DOI: 10.1080/Aml.4.3.186.190 |
0.468 |
|
| 2003 |
Teunissen LL, Notermans NC, Franssen H, Van Engelen BG, Baas F, Wokke JH. Disease course of Charcot-Marie-Tooth disease type 2: a 5-year follow-up study. Archives of Neurology. 60: 823-8. PMID 12810486 DOI: 10.1001/Archneur.60.6.823 |
0.323 |
|
| 2003 |
van Sorge NM, van den Berg LH, Geleijns K, van Strijp JA, Jacobs BC, van Doorn PA, Wokke JH, van de Winkel JG, Leusen JH, van der Pol WL. Anti-GM1 IgG antibodies induce leukocyte effector functions via Fcgamma receptors. Annals of Neurology. 53: 570-9. PMID 12730990 DOI: 10.1002/Ana.10503 |
0.652 |
|
| 2003 |
van den Berg-Vos RM, Visser J, Franssen H, de Visser M, de Jong JM, Kalmijn S, Wokke JH, van den Berg LH. Sporadic lower motor neuron disease with adult onset: classification of subtypes. Brain : a Journal of Neurology. 126: 1036-47. PMID 12690044 DOI: 10.1093/Brain/Awg117 |
0.527 |
|
| 2003 |
Groeneveld GJ, Veldink JH, van der Tweel I, Kalmijn S, Beijer C, de Visser M, Wokke JH, Franssen H, van den Berg LH. A randomized sequential trial of creatine in amyotrophic lateral sclerosis. Annals of Neurology. 53: 437-45. PMID 12666111 DOI: 10.1002/Ana.10554 |
0.488 |
|
| 2003 |
Van Asseldonk JT, Van den Berg LH, Van den Berg-Vos RM, Wieneke GH, Wokke JH, Franssen H. Demyelination and axonal loss in multifocal motor neuropathy: distribution and relation to weakness. Brain : a Journal of Neurology. 126: 186-98. PMID 12477706 DOI: 10.1093/Brain/Awg019 |
0.518 |
|
| 2003 |
van der Meulen MF, van Wichen DF, van Blokland WT, van den Berg LH, Wokke JH, Hoogendijk JE, de Weger RA. Evidence for heterogeneity of T cell expansion in polymyositis and inclusion body myositis. Journal of Neuroimmunology. 133: 198-204. PMID 12446023 DOI: 10.1016/S0165-5728(02)00363-6 |
0.508 |
|
| 2002 |
Van den Berg-Vos RM, Franssen H, Wokke JH, Van den Berg LH. Multifocal motor neuropathy: long-term clinical and electrophysiological assessment of intravenous immunoglobulin maintenance treatment. Brain : a Journal of Neurology. 125: 1875-86. PMID 12135977 DOI: 10.1093/Brain/Awf193 |
0.533 |
|
| 2002 |
Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Vogels OJ, Wokke JH, de Jong JM, de Visser M. Mimic syndromes in sporadic cases of progressive spinal muscular atrophy. Neurology. 58: 1593-6. PMID 12058084 DOI: 10.1212/Wnl.58.11.1593 |
0.55 |
|
| 2002 |
Veldink JH, Wokke JH, van der Wal G, Vianney de Jong JM, van den Berg LH. Euthanasia and physician-assisted suicide among patients with amyotrophic lateral sclerosis in the Netherlands. The New England Journal of Medicine. 346: 1638-44. PMID 12023997 DOI: 10.1056/Nejmsa012739 |
0.474 |
|
| 2002 |
Van den Berg-Vos RM, Franssen H, Visser J, de Visser M, de Haan RJ, Wokke JH, Van den Berg LH. Disease severity in multifocal motor neuropathy and its association with the response to immunoglobulin treatment. Journal of Neurology. 249: 330-6. PMID 11993534 DOI: 10.1046/J.1529-8027.2002.02032_4.X |
0.534 |
|
| 2002 |
Oey PL, Vos PE, Wieneke GH, Wokke JH, Blankestijn PJ, Karemaker JM. Subtle involvement of the sympathetic nervous system in amyotrophic lateral sclerosis. Muscle & Nerve. 25: 402-8. PMID 11870718 DOI: 10.1002/Mus.10049 |
0.331 |
|
| 2002 |
Bosboom WM, van den Berg LH, Franssen H, Giesbergen PC, Flach HZ, van Putten AM, Veldman H, Wokke JH. Diagnostic value of sural nerve demyelination in chronic inflammatory demyelinating polyneuropathy. Brain : a Journal of Neurology. 124: 2427-38. PMID 11701597 DOI: 10.1093/BRAIN/124.12.2427 |
0.436 |
|
| 2001 |
Eurelings M, Notermans NC, Franssen H, Van Es HW, Ramos LM, Wokke JH, van den Berg LH. MRI of the brachial plexus in polyneuropathy associated with monoclonal gammopathy. Muscle & Nerve. 24: 1312-8. PMID 11562910 DOI: 10.1002/Mus.1149 |
0.507 |
|
| 2001 |
van der Meulen MF, Hoogendijk JE, Moons KG, Veldman H, Badrising UA, Wokke JH. Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositis. Neuromuscular Disorders : Nmd. 11: 447-51. PMID 11404115 DOI: 10.1016/S0960-8966(00)00219-4 |
0.329 |
|
| 2001 |
Van den Berg-Vos RM, Van den Berg LH, Jansen GH, Parton M, Shaw CE, Hesseling-Janssen AL, Wokke JH. Hereditary pure lower motor neuron disease with adult onset and rapid progression. Journal of Neurology. 248: 290-6. PMID 11374093 DOI: 10.1007/S004150170203 |
0.504 |
|
| 2001 |
Veldink JH, van den Berg LH, Cobben JM, Stulp RP, De Jong JM, Vogels OJ, Baas F, Wokke JH, Scheffer H. Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 56: 749-52. PMID 11274309 |
0.422 |
|
| 2001 |
Eurelings M, Moons KG, Notermans NC, Sasker LD, De Jager AE, Wintzen AR, Wokke JH, Van den Berg LH. Neuropathy and IgM M-proteins: prognostic value of antibodies to MAG, SGPG, and sulfatide. Neurology. 56: 228-33. PMID 11160960 DOI: 10.1212/WNL.56.2.228 |
0.397 |
|
| 2001 |
Bosboom WM, Van den Berg LH, Mollee I, Sasker LD, Jansen J, Wokke JH, Logtenberg T. Sural nerve T-cell receptor Vbeta gene utilization in chronic inflammatory demyelinating polyneuropathy and vasculitic neuropathy. Neurology. 56: 74-81. PMID 11148239 DOI: 10.1212/WNL.56.1.74 |
0.661 |
|
| 2001 |
Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, et al. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy. Journal of Neurology. 247: 524-9. PMID 10993494 DOI: 10.1007/S004150070151 |
0.308 |
|
| 2001 |
Teunissen LL, Notermans NC, Jansen GH, Banga JD, Veldman H, Wokke JH. Thickness of endoneurial vessel basal lamina area in chronic idiopathic axonal polyneuropathy. Acta Neuropathologica. 100: 445-50. PMID 10985705 DOI: 10.1007/S004010000193 |
0.321 |
|
| 2000 |
Weijnen FG, van der Bilt A, Wokke JH, Kuks JB, van der Glas HW, Bosman F. Maximal bite force and surface EMG in patients with myasthenia gravis. Muscle & Nerve. 23: 1694-9. PMID 11054747 DOI: 10.1002/1097-4598(200011)23:11<1694::Aid-Mus4>3.0.Co;2-H |
0.346 |
|
| 2000 |
van der Kooi AJ, Visser MC, Rosenberg N, van den Berg-Vos R, Wokke JH, Bakker E, de Visser M. Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 114-6. PMID 10864616 DOI: 10.1136/Jnnp.69.1.114 |
0.328 |
|
| 2000 |
van der Pol WL, van den Berg LH, Scheepers RH, van der Bom JG, van Doorn PA, van Koningsveld R, van den Broek MC, Wokke JH, van de Winkel JG. IgG receptor IIa alleles determine susceptibility and severity of Guillain-Barré syndrome. Neurology. 54: 1661-5. PMID 10762510 DOI: 10.1212/WNL.54.8.1661 |
0.414 |
|
| 2000 |
Reijneveld JC, Notermans NC, Linssen WH, Wokke JH. Benign prognosis in idiopathic hyper-CK-emia. Muscle & Nerve. 23: 575-9. PMID 10716769 DOI: 10.1002/(Sici)1097-4598(200004)23:4<575::Aid-Mus17>3.0.Co;2-5 |
0.371 |
|
| 2000 |
Weijnen FG, van der Bilt A, Wokke JH, Kuks JB, van der Glas HW, Bosman F. What's in a smile?: Quantification of the vertical smile of patients with myasthenia gravis. Journal of the Neurological Sciences. 173: 124-8. PMID 10675656 DOI: 10.1016/S0022-510X(99)00319-6 |
0.355 |
|
| 2000 |
Van den Berg-Vos RM, Van den Berg LH, Franssen H, Vermeulen M, Witkamp TD, Jansen GH, van Es HW, Kerkhoff H, Wokke JH. Multifocal inflammatory demyelinating neuropathy: a distinct clinical entity? Neurology. 54: 26-32. PMID 10636121 DOI: 10.1212/WNL.54.1.26 |
0.453 |
|
| 1999 |
Bosboom WM, Van den Berg LH, De Boer L, Van Son MJ, Veldman H, Franssen H, Logtenberg T, Wokke JH. The diagnostic value of sural nerve T cells in chronic inflammatory demyelinating polyneuropathy. Neurology. 53: 837-45. PMID 10489051 DOI: 10.1212/WNL.53.4.837 |
0.656 |
|
| 1999 |
Wokke JH, Van den Berg LH. New hope for patients with pure lower motor neuron syndromes. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 6. PMID 10369813 DOI: 10.1136/JNNP.67.1.6 |
0.42 |
|
| 1998 |
Van den Berg LH, Franssen H, Wokke JH. The long-term effect of intravenous immunoglobulin treatment in multifocal motor neuropathy. Brain : a Journal of Neurology. 421-8. PMID 9549518 DOI: 10.1093/BRAIN/121.3.421 |
0.457 |
|
| 1998 |
van den Berg LH, Franssen H, Van Doorn PA, Wokke JH. Intravenous immunoglobulin treatment in lower motor neuron disease associated with highly raised anti-GM1 antibodies. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 674-7. PMID 9408114 DOI: 10.1136/jnnp.63.5.674 |
0.453 |
|
| 1997 |
Van Es HW, Van den Berg LH, Franssen H, Witkamp TD, Ramos LM, Notermans NC, Feldberg MA, Wokke JH. Magnetic resonance imaging of the brachial plexus in patients with multifocal motor neuropathy. Neurology. 48: 1218-24. PMID 9153446 DOI: 10.1212/WNL.48.5.1218 |
0.416 |
|
| 1997 |
van Dijk GW, Wokke JH, Notermans NC, van den Berg LH, Bär PR. Indications for an immune-mediated etiology of idiopathic sensory neuronopathy. Journal of Neuroimmunology. 74: 165-72. PMID 9119970 DOI: 10.1016/S0165-5728(96)00225-1 |
0.327 |
|
| 1997 |
Wokke JH, van Dijk GW. Sensory neuropathies including painful and toxic neuropathies. Journal of Neurology. 244: 209-21. PMID 9112589 DOI: 10.1007/S004150050075 |
0.318 |
|
| 1997 |
Van den Berg LH, Lokhorst H, Wokke JH. Pulsed high-dose dexamethasone is not effective in patients with multifocal motor neuropathy. Neurology. 48: 1135. PMID 9109920 DOI: 10.1212/WNL.48.4.1135 |
0.396 |
|
| 1997 |
Weijnen F, van der Bilt A, van der Glas H, Bosman F, Wokke J. Oral muscle functions in patients with myasthenia gravis Neuromuscular Disorders. 7: 451-452. DOI: 10.1016/S0960-8966(97)87263-X |
0.327 |
|
| 1996 |
van der Kooi AJ, Barth PG, Busch HF, de Haan R, Ginjaar HB, van Essen AJ, van Hooff LJ, Höweler CJ, Jennekens FG, Jongen P, Oosterhuis HJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, et al. The clinical spectrum of limb girdle muscular dystrophy. A survey in The Netherlands. Brain : a Journal of Neurology. 119: 1471-80. PMID 8931572 DOI: 10.1093/Brain/119.5.1471 |
0.568 |
|
| 1996 |
Notermans NC, Lokhorst HM, Franssen H, Van der Graaf Y, Teunissen LL, Jennekens FG, Van den Berg LH, Wokke JH. Intermittent cyclophosphamide and prednisone treatment of polyneuropathy associated with monoclonal gammopathy of undetermined significance. Neurology. 47: 1227-33. PMID 8909434 DOI: 10.1212/Wnl.47.5.1227 |
0.643 |
|
| 1996 |
Notermans NC, Wokke JH, van den Berg LH, van der Graaf Y, Franssen H, Teunissen LL, Lokhorst HM. Chronic idiopathic axonal polyneuropathy. Comparison of patients with and without monoclonal gammopathy. Brain : a Journal of Neurology. 421-7. PMID 8800937 DOI: 10.1093/BRAIN/119.2.421 |
0.47 |
|
| 1996 |
Jennekens FG, de Visser M, Wintzen AR, Wokke JH. [For the present Duchenne' disease should not be treated with prednisone]. Nederlands Tijdschrift Voor Geneeskunde. 140: 1109-11. PMID 8692335 |
0.5 |
|
| 1996 |
Wokke JH, van den Berg LH, van Schaik JP. Sixth nerve palsy from a CNS lesion in chronic inflammatory demyelinating polyneuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 60: 695-6. PMID 8648345 DOI: 10.1136/jnnp.60.6.695 |
0.381 |
|
| 1995 |
Van den Berg LH, Franssen H, Wokke JH. Improvement of multifocal motor neuropathy during long-term weekly treatment with human immunoglobulin. Neurology. 45: 987-8. PMID 7746420 DOI: 10.1212/WNL.45.5.987 |
0.406 |
|
| 1995 |
Van den Berg LH, Mollee I, Wokke JH, Logtenberg T. Increased frequencies of HPRT mutant T lymphocytes in patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy: further evidence for a role of T cells in the etiopathogenesis of peripheral demyelinating diseases. Journal of Neuroimmunology. 58: 37-42. PMID 7730448 DOI: 10.1016/0165-5728(94)00185-Q |
0.634 |
|
| 1995 |
Van den Berg LH, Kerkhoff H, Oey PL, Franssen H, Mollee I, Vermeulen M, Jennekens FG, Wokke JH. Treatment of multifocal motor neuropathy with high dose intravenous immunoglobulins: a double blind, placebo controlled study. Journal of Neurology, Neurosurgery, and Psychiatry. 59: 248-52. PMID 7673950 DOI: 10.1136/Jnnp.59.3.248 |
0.626 |
|
| 1995 |
Wokke JH, Ausems MG, van den Boogaard MJ, Ippel EF, van Diggelene O, Kroos MA, Boer M, Jennekens FG, Reuser AJ, Ploos van Amstel HK. Genotype-phenotype correlation in adult-onset acid maltase deficiency. Annals of Neurology. 38: 450-4. PMID 7668832 DOI: 10.1002/Ana.410380316 |
0.588 |
|
| 1994 |
Harms L, Bock A, JÄnisch W, Valdueza J, Weber J, Link I, De Keyser J, Goossens A, Wilczak N, Vedeler C, Bjorge L, Uvestad E, Conti G, Williams K, Ginsberg L, ... ... Wokke JH, ... ... Wokke JH, et al. Fourth meeting of the European Neurological Society 25-29 June 1994 Barcelona, Spain : Abstracts of Symposia and free communications. Journal of Neurology. 241: 1-164. PMID 26553063 DOI: 10.1007/Bf02333089 |
0.45 |
|
| 1994 |
Notermans NC, Franssen H, Wieneke GH, Wokke JH. Temperature dependence of nerve conduction and EMG in neuropathy associated with gammopathy. Muscle & Nerve. 17: 516-22. PMID 8159182 DOI: 10.1002/Mus.880170508 |
0.337 |
|
| 1994 |
Notermans NC, Wokke JH, Franssen H, Vermeulen M, Busch HF, Jennekens FG. [Course of chronic idiopathic polyneuropathy during middle age and older: 2-year follow-up study]. Nederlands Tijdschrift Voor Geneeskunde. 138: 1281-5. PMID 8022510 |
0.583 |
|
| 1994 |
Notermans NC, Wokke JH, Lokhorst HM, Franssen H, van der Graaf Y, Jennekens FG. Polyneuropathy associated with monoclonal gammopathy of undetermined significance. A prospective study of the prognostic value of clinical and laboratory abnormalities. Brain : a Journal of Neurology. 117: 1385-93. PMID 7820574 DOI: 10.1093/Brain/117.6.1385 |
0.577 |
|
| 1994 |
Notermans NC, Wokke JH, van der Graaf Y, Franssen H, van Dijk GW, Jennekens FG. Chronic idiopathic axonal polyneuropathy: a five year follow up. Journal of Neurology, Neurosurgery, and Psychiatry. 57: 1525-7. PMID 7798984 DOI: 10.1136/Jnnp.57.12.1525 |
0.569 |
|
| 1994 |
van Dijk G, Wokke J, Notermans N, Bär P. Serum from patients with idiopathic sensory neuronopathy inhibits neurite outgrowth from embryonic dorsal root ganglia Journal of Neuroimmunology. 54: 157. DOI: 10.1016/0165-5728(94)90290-9 |
0.312 |
|
| 1994 |
Van den Berg L, Wokke J, Mollee I, Logtenberg T. In vivo frequency of mutant T cells in Guillain Barre syndrome and chronic inflammatory demyelinating polyneuropathy Journal of Neuroimmunology. 54: 152. DOI: 10.1016/0165-5728(94)90262-3 |
0.581 |
|
| 1993 |
van den Berg LH, Lankamp CL, de Jager AE, Notermans NC, Sodaar P, Marrink J, de Jong HJ, Bär PR, Wokke JH. Anti-sulphatide antibodies in peripheral neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 1164-8. PMID 8229027 DOI: 10.1136/jnnp.56.11.1164 |
0.444 |
|
| 1993 |
Notermans NC, Wokke JH, Franssen H, van der Graaf Y, Vermeulen M, van den Berg LH, Bär PR, Jennekens FG. Chronic idiopathic polyneuropathy presenting in middle or old age: a clinical and electrophysiological study of 75 patients. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 1066-71. PMID 7691991 DOI: 10.1136/Jnnp.56.10.1066 |
0.655 |
|
| 1992 |
Hesselmans LF, Jennekens FG, Kartman J, Wokke JH, de Visser M, Klaver-Krol EG, DeBaets M, Spaans F, Veldman H. Secondary changes of the motor endplate in Lambert-Eaton myasthenic syndrome: a quantitative study. Acta Neuropathologica. 83: 202-6. PMID 1557950 DOI: 10.1007/Bf00308480 |
0.548 |
|
| 1992 |
Notermans N, Wokke J, Franssen H, van der Graaf Y, Vermeulen M, van den Berg H, Jennekens F. 12. Chronic idiopathic neuropathy Clinical Neurology and Neurosurgery. 94: 83. DOI: 10.1016/0303-8467(92)90157-X |
0.494 |
|
| 1990 |
Jansen C, Jennekens FG, Wokke JH, Leppink GJ, Wijnne HJ. Lip-length and snout indices: methods for quantitative assessment of peri-oral facial muscle strength. Journal of the Neurological Sciences. 97: 133-42. PMID 2401893 DOI: 10.1016/0022-510X(90)90212-6 |
0.572 |
|
| 1990 |
Wokke JH, Jennekens FG, van den Oord CJ, Veldman H, Smit LM, Leppink GJ. Morphological changes in the human end plate with age. Journal of the Neurological Sciences. 95: 291-310. PMID 2358822 DOI: 10.1016/0022-510X(90)90076-Y |
0.565 |
|
| 1989 |
Wokke JH, Van den Oord CJ, Leppink GJ, Jennekens FG. Perisynaptic satellite cells in human external intercostal muscle: a quantitative and qualitative study. The Anatomical Record. 223: 174-80. PMID 2712344 DOI: 10.1002/Ar.1092230209 |
0.554 |
|
| 1989 |
Wokke JH, Jennekens FG, Molenaar PC, Van den Oord CJ, Oen BS, Busch HF. Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibs. Neurology. 39: 648-54. PMID 2710355 DOI: 10.1212/Wnl.39.5.648 |
0.59 |
|
| 1988 |
Wokke JH, Jennekens FG, van den Oord CJ, Veldman H, van Gijn J. Histological investigations of muscle atrophy and end plates in two critically ill patients with generalized weakness. Journal of the Neurological Sciences. 88: 95-106. PMID 3225632 DOI: 10.1016/0022-510X(88)90208-0 |
0.626 |
|
| 1988 |
Jennekens FG, Veldman H, Wokke JH, Smit LM, vd Oord CJ, Oen BS, Molenaar PC. Junctional plasticity in hereditary myasthenia. Monographs in Allergy. 25: 125-7. PMID 3173361 |
0.467 |
|
| 1988 |
Hoop RGvd, Neijt J, Jennekens F, Gispen W, Bär P, Wokke J, Jennekens F. Scientific meeting of the Amsterdamsche Neurologenvereeniging held in Amsterdam, 3rd December 1987 Clinical Neurology and Neurosurgery. 90: 183-184. DOI: 10.1016/S0303-8467(88)80047-7 |
0.586 |
|
| 1987 |
Jennekens FG, Wokke JH. Proximal weakness of the extremities as main feature of amyloid myopathy. Journal of Neurology, Neurosurgery, and Psychiatry. 50: 1353-8. PMID 3681315 |
0.531 |
|
| 1987 |
Wokke JH, de Koning J, Stanek G, Jennekens FG. Chronic muscle weakness caused by Borrelia burgdorferi meningoradiculitis. Annals of Neurology. 22: 389-92. PMID 3674804 DOI: 10.1002/ana.410220319 |
0.533 |
|
| 1987 |
Oosterhuis HJ, Newsom-Davis J, Wokke JH, Molenaar PC, Weerden TV, Oen BS, Jennekens FG, Veldman H, Vincent A, Wray DW. The slow channel syndrome. Two new cases. Brain : a Journal of Neurology. 110: 1061-79. PMID 3651795 DOI: 10.1093/Brain/110.4.1061 |
0.582 |
|
| 1987 |
Wokke JH, van Gijn J, Elderson A, Stanek G. Chronic forms of Borrelia burgdorferi infection of the nervous system. Neurology. 37: 1031-4. PMID 3587624 DOI: 10.1212/Wnl.37.6.1031 |
0.348 |
|
| 1987 |
Koudstaal PJ, Vermeulen M, Wokke JH. Argyll Robertson pupils in lymphocytic meningoradiculitis (Bannwarth's syndrome) Journal of Neurology, Neurosurgery, and Psychiatry. 50: 363-5. PMID 3559622 DOI: 10.1136/Jnnp.50.3.363 |
0.32 |
|
| Show low-probability matches. |
