| Year |
Citation |
Score |
| 2020 |
Chen Z, Yan Yau W, Jaunmuktane Z, Tucci A, Sivakumar P, Gagliano Taliun SA, Turner C, Efthymiou S, Ibáñez K, Sullivan R, Bibi F, Athanasiou-Fragkouli A, Bourinaris T, Zhang D, Revesz T, ... ... Haltia MJ, et al. Neuronal intranuclear inclusion disease is genetically heterogeneous. Annals of Clinical and Translational Neurology. PMID 32777174 DOI: 10.1002/Acn3.51151 |
0.35 |
|
| 2013 |
Kiuru-Enari SMK, Haltia M. Hereditary gelsolin amyloidosis. Handbook of Clinical Neurology. 115: 659-681. PMID 23931809 DOI: 10.1016/B978-0-444-52902-2.00039-4 |
0.313 |
|
| 2013 |
Haltia M, Goebel HH. The neuronal ceroid-lipofuscinoses: a historical introduction. Biochimica Et Biophysica Acta. 1832: 1795-800. PMID 22959893 DOI: 10.1016/J.Bbadis.2012.08.012 |
0.383 |
|
| 2009 |
Airaksinen EM, Iivanainen M, Karli P, Sainio K, Haltia M. Hereditary recurrent brachial plexus neuropathy with dysmorphic features. Acta Neurologica Scandinavica. 71: 309-316. PMID 4003034 DOI: 10.1111/J.1600-0404.1985.Tb03205.X |
0.317 |
|
| 2009 |
Haltia M, Tarkkanen A, Somer H, Palo J, Karli H. Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmologica. 64: 637-643. PMID 3028034 DOI: 10.1111/J.1755-3768.1986.Tb00680.X |
0.346 |
|
| 2009 |
Sulkava R, Haltia M, Paetau A, Wikström J, Palo J. Clinical And Neuropathological Features In Alzheimer'S Disease Acta Neurologica Scandinavica. 65: 294-295. DOI: 10.1111/J.1600-0404.1982.Tb03495.X |
0.323 |
|
| 2009 |
Koskiniemi M, Donner M, Majuri H, Haltia M, Norio R. Progressive myoclonus epilepsy. A clinical and histopathological study. Acta Neurologica Scandinavica. 50: 307-332. DOI: 10.1111/J.1600-0404.1974.Tb02782.X |
0.337 |
|
| 2008 |
Santavuori P, Haltia M, Rapola J. Infantile Type of So‐called Neuronal Ceroid‐lipofuscinosis Developmental Medicine & Child Neurology. 16: 644-653. PMID 4371326 DOI: 10.1111/J.1469-8749.1974.Tb04183.X |
0.318 |
|
| 2008 |
Salonen R, Somer M, Haltia M, Lorentz M, Norio R. Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome). Clinical Genetics. 39: 287-293. PMID 2070547 DOI: 10.1111/J.1399-0004.1991.Tb03027.X |
0.34 |
|
| 2006 |
Haltia M. The neuronal ceroid-lipofuscinoses: from past to present. Biochimica Et Biophysica Acta. 1762: 850-856. PMID 16908122 DOI: 10.1016/J.Bbadis.2006.06.010 |
0.402 |
|
| 2006 |
Siintola E, Partanen S, Strömme P, Haapanen A, Haltia M, Maehlen J, Lehesjoki AE, Tyynelä J. Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis. Brain : a Journal of Neurology. 129: 1438-45. PMID 16670177 DOI: 10.1093/Brain/Awl107 |
0.351 |
|
| 2005 |
Myllykangas L, Tyynelä J, Page-McCaw A, Rubin GM, Haltia MJ, Feany MB. Cathepsin D-deficient Drosophila recapitulate the key features of neuronal ceroid lipofuscinoses. Neurobiology of Disease. 19: 194-9. PMID 15837574 DOI: 10.1016/J.Nbd.2004.12.019 |
0.331 |
|
| 2005 |
Kiuru-Enari S, Keski-Oja J, Haltia M. Cutis laxa in hereditary gelsolin amyloidosis British Journal of Dermatology. 152: 250-257. PMID 15727635 DOI: 10.1111/J.1365-2133.2004.06276.X |
0.359 |
|
| 2004 |
Tyynelä J, Cooper JD, Khan MN, Shemilts SJ, Haltia M. Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activation. Brain Pathology (Zurich, Switzerland). 14: 349-57. PMID 15605981 DOI: 10.1111/J.1750-3639.2004.Tb00077.X |
0.353 |
|
| 2004 |
Verkkoniemi A, Ylikoski R, Rinne JO, Somer M, Hietaharju A, Erkinjuntti T, Viitanen M, Kalimo H, Haltia M. Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis. Journal of the Neurological Sciences. 218: 29-37. PMID 14759630 DOI: 10.1016/J.Jns.2003.10.020 |
0.324 |
|
| 2003 |
Paloneva J, Mandelin J, Kiialainen A, Böhling T, Prudlo J, Hakola P, Haltia M, Konttinen YT, Peltonen L. DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features. Journal of Experimental Medicine. 198: 669-675. PMID 12925681 DOI: 10.1084/Jem.20030027 |
0.305 |
|
| 2003 |
Haltia M. The Neuronal Ceroid-Lipofuscinoses Journal of Neuropathology and Experimental Neurology. 62: 1-13. PMID 12528813 DOI: 10.1093/Jnen/62.1.1 |
0.39 |
|
| 2002 |
Kiuru-Enari S, Somer H, Seppäläinen A, Notkola I, Haltia M. Neuromuscular pathology in hereditary gelsolin amyloidosis. Journal of Neuropathology and Experimental Neurology. 61: 565-571. PMID 12071640 DOI: 10.1093/Jnen/61.6.565 |
0.319 |
|
| 2002 |
Myllykangas L, Polvikoski T, Reunanen K, Wavrant-De Vrieze F, Ellis C, Hernandez D, Sulkava R, Kontula K, Verkkoniemi A, Notkola IL, Hardy J, Perez-Tur J, Haltia MJ, Tienari PJ. ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain. American Journal of Medical Genetics. 114: 288-91. PMID 11920850 DOI: 10.1002/Ajmg.10202 |
0.31 |
|
| 2001 |
Haltia M, Herva R, Suopanki J, Baumann M, Tyynelä J. Hippocampal lesions in the neuronal ceroid lipofuscinoses. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 5: 209-11. PMID 11588999 DOI: 10.1053/Eipn.2000.0464 |
0.313 |
|
| 2001 |
Mann DM, Takeuchi A, Sato S, Cairns NJ, Lantos PL, Rossor MN, Haltia M, Kalimo H, Iwatsubo T. Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques. Neuropathology and Applied Neurobiology. 27: 189-96. PMID 11489138 DOI: 10.1046/J.1365-2990.2001.00316.X |
0.31 |
|
| 2001 |
Verkkoniemi A, Kalimo H, Paetau A, Somer M, Iwatsubo T, Hardy J, Haltia M. Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype. Journal of Neuropathology and Experimental Neurology. 60: 483-92. PMID 11379823 DOI: 10.1093/Jnen/60.5.483 |
0.353 |
|
| 2001 |
Ranta S, Savukoski M, Santavuori P, Haltia M. 6 Studies of homogenous populations: CLN5 and CLN8 Advances in Genetics. 45: 123-140. PMID 11332769 DOI: 10.1016/S0065-2660(01)45007-3 |
0.327 |
|
| 2000 |
Haltia M. Human prion diseases. Annals of Medicine. 32: 493-500. PMID 11087170 DOI: 10.3109/07853890009002025 |
0.315 |
|
| 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, ... ... Haltia M, 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 |
0.376 |
|
| 2000 |
Myllykangas L, Polvikoski T, Sulkava R, Verkkoniemi A, Tienari P, Niinistö L, Kontula K, Hardy J, Haltia M, Pérez-Tur J. Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over. Neuroscience Letters. 292: 195-8. PMID 11018310 DOI: 10.1016/S0304-3940(00)01467-1 |
0.336 |
|
| 2000 |
Tyynelä J, Sohar I, Sleat DE, Gin RM, Donnelly RJ, Baumann M, Haltia M, Lobel P. A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration. The Embo Journal. 19: 2786-92. PMID 10856224 DOI: 10.1093/Emboj/19.12.2786 |
0.359 |
|
| 2000 |
Baker M, Graff-Radford D, Wavrant DeVrièze F, Graff-Radford N, Petersen RC, Kokmen E, Boeve B, Myllykangas L, Polvikoski T, Sulkava R, Verkoniemmi A, Tienari P, Haltia M, Hardy J, Hutton M, et al. No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease. Neuroscience Letters. 285: 147-9. PMID 10793248 DOI: 10.1016/S0304-3940(00)01057-0 |
0.337 |
|
| 2000 |
Herva R, Tyynelä J, Hirvasniemi A, Syrjäkallio-Ylitalo M, Haltia M. Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis. Brain Pathology (Zurich, Switzerland). 10: 215-22. PMID 10764041 DOI: 10.1111/J.1750-3639.2000.Tb00255.X |
0.344 |
|
| 2000 |
Auranen M, Rapola J, Pihko H, Haltia M, Leivo I, Soinila S, Virtanen I, Kalimo H, Anderson LV, Santavuori P, Somer H. Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease. Neuromuscular Disorders : Nmd. 10: 16-23. PMID 10677859 DOI: 10.1016/S0960-8966(99)00066-8 |
0.312 |
|
| 2000 |
Verkkoniemi A, Somer M, Rinne J, Myllykangas L, Kalimo H, Haltia M. Clinical characterization of variant Alzheimer's disease with spastic paraparesis Neurobiology of Aging. 21: 234. DOI: 10.1016/S0197-4580(00)83389-8 |
0.333 |
|
| 1999 |
Prihar G, Verkkoniem A, Perez-Tur J, Crook R, Lincoln S, Houlden H, Somer M, Paetau A, Kalimo H, Grover A, Myllykangas L, Hutton M, Hardy J, Haltia M. Alzheimer disease PS-1 exon 9 deletion defined. Nature Medicine. 5: 1090. PMID 10502791 DOI: 10.1038/13383 |
0.332 |
|
| 1999 |
Uusitalo A, Tenhunen K, Heinonen O, Hiltunen JO, Saarma M, Haltia M, Jalanko A, Peltonen L. Toward understanding the neuronal pathogenesis of aspartylglucosaminuria: Expression of aspartylglucosaminidase in brain during development Molecular Genetics and Metabolism. 67: 294-307. PMID 10444340 DOI: 10.1006/Mgme.1999.2872 |
0.346 |
|
| 1999 |
Suopanki J, Tyynelä J, Baumann M, Haltia M. Palmitoyl-protein thioesterase, an enzyme implicated in neurodegeneration, is localized in neurons and is developmentally regulated in rat brain. Neuroscience Letters. 265: 53-6. PMID 10327204 DOI: 10.1016/S0304-3940(99)00207-4 |
0.339 |
|
| 1999 |
Suopanki J, Tyynelä J, Baumann M, Haltia M. The expression of palmitoyl-protein thioesterase is developmentally regulated in neural tissues but not in nonneural tissues. Molecular Genetics and Metabolism. 66: 290-3. PMID 10191117 DOI: 10.1006/Mgme.1999.2839 |
0.332 |
|
| 1999 |
Kiuru S, Salonen O, Haltia M. Gelsolin-related spinal and cerebral amyloid angiopathy. Annals of Neurology. 45: 305-311. PMID 10072044 DOI: 10.1002/1531-8249(199903)45:3<305::Aid-Ana5>3.0.Co;2-E |
0.331 |
|
| 1999 |
Myllykangas L, Polvikoski T, Sulkava R, Verkkoniemi A, Crook R, Tienari PJ, Pusa A, Niinistö L, O'Brien P, Kontula K, Hardy J, Haltia M, Pérez‐Tur J. Genetic association of α2‐macroglobulin with Alzheimer's disease in a Finnish elderly population Annals of Neurology. 46: 382-390. DOI: 10.1002/1531-8249(199909)46:3<382::Aid-Ana14>3.0.Co;2-5 |
0.353 |
|
| 1998 |
Crook R, Verkkoniemi A, Perez-Tur J, Mehta N, Baker M, Houlden H, Farrer M, Hutton M, Lincoln S, Hardy J, Gwinn K, Somer M, Paetau A, Kalimo H, Ylikoski R, ... ... Haltia M, et al. A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nature Medicine. 4: 452-5. PMID 9546792 DOI: 10.1038/Nm0498-452 |
0.381 |
|
| 1997 |
Autti T, Raininko R, Haltia M, Lauronen L, Vanhanen S, Salonen O, Aronen HJ, Wirtavuori K, Santavuori P. Aspartylglucosaminuria: radiologic course of the disease with histopathologic correlation Journal of Child Neurology. 12: 369-375. PMID 9309520 DOI: 10.1177/088307389701200606 |
0.313 |
|
| 1997 |
Autti T, Raininko R, Santavuori P, Vanhanen S, Poutanen VP, Haltia M. MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type. Neuroradiology. 39: 371-377. PMID 9189886 DOI: 10.1007/S002340050427 |
0.339 |
|
| 1997 |
Suomalainen A, Majander A, Wallin M, Setälä K, Kontula K, Leinonen H, Salmi T, Paetau A, Haltia M, Valanne L, Lonnqvist J, Peltonen L, Somer H. Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease. Neurology. 48: 1244-53. PMID 9153451 DOI: 10.1212/Wnl.48.5.1244 |
0.344 |
|
| 1997 |
Tyynelä J, Suopanki J, Baumann M, Haltia M. Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL). Neuropediatrics. 28: 49-52. PMID 9151322 DOI: 10.1055/S-2007-973667 |
0.317 |
|
| 1997 |
Tyynelä J, Suopanki J, Santavuori P, Baumann M, Haltia M. Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry. Journal of Neuropathology and Experimental Neurology. 56: 369-75. PMID 9100667 DOI: 10.1097/00005072-199704000-00005 |
0.366 |
|
| 1997 |
Haltia M, Leivo I, Somer H, Pihko H, Paetau A, Kivelä T, Tarkkanen A, Tomé F, Engvall E, Santavuori P. Muscle-eye-brain disease: a neuropathological study. Annals of Neurology. 41: 173-80. PMID 9029066 DOI: 10.1002/Ana.410410208 |
0.365 |
|
| 1996 |
Erkinjuntti T, Benavente O, Eliasziw M, Munoz DG, Sulkava R, Haltia M, Hachinski V. Diffuse vacuolization (spongiosis) and arteriolosclerosis in the frontal white matter occurs in vascular dementia. Archives of Neurology. 53: 325-32. PMID 8929154 DOI: 10.1001/Archneur.1996.00550040053014 |
0.343 |
|
| 1996 |
Goebel HH, Gerhard L, Kominami E, Haltia M. Neuronal ceroid-lipofuscinosis--late-infantile or Jansky-Bielschowsky type--revisited. Brain Pathology (Zurich, Switzerland). 6: 225-8. PMID 8864279 DOI: 10.1111/J.1750-3639.1996.Tb00850.X |
0.319 |
|
| 1996 |
Mann DM, Iwatsubo T, Cairns NJ, Lantos PL, Nochlin D, Sumi SM, Bird TD, Poorkaj P, Hardy J, Hutton M, Prihar G, Crook R, Rossor MN, Haltia M. Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43). Annals of Neurology. 40: 149-56. PMID 8773595 DOI: 10.1002/Ana.410400205 |
0.314 |
|
| 1996 |
Sulkava R, Kainulainen K, Verkkoniemi A, Niinistö L, Sobel E, Davanipour Z, Polvikoski T, Haltia M, Kontula K. APOE Alleles in Alzheimer's Disease and Vascular Dementia in a Population Aged 85+ Neurobiology of Aging. 17: 373-376. PMID 8725898 DOI: 10.1016/0197-4580(96)00023-1 |
0.328 |
|
| 1995 |
Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Jellinger K. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathology (Zurich, Switzerland). 5: 459-66. PMID 8974629 DOI: 10.1111/J.1750-3639.1995.Tb00625.X |
0.392 |
|
| 1995 |
Haltia M, Tyynelä J, Baumann M, Henseler M, Sandhoff K. Immunological studies on sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses. Gerontology. 41: 239-48. PMID 8821335 DOI: 10.1159/000213746 |
0.345 |
|
| 1995 |
Vanhanen S, Raininko R, Santavuori P, Autti T, Haltia M. MRI evaluation of the brain in infantile neuronal ceroid-lipofuscinosis. Part 1: Postmortem MRI with histopathologic correlation. Journal of Child Neurology. 10: 438-443. PMID 8576552 DOI: 10.1177/088307389501000603 |
0.347 |
|
| 1995 |
Tyynelä J, Baumann M, Henseler M, Sandhoff K, Haltia M. Sphingolipid activator proteins (SAPs) are stored together with glycosphingolipids in the infantile neuronal ceroid-lipofuscinosis (INCL). American Journal of Medical Genetics. 57: 294-7. PMID 7668348 DOI: 10.1002/Ajmg.1320570236 |
0.322 |
|
| 1995 |
Brown P, Kenney K, Little B, Ironside J, Will R, Cervenáková L, Bjork RJ, San Martin RA, Safar J, Roos R, Haltia M, Gibbs CJ, Gajdusek DC. Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy Annals of Neurology. 38: 245-253. PMID 7654073 DOI: 10.1002/Ana.410380218 |
0.364 |
|
| 1995 |
Tyynelä J, Baumann M, Henseler M, Sandhoff K, Haltia M. Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study. Acta Neuropathologica. 89: 391-8. PMID 7618436 DOI: 10.1007/Bf00307641 |
0.358 |
|
| 1995 |
Polvikoski T, Sulkava R, Haltia M, Kainulainen K, Vuorio A, Verkkoniemi A, Niinistö L, Halonen P, Kontula K. Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein. The New England Journal of Medicine. 333: 1242-1247. PMID 7566000 DOI: 10.1056/Nejm199511093331902 |
0.315 |
|
| 1994 |
Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R, Goate A, Clark R, Korenblat K, Pandit S, Keller HD, et al. Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description Annals of Neurology. 36: 362-367. PMID 8080244 DOI: 10.1002/Ana.410360307 |
0.38 |
|
| 1994 |
Kiuru S, Matikainen E, Kupari M, Haltia M, Palo J. Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF) Journal of the Neurological Sciences. 126: 40-48. PMID 7836945 DOI: 10.1016/0022-510X(94)90092-2 |
0.332 |
|
| 1993 |
Haltia M, Somer M. Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). Acta Neuropathologica. 85: 241-247. PMID 8460530 DOI: 10.1007/Bf00227717 |
0.332 |
|
| 1993 |
Tyynelä J, Palmer DN, Baumann M, Haltia M. Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis. Febs Letters. 330: 8-12. PMID 8370464 DOI: 10.1016/0014-5793(93)80908-D |
0.334 |
|
| 1993 |
Kivelä T, Tarkkanen A, McLean I, Ghiso J, Frangione B, Haltia M. Immunohistochemical analysis of lattice corneal dystrophies types I and II. The British Journal of Ophthalmology. 77: 799-804. PMID 8110676 DOI: 10.1136/Bjo.77.12.799 |
0.305 |
|
| 1992 |
Suomalainen A, Majander A, Haltia M, Somer H, Lönnqvist J, Savontaus ML, Peltonen L. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. Journal of Clinical Investigation. 90: 61-66. PMID 1634620 DOI: 10.1172/Jci115856 |
0.314 |
|
| 1992 |
Hall NA, Thomas-Oates JE, Dell A, Haltia M, Lake BD, Patrick AD. Stored dolichyl pyrophosphoryl oligosaccharides in Batten disease. American Journal of Medical Genetics. 42: 580-5. PMID 1609839 DOI: 10.1002/Ajmg.1320420431 |
0.337 |
|
| 1992 |
Järvelä I, Santavuori P, Puhakka L, Haltia M, Peltonen L. Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1p. American Journal of Medical Genetics. 42: 546-548. PMID 1609836 DOI: 10.1002/Ajmg.1320420425 |
0.337 |
|
| 1992 |
Palmer DN, Fearnley IM, Walker JE, Hall NA, Lake BD, Wolfe LS, Haltia M, Martinus RD, Jolly RD. Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease). American Journal of Medical Genetics. 42: 561-7. PMID 1535179 DOI: 10.1002/Ajmg.1320420428 |
0.306 |
|
| 1992 |
Goldfarb LG, Brown P, Haltia M, Cathala F, McCombie WR, Kovanen J, Cervenáková L, Goldin L, Nieto A, Godec MS. Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin. Annals of Neurology. 31: 274-81. PMID 1353341 DOI: 10.1002/Ana.410310308 |
0.316 |
|
| 1992 |
Haltia M, Suomalainen A, Majander A, Somer H. Disorders Associated with Multiple Deletions of Mitochondrial DNA Brain Pathology. 2: 133-139. PMID 1341954 DOI: 10.1111/J.1750-3639.1992.Tb00681.X |
0.305 |
|
| 1991 |
Haltia M, Kovanen J, Goldfarb LG, Brown P, Gajdusek DC. Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies. European Journal of Epidemiology. 7: 494-500. PMID 1684756 DOI: 10.1007/Bf00143128 |
0.352 |
|
| 1990 |
Ghiso J, Haltia M, Prelli F, Novello J, Frangione B. Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type. The Biochemical Journal. 272: 827-30. PMID 2176481 DOI: 10.1042/Bj2720827 |
0.319 |
|
| 1990 |
Wisniewski KE, Maslinska D, Kitaguchi T, Kim KS, Goebel HH, Haltia M. Topographic heterogeneity of amyloid B-protein epitopes in brains with various forms of neuronal ceroid lipofuscinoses suggesting defective processing of amyloid precursor protein. Acta Neuropathologica. 80: 26-34. PMID 1694383 DOI: 10.1007/Bf00294218 |
0.389 |
|
| 1989 |
Haltia M. The hard core of Alzheimer's disease. Annals of Medicine. 21: 67. PMID 2765254 DOI: 10.3109/07853898909149185 |
0.312 |
|
| 1988 |
Roine RO, Hillrom M, Valle M, Haltia M, Ketonen L, Neuvonen E, Lumio J, Lähdevirta J. Fatal encephalitis caused by a bat-borne rabies-related virus. Clinical findings. Brain. 111: 1505-1516. PMID 3208067 DOI: 10.1093/Brain/111.6.1505 |
0.3 |
|
| 1988 |
Wolfe LS, Gauthier S, Haltia M, Palo J. Dolichol and dolichyl phosphate in the neuronal ceroid-lipofuscinoses and other diseases. American Journal of Medical Genetics. Supplement. 5: 233-42. PMID 3146321 DOI: 10.1002/Ajmg.1320310626 |
0.361 |
|
| 1985 |
Paetau A, Elovaara I, Paasivuo R, Virtanen I, Palo J, Haltia M. Glial filaments are a major brain fraction in infantile neuronal ceroid-lipofuscinosis. Acta Neuropathologica. 65: 190-94. PMID 4038838 DOI: 10.1007/Bf00686997 |
0.352 |
|
| 1985 |
Kovanen J, Erkinjuntti T, Iivanainen M, Ketonen L, Haltia M, Sulkava R, Sipponen JT. Cerebral MR and CT imaging in Creutzfeldt-Jakob disease. Journal of Computer Assisted Tomography. 9: 125-128. PMID 3881486 DOI: 10.1097/00004728-198501000-00023 |
0.302 |
|
| 1984 |
Palo J, Haltia M, Carpenter S, Karpati G, Mushynski W. Neurofilament subunit-related proteins in neuronal intranuclear inclusions Annals of Neurology. 15: 322-328. PMID 6331276 DOI: 10.1002/Ana.410150404 |
0.328 |
|
| 1984 |
Haltia M, Somer H, Palo J, Johnson WG. Neuronal intranuclear inclusion disease in identical twins Annals of Neurology. 15: 316-321. PMID 6331275 DOI: 10.1002/Ana.410150403 |
0.367 |
|
| 1983 |
Ng Ying Kin NM, Palo J, Haltia M, Wolfe LS. High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence. Journal of Neurochemistry. 40: 1465-73. PMID 6834069 DOI: 10.1111/J.1471-4159.1983.Tb13592.X |
0.383 |
|
| 1983 |
Wolfe LS, Ng Ying Kin NM, Palo J, Haltia M. Dolichols in brain and urinary sediment in neuronal ceroid lipofuscinosis. Neurology. 33: 103-6. PMID 6681549 DOI: 10.1212/Wnl.33.1.103 |
0.37 |
|
| 1983 |
Wood PL, Etienne P, Lal S, Nair NP, Finlayson MH, Gauthier S, Palo J, Haltia M, Paetau A, Bird ED. A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease. Journal of the Neurological Sciences. 62: 211-7. PMID 6142096 DOI: 10.1016/0022-510X(83)90200-9 |
0.351 |
|
| 1983 |
Wood PL, Nair NP, Etienne P, Lal S, Gauthier S, Robitaille Y, Bird ED, Palo J, Haltia M, Paetau A. Lack of cholinergic deficit in the neocortex in Pick's disease. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 7: 725-7. PMID 6141615 DOI: 10.1016/0278-5846(83)90053-2 |
0.318 |
|
| 1982 |
Wolfe LS, Ng Ying Kin NM, Palo J, Haltia M. Raised levels of cerebral cortex dolichols in Alzheimer's disease. Lancet (London, England). 2: 99. PMID 6123835 DOI: 10.1016/S0140-6736(82)91717-2 |
0.31 |
|
| 1981 |
Peter C, Maury J, Haltia M, Palo J. Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria Journal of the Neurological Sciences. 50: 291-298. PMID 6164750 DOI: 10.1016/0022-510X(81)90174-X |
0.319 |
|
| 1980 |
Kovanen J, Tiilikainen A, Haltia M. Histocompatibility antigens in familial Creutzfeldt-Jakob disease. Journal of the Neurological Sciences. 45: 317-321. PMID 6988548 DOI: 10.1016/0022-510X(80)90174-4 |
0.314 |
|
| 1980 |
Koskiniemi M, Vaheri A, Manninen V, Valtonen S, Ketonen L, Taskinen E, Sainio K, Karli P, Haltia M. Herpes Simplex Virus Encephalitis New Diagnostic and Clinical Features and Results of Therapy Jama Neurology. 37: 763-767. PMID 6255909 DOI: 10.1001/Archneur.1980.00500610043006 |
0.303 |
|
| 1980 |
Haltia T, Palo J, Haltia M, Icén A. Juvenile Metachromatic Leukodystrophy: Clinical, Biochemical, and Neuropathologic Studies in Nine New Cases Jama Neurology. 37: 42-46. PMID 6101304 DOI: 10.1001/Archneur.1980.00500500072011 |
0.329 |
|
| 1979 |
Haltia M, Kovanen J, Van Crevel H, Bots GT, Stefanko S. Familial Creutzfeldt-Jakob disease. Journal of the Neurological Sciences. 42: 381-9. PMID 390100 DOI: 10.1016/0022-510X(79)90171-0 |
0.383 |
|
| 1977 |
Haltia M, Paetau A, Vaheri A, Erkkilä H, Donner M, Kaakinen K, Holmström T. Fatal measles encephalopathy with retinopathy during cytotoxic chemotherapy. Journal of the Neurological Sciences. 32: 323-30. PMID 886358 DOI: 10.1016/0022-510X(77)90015-6 |
0.309 |
|
| 1976 |
Kahma K, Brotherus J, Haltia M, Renkonen O. Low and moderate concentrations of lysobisphosphatidic acid in brain and liver of patients affected by some storage diseases. Lipids. 11: 539-544. PMID 948249 DOI: 10.1007/Bf02532899 |
0.302 |
|
| 1975 |
Haltia M, Palo J, Autio S. Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies. Acta Neuropathologica. 31: 243-255. PMID 1138532 DOI: 10.1007/Bf00684563 |
0.334 |
|
| 1974 |
Santavuori P, Haltia M, Rapola J, Raitta C, Keranen A. Infantile Type of So-Called Neuronal Ceroid-Lipofuscinosis Acta Geneticae Medicae Et Gemellologiae. 23: 197-200. DOI: 10.1017/S1120962300023763 |
0.375 |
|
| 1973 |
Haltia M, Rapola J, Santavuori P. Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies. Acta Neuropathologica. 26: 157-170. PMID 4763201 DOI: 10.1007/Bf00697751 |
0.405 |
|
| 1973 |
Santavuori P, Haltia M, Rapola J, Raitta C. Infantile type of so-called neuronal ceroid-lipofuscinosis Journal of the Neurological Sciences. 18: 257-267. PMID 4698309 DOI: 10.1016/0022-510X(73)90075-0 |
0.368 |
|
| 1973 |
Haltia M, Rapola J, Santavuori P, Keränen A. Infantile type of so-called neuronal ceroid-lipofuscinosis: Part 2. Morphological and biochemical studies☆ Journal of the Neurological Sciences. 18: 269-285. PMID 4121459 DOI: 10.1016/0022-510X(73)90076-2 |
0.371 |
|
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