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au.\*:("KAWARAI, Toshitaka")

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TMP21 is a presenilin complex component that modulates γ-secretase but not ε-secretase activityFUSHENG CHEN; HASEGAWA, Hiroshi; WAKUTANI, Yosuke et al.Nature (London). 2006, Vol 440, Num 7088, pp 1208-1212, issn 0028-0836, 5 p.Article

Accumulation of filamentous tau in the cerebral cortex of human tau R406W transgenic miceIKEDA, Masaki; SHOJI, Mikio; ISHIGURO, Koichi et al.The American journal of pathology. 2005, Vol 166, Num 2, pp 521-531, issn 0002-9440, 11 p.Article

Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin geneORLACCHIO, Antonio; KAWARAI, Toshitaka; POLIDORO, Mario et al.Neuroscience letters. 2004, Vol 363, Num 1, pp 49-53, issn 0304-3940, 5 p.Article

Benign hereditary chorea: Clinical, genetic, and pathological findingsKLEINER-FISMAN, Galit; ROGAEVA, Ekaterina; HALLIDAY, William et al.Annals of neurology. 2003, Vol 54, Num 2, pp 244-247, issn 0364-5134, 4 p.Article

Childhood onset in familial prion disease with a novel mutation in the PRNP geneROGAEVA, Ekaterina; ZADIKOFF, Cindy; PONESSE, Jonathan et al.Archives of neurology (Chicago). 2006, Vol 63, Num 7, pp 1016-1021, issn 0003-9942, 6 p.Article

New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1ORLACCHIO, Antonio; KAWARAI, Toshitaka; GAUDIELLO, Fabrizio et al.Annals of neurology. 2005, Vol 58, Num 3, pp 423-429, issn 0364-5134, 7 p.Article

No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been foundJOHNSON, Janel; OSTOJIC, Jovanka; PASTOR, Pau et al.Neuroscience letters. 2004, Vol 363, Num 2, pp 99-101, issn 0304-3940, 3 p.Article

Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin I causes increased Aβ42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegansDONG MEI ZHANG; LEVITAN, Diane; ROGAEVA, Ekaterina et al.Neuroreport (Oxford). 2000, Vol 11, Num 14, pp 3227-3230, issn 0959-4965Article

Defects in the striatal neuropeptide Y system in X-linked dystonia-parkinsonismGOTO, Satoshi; KAWARAI, Toshitaka; MORIGAKI, Ryoma et al.Brain. 2013, Vol 136, pp 1555-1567, issn 0006-8950, 13 p., 5Article

Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's diseaseSHIBATA, Nobuto; KAWARAI, Toshitaka; ROGAEVA, Ekaterina et al.Neuroscience letters. 2005, Vol 391, Num 3, pp 142-146, issn 0304-3940, 5 p.Article

Analysis of the glucocerebrosidase gene in Parkinson's diseaseSATO, Christine; MORGAN, Angharad; LANG, Anthony E et al.Movement disorders. 2004, Vol 20, Num 3, pp 367-370, issn 0885-3185, 4 p.Article

Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tanglesTANDON, Anurag; HAUNG YU; FRASER, Paul E et al.Journal of neurochemistry. 2003, Vol 86, Num 3, pp 572-581, issn 0022-3042, 10 p.Article

Late-onset CMT2 associated with a novel missense mutation in the cytoplasmic domain of the MPZ geneSHIMIZU, Hirotaka; OKA, Nobuyuki; KAWARAI, Toshitaka et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2010, Vol 112, Num 9, pp 798-800, issn 0303-8467, 3 p.Article

The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant InvolvementISHIURA, Hiroyuki; SAKO, Wataru; ICHIKAWA, Yaeko et al.American journal of human genetics. 2012, Vol 91, Num 2, pp 320-329, issn 0002-9297, 10 p.Article

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosisORLACCHIO, Antonio; BABALINI, Carla; KAWARAI, Toshitaka et al.Brain. 2010, Vol 133, pp 591-598, issn 0006-8950, 8 p., 2Article

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer diseaseROGAEVA, Ekaterina; YAN MENG; FUSHENG CHEN et al.Nature genetics. 2007, Vol 39, Num 2, pp 168-177, issn 1061-4036, 10 p.Article

Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)MUNHOZ, Renato P; KAWARAI, Toshitaka; TEIVE, Helio A et al.Movement disorders. 2006, Vol 21, Num 2, pp 279-281, issn 0885-3185, 3 p.Article

Novel SPG6 mutation p.A100T in a japanese family with autosomal dominant form of hereditary spastic paraplegiaKANEKO, Satoshi; KAWARAI, Toshitaka; ST GEORGE-HYSLOP, Peter et al.Movement disorders. 2006, Vol 21, Num 9, pp 1531-1533, issn 0885-3185, 3 p.Article

Clinical and genetic study of a large SPG4 Italian familyORLACCHIO, Antonio; KAWARAI, Toshitaka; GAUDIELLO, Fabrizio et al.Movement disorders. 2005, Vol 20, Num 8, pp 1055-1059, issn 0885-3185, 5 p.Article

Conversion to dementia among two groups with cognitive impairment: A preliminary reportLUIS, Cheryl A; BARKER, Warren W; LOEWENSTEIN, David A et al.Dementia and geriatric cognitive disorders. 2004, Vol 18, Num 3-4, pp 307-313, issn 1420-8008, 7 p.Article

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