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

LRRK2 and Parkin mutations in a family with parkinsonism—Lack of genotype-phenotype correlationMARRAS, Connie; KLEIN, Christine; BI, Andrew et al.Neurobiology of aging. 2010, Vol 31, Num 4, pp 721-722, issn 0197-4580, 2 p.Article

Clinical findings in a large family with a parkin Ex3Δ40 mutationMUNHOZ, Renato P; SA, Daniel S; ROGAEVA, Ekaterina et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 701-704, issn 0003-9942, 4 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

Variant Alzheimer's Disease with Spastic Paraparesis and Supranuclear Gaze PalsySINHA, Namita; GRIMES, David; TOKUHIRO, Shinya et al.Canadian journal of neurological sciences. 2013, Vol 40, Num 2, pp 249-251, issn 0317-1671, 3 p.Article

Investigation of C9orf72 in 4 Neurodegenerative DisordersZHENGRUI XI; ZINMAN, Lome; MORON, Francisco J et al.Archives of neurology (Chicago). 2012, Vol 69, Num 12, pp 1583-1590, issn 0003-9942, 8 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

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

T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson diseaseCHISHTI, Muhammad A; BOHLEGA, Saeed; AHMED, Maqbool et al.Archives of neurology (Chicago). 2006, Vol 63, Num 10, pp 1483-1485, issn 0003-9942, 3 p.Article

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