Screening for PS1 mutations in a referral-based series of AD cases: 21 Novel mutations
- Author
- ROGAEVA, E. A1 ; FAFEL, K. C2 ; MESCHINO, W1 6 ; ROCKWOOD, K7 ; BOSS, M. A2 ; MAYEUX, R8 ; GEORGE-HYSLOP, P. St1 ; SONG, Y. Q1 ; MEDEIROS, H1 ; SATO, C1 ; LIANG, Y1 ; RICHARD, E1 ; ROGAEV, E. I1 3 ; FROMMELT, P4 ; SADOVNICK, A. D5
[1] Centre for Research in Neurodegenerative Diseases and Division of Neurology, Department of Medicine, The University Health Network, Toronto, Ontario, Canada
[2] Athena Diagnostics Inc., Worcester, MA, United States
[3] Mental Health Research Center, Russian Academy of Medical Sciences, Moscow, Russian Federation
[4] Asklepios Klinik Schaufling, Department of Neurological Rehabilitation, Bavaria, Germany
[5] Departments of Medical Genetics and Medicine, Vancouver, British Columbia, Canada
[6] Department of Medical Genetics, North York General Hospital, North York, Ontario, Canada
[7] Division of Geriatric Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
[8] Taub Institute for Research on Alzheimer's Disease and the Aging Brain, New York, NY, United States - Source
Neurology. 2001, Vol 57, Num 4, pp 621-625 ; ref : 26 ref
- Publisher
- Lippincott Williams & Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- Russian
- Keyword (fr)
- Diagnostic Démence Alzheimer Dépistage Déterminisme génétique Gène Homme Mutation Polymorphisme Préséniline Encéphale pathologie Maladie dégénérative Maladie héréditaire Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Diagnosis Alzheimer disease Medical screening Genetic determinism Gene Human Mutation Polymorphism Presenilin Cerebral disorder Degenerative disease Genetic disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Diagnóstico Demencia Alzheimer Descubrimiento Determinismo genético Gen Hombre Mutación Polimorfismo Presenilina Encéfalo patología Enfermedad degenerativa Enfermedad hereditaria Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1113986
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1212/WNL.57.4.621 
https://dx.doi.org/10.1212/WNL.57.4.621
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