Analysis of the glucocerebrosidase gene in Parkinson's disease
- Author
- SATO, Christine1 ; MORGAN, Angharad1 ; LANG, Anthony E2 ; SALEHI-RAD, Shabnam1 ; KAWARAI, Toshitaka1 ; YAN MENG3 ; RAY, Peter N4 ; FARRER, Lindsay A3 ; ST GEORGE-HYSLOP, Peter1 5 ; ROGAEVA, Ekaterina1 6
[1] Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada
[2] Movement Disorders Centre, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada
[3] Boston University, School of Medicine, Boston, Massachusetts, United States
[4] Departments of Genetics and Pediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada
[5] Department of Medicine, Division of Neurology, University Health Network, Toronto, Ontario, Canada
[6] Department of Medicine, Division of Neurology, University of Toronto, Toronto, Ontario, Canada - Source
Movement disorders. 2004, Vol 20, Num 3, pp 367-370, 4 p ; ref : 20 ref
- Publisher
- Wiley, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- Gaucher's disease Parkinson's disease glucocerebrosidase risk factors
- Keyword (fr)
- Facteur risque Lipide Parkinson maladie Sphingolipidose héréditaire Gaucher Système nerveux pathologie Encéphale pathologie Enzymopathie Extrapyramidal syndrome Lipoïdose Maladie dégénérative Maladie héréditaire Métabolisme pathologie Système nerveux central pathologie
- Keyword (en)
- Risk factor Lipids Parkinson disease Gaucher disease Nervous system diseases Cerebral disorder Enzymopathy Extrapyramidal syndrome Lipoidosis Degenerative disease Genetic disease Metabolic diseases Central nervous system disease
- Keyword (es)
- Factor riesgo Lípido Parkinson enfermedad Esfingolipidosis hereditaria Gaucher Sistema nervioso patología Encéfalo patología Enzimopatía Extrapiramidal síndrome Lipoidosis Enfermedad degenerativa Enfermedad hereditaria Metabolismo patología Sistema nervosio central patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A03 Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
- 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
- 16714079
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
10.1002/mds.20319 
https://dx.doi.org/10.1002/mds.20319
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