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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

ISSN
0885-3185
Scientific domain
Neurology
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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