Spinocerebellar ataxia type 8 in Scotland : frequency, neurological, neuropsychological and neuropsychiatric findings
- Author
- TORRENS, L1 ; BURNS, E2 ; STONE, J3 ; GRAHAM, C4 ; WRIGHT, H1 ; SUMMERS, D3 ; SELLAR, R3 ; PORTEOUS, M5 ; WARNER, J5 ; ZEMAN, A6
[1] The Robert Fergusson Unit, Royal Edinburgh Hospital, Edinburgh, United Kingdom
[2] Medical School, Western General Hospital, University of Edinburgh, Edinburgh, United Kingdom
[3] Department of Clinical Neurosciences, Western General Hospital, Edinburgh, United Kingdom
[4] Wellcome Trust Clinical Research Facility, Western General Hospital, Edinburgh, United Kingdom
[5] Department of Clinical Genetics, Western General Hospital, Edinburgh, United Kingdom
[6] Department of Neurology, Peninsula Medical School, Exeter, United Kingdom - Source
Acta neurologica scandinavica. 2008, Vol 117, Num 1, pp 41-48, 8 p ; ref : 30 ref
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- higher cortical functions neurodegenerative disorders neuropsychology spinocerebellar atrophy
- Keyword (fr)
- Ataxie spinocérébelleuse Atrophie Pathologie du système nerveux Maladie dégénérative Maladie héréditaire Pathologie du système nerveux central
- Keyword (en)
- Spinocerebellar ataxia Atrophy Nervous system diseases Degenerative disease Genetic disease Central nervous system disease
- Keyword (es)
- Ataxia spinocerebelosa Atrofia Sistema nervioso patología Enfermedad degenerativa Enfermedad hereditaria 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 / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D03 Carbohydrates (enzymatic deficiencies). Glycogenosis
- Discipline
- Metabolic diseases Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19985051
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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