EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.

Gasser, T; Finsterer, J; Baets, J; Van Broeckhoven, C; Di Donato, S; Fontaine, B; De Jonghe, P; Lossos, A; Lynch, T; Mariotti, C; Schöls, L; Spinazzola, A; Szolnoki, Z; Tabrizi, S J; Tallaksen, C M E; Zeviani, M; Burgunder, J-M; Harbo, H F

Gasser, T; Finsterer, J; Baets, J; Van Broeckhoven, C; Di Donato, S; Fontaine, B; De Jonghe, P; Lossos, A; Lynch, T; Mariotti, C; Schöls, L; Spinazzola, A; Szolnoki, Z; Tabrizi, S J; Tallaksen, C M E; Zeviani, M; Burgunder, J-M; Harbo, H F.

Affiliation

Gasser T; Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany. thomas.gasser@uni-tuebingen.de

Eur J Neurol ; 17(2): 179-88, 2010 Feb.

Article in En | MEDLINE | ID: mdl-20050888

Subject(s)

Ataxia/diagnosis; Ataxia/genetics; Spastic Paraplegia, Hereditary/diagnosis; Spastic Paraplegia, Hereditary/genetics; Ataxia/metabolism; Humans; Paraplegia/diagnosis; Paraplegia/genetics; Paraplegia/metabolism; Spastic Paraplegia, Hereditary/metabolism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / Spastic Paraplegia, Hereditary Type of study: Diagnostic_studies / Guideline Limits: Humans Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2010 Type: Article Affiliation country: Germany

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