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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.
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
ABSTRACT
BACKGROUND AND

PURPOSE:

These EFNS guidelines on the molecular diagnosis of neurogenetic disorders are designed to provide practical help for the general neurologist to make appropriate use of molecular genetics in diagnosing neurogenetic disorders.

METHODS:

Literature searches were performed before expert members of the task force wrote proposals, which were discussed in detail until final consensus had been reached among all task force members. RESULTS AND

CONCLUSION:

This paper provides updated guidelines for molecular diagnosis of two particularly complex groups of disorders, the ataxias and spastic paraplegias. Possibilities and limitations of molecular genetic diagnosis of these disorders are evaluated and recommendations are provided.
Subject(s)

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

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