Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

BACKGROUND: Cerebellar atrophy is a nonspecific imaging finding observed in a number of neurological disorders. Genetic ataxias associated with cerebellar atrophy are a heterogeneous group of conditions, rendering the approach to diagnosis challenging. OBJECTIVES: To define the spectrum of genetic a...

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Detalhes bibliográficos
Publicado no:Mov Disord Clin Pract
Main Authors: Gauquelin, Laurence, Hartley, Taila, Tarnopolsky, Mark, Dyment, David A., Brais, Bernard, Geraghty, Michael T., Tétreault, Martine, Ahmed, Sohnee, Rojas, Samantha, Choquet, Karine, Majewski, Jacek, Bernier, François, Innes, Allan Micheil, Rouleau, Guy, Suchowersky, Oksana, Boycott, Kym M., Yoon, Grace
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2020
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Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7604675/
https://ncbi.nlm.nih.gov/pubmed/33163565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.13086
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