Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2

OBJECTIVE: Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited neurodegenerative disease mainly affecting the cerebellum and brainstem. In this Cuban‐German research collaboration, we aimed to characterize atrophy patterns and associations with clinical measures in preclinical...

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Vydáno v:Ann Clin Transl Neurol
Hlavní autoři: Reetz, Kathrin, Rodríguez‐Labrada, Roberto, Dogan, Imis, Mirzazade, Shahram, Romanzetti, Sandro, Schulz, Jörg B., Cruz‐Rivas, Edilia M., Alvarez‐Cuesta, Jose A., Aguilera Rodríguez, Raul, Gonzalez Zaldivar, Yanetza, Auburger, Georg, Velázquez‐Pérez, Luis
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2018
Témata:
Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5817824/
https://ncbi.nlm.nih.gov/pubmed/29468174
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.504
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