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Huntington's Disease (HD): Neurodegeneration of Brodmann's Primary Visual Area 17 (BA17)

Huntington's disease (HD), an autosomal dominantly inherited polyglutamine or CAG repeat disease along with somatomotor, oculomotor, psychiatric and cognitive symptoms, presents clinically with impairments of elementary and complex visual functions as well as altered visual‐evoked potentials (V...

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Detalles Bibliográficos
Publicado en:Brain Pathol
Main Authors: Rüb, Udo, Seidel, Kay, Vonsattel, Jean Paul, Lange, Herwig W., Eisenmenger, Wolfgang, Götz, Monika, Del Turco, Domenico, Bouzrou, Mohamed, Korf, Horst‐Werner, Heinsen, Helmut
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2015
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8029049/
https://ncbi.nlm.nih.gov/pubmed/25495445
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12237
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