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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...

詳細記述

保存先:
書誌詳細
出版年:Brain Pathol
主要な著者: Rüb, Udo, Seidel, Kay, Vonsattel, Jean Paul, Lange, Herwig W., Eisenmenger, Wolfgang, Götz, Monika, Del Turco, Domenico, Bouzrou, Mohamed, Korf, Horst‐Werner, Heinsen, Helmut
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2015
主題:
オンライン・アクセス: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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