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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Salvato in:
Dettagli Bibliografici
Pubblicato in:Brain Pathol
Autori principali: Rüb, Udo, Seidel, Kay, Vonsattel, Jean Paul, Lange, Herwig W., Eisenmenger, Wolfgang, Götz, Monika, Del Turco, Domenico, Bouzrou, Mohamed, Korf, Horst‐Werner, Heinsen, Helmut
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2015
Soggetti:
Research Articles
Accesso online: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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