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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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Podrobná bibliografie
Vydáno v:Brain Pathol
Hlavní autoři: Rüb, Udo, Seidel, Kay, Vonsattel, Jean Paul, Lange, Herwig W., Eisenmenger, Wolfgang, Götz, Monika, Del Turco, Domenico, Bouzrou, Mohamed, Korf, Horst‐Werner, Heinsen, Helmut
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
On-line přístup: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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