CareLit · DOI-Nachweis · Klinische Neurophysiologie
Voluntary movement execution in Huntington's disease: A combined neurophysiological and morphometric magnetic resonance imaging study
DOI 10.1055/s-2008-1072863
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Autor:innenC Beste, C Konrad, C Saft, J Andrich, R Gold, B Pfleiderer, M Hausmann, M Falkenstein
ZeitschriftKlinische Neurophysiologie
Ausgabe04/2008
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Huntington's disease is an autosomal dominant neurogenetic disorder leading to striatal atrophy. Characteristic for HD are choreatic involuntary movements, but also voluntary movements deteriorate, but the neurophysiological mechanisms are less understood. In this study we investigated voluntary movement execution by means of movement-related potentials (MRPs) in symptomatic HD (HD) and presymptomatic HD (pHD) and h…
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Zitierempfehlung
C Beste, C Konrad, C Saft, J Andrich, R Gold, B Pfleiderer, M Hausmann, M Falkenstein (2008) Voluntary movement execution in Huntington's disease: A combined neurophysiological and morphometric magnetic resonance imaging study. Klinische Neurophysiologie (04). https://doi.org/10.1055/s-2008-1072863
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