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The Lancet. Neurology|June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association studyDavina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.
Journal of Magnetic Resonance Imaging : JMRI|May 30, 2020
Longitudinal Structural MRI in Neurologically Healthy AdultsSarah Gregory, Keith R Lohse, Eileanoir B Johnson, et al.
Plos Currents|October 13, 2011
NMDA receptor gene variations as modifiers in Huntington disease: a replication studyCarsten Saft, Jörg T Epplen, Stefan Wieczorek, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 4, 2009
The progression of regional atrophy in premanifest and early Huntington's disease: a longitudinal voxel-based morphometry studyNicola Z Hobbs, Susie M D Henley, Gerard R Ridgway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological descriptionMarianne J U Novak, Mary G Sweeney, Abi Li, et al.
Journal of the Neurological Sciences|August 20, 2016
Loss of extra-striatal phosphodiesterase 10A expression in early premanifest Huntington's disease gene carriersHeather Wilson, Flavia Niccolini, Salman Haider, et al.
Human Molecular Genetics|March 16, 2007
Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activationAlexandra Zourlidou, Tali Gidalevitz, Mark Kristiansen, et al.
Journal of Neurology|March 7, 2009
Relationship between CAG repeat length and brain volume in premanifest and early Huntington's diseaseSusie M D Henley, Edward J Wild, Nicola Z Hobbs, et al.
Plos Currents|June 21, 2011
Stability of white matter changes related to Huntington's disease in the presence of imaging noise: a DTI studyHans-Peter Müller, Volkmar Glauche, Marianne J U Novak, et al.
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