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The Journal of Comparative Neurology|October 2, 2002
Human GABA A receptors on dopaminergic neurons in the pars compacta of the substantia nigraSusanne Petri, Klaus Krampfl, Reinhard Dengler, et al.Journal of the Neurological Sciences|September 28, 2005
Executive dysfunction in early stages of Huntington's disease is associated with striatal and insular atrophy: a neuropsychological and voxel-based morphometric studyAlexander Peinemann, Sabine Schuller, Córina Pohl, et al.Neuroreport|April 13, 2004
Global cerebral atrophy in early stages of Huntington's disease: quantitative MRI studyJan Kassubek, G Bernhard Landwehrmeyer, Daniel Ecker, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 31, 2007
Striatal gray matter loss in Huntington's disease is leftward biasedMark Mühlau, Christian Gaser, Afra M Wohlschläger, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 21, 2010
Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's diseaseRalf Reilmann, Stefan Bohlen, Thomas Klopstock, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Grasping premanifest Huntington's disease - shaping new endpoints for new trialsRalf Reilmann, Stefan Bohlen, Thomas Klopstock, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 18, 2010
GABAergic dysfunction in essential tremor: an 11C-flumazenil PET studyHenning Boecker, Adolf Weindl, David J Brooks, et al.Journal of Neurology|January 27, 2005
Creatine supplementation lowers brain glutamate levels in Huntington's diseaseAndreas Bender, Dorothee P Auer, Thomas Merl, et al.Annals of Neurology|January 27, 2006
Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulationMonika B Hartig, Konstanze Hörtnagel, Barbara Garavaglia, et al.Pageof 1