Showing results (31-40 of 100) with videos related to
Sort By:
Pageof 10
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 1, 2010
Biomarkers of disease in a case of familial lower motor neuron ALSFusun Baumann, Stephen E Rose, Garth A Nicholson, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 20, 2012
A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosisJennifer A Solski, Shu Yang, Garth A Nicholson, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 2013
Pathophysiological insights into ALS with C9ORF72 expansionsKelly L Williams, Jennifer A Fifita, Steve Vucic, et al.Neurobiology of Aging|December 20, 2014
Mutation analysis of MATR3 in Australian familial amyotrophic lateral sclerosisJennifer A Fifita, Kelly L Williams, Emily P McCann, et al.JAMA Neurology|September 9, 2015
Cortical Function in Asymptomatic Carriers and Patients With C9orf72 Amyotrophic Lateral SclerosisNimeshan Geevasinga, Parvathi Menon, Garth A Nicholson, et al.Neurobiology of Aging|June 22, 2012
UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosisKelly L Williams, Sadaf T Warraich, Shu Yang, et al.Neurotoxicity Research|May 28, 2015
Evaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological FeaturesShu Yang, Katharine Y Zhang, Ruvini Kariawasam, et al.Journal of Neuropathology and Experimental Neurology|October 30, 2008
Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutationsJean-Michel Vallat, Robert A Ouvrier, John D Pollard, et al.Molecular Genetics & Genomic Medicine|March 25, 2015
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencingAlexander P Drew, Danqing Zhu, Aditi Kidambi, et al.Neurology|February 1, 2013
DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing lossChristopher J Klein, Tom Bird, Nilufer Ertekin-Taner, et al.Pageof 10