Showing results (1-10 of 250) with videos related to

Sort By:
Pageof 25
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 14Dong-Hui Chen, Wendy H Raskind, Thomas D Bird
Neuromuscular Disorders : NMD|July 1, 2020
Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variantsMaxwell T Ma, Dong-Hui Chen, Wendy H Raskind, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|April 24, 2021
Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease ProgressionEvan Zahniser, Thomas D Bird, Dong-Hui Chen, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
Muscle & Nerve|December 14, 2017
An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical featuresDong-Hui Chen, Maxwell Ma, Mena Scavina, et al.
Journal of the Neurological Sciences|July 17, 2010
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutationsDong-Hui Chen, Wendy H Raskind, William W Parson, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Movement Disorders Clinical Practice|January 24, 2020
Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5-DyskinesiaDong-Hui Chen, Caitlin S Latimer, Min Spencer, et al.
American Journal of Medical Genetics|May 7, 2002
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32Zoran Brkanac, Magali Fernandez, Mark Matsushita, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Pageof 25