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Current Neurology and Neuroscience Reports|June 23, 2014
Recent advances in the genetics of dystoniaJianfeng Xiao, Satya R Vemula, Mark S LeDouxJournal of the Neurological Sciences|March 6, 2016
Blepharospasm in a multiplex African-American pedigreeJianfeng Xiao, Misty M Thompson, Satya R Vemula, et al.Neurology|March 7, 2014
Pathogenic variants in TUBB4A are not found in primary dystoniaSatya R Vemula, Jianfeng Xiao, Robert W Bastian, et al.BMC Medical Genetics|July 16, 2013
Dystonia, facial dysmorphism, intellectual disability and breast cancer associated with a chromosome 13q34 duplication and overexpression of TFDP1: case reportMariana Moscovich, Mark S LeDoux, Jianfeng Xiao, et al.Human Molecular Genetics|March 2, 2013
Role of Gα(olf) in familial and sporadic adult-onset primary dystoniaSatya R Vemula, Andreas Puschmann, Jianfeng Xiao, et al.Experimental Neurology|May 11, 2016
Motor phenotypes and molecular networks associated with germline deficiency of Ciz1Jianfeng Xiao, Satya R Vemula, Yi Xue, et al.Parkinsonism & Related Disorders|March 2, 2012
Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new casesMark S LeDoux, Jianfeng Xiao, Monika Rudzińska, et al.Neurobiology of Disease|November 29, 2016
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndromeJianfeng Xiao, Satya R Vemula, Yi Xue, et al.Annals of Neurology|March 27, 2012
Mutations in CIZ1 cause adult onset primary cervical dystoniaJianfeng Xiao, Ryan J Uitti, Yu Zhao, et al.Molecular Genetics & Genomic Medicine|May 18, 2018
Whole-exome sequencing for variant discovery in blepharospasmJun Tian, Satya R Vemula, Jianfeng Xiao, et al.Pageof 2