Showing results (171-180 of 210) with videos related to

Sort By:
Pageof 21
Human Genetics|March 17, 2004
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24Bei-Sha Tang, Wei Luo, Kun Xia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2024
Potential Disease-Modifying Effects of Ganglioside GM1 Pulse Treatment on Spinocerebellar Ataxia Type 3, a Parallel-Group, Double-Blind, Randomized, Controlled TrialYong-Kang Chen, Hai-Yan Tian, Qing-Yong Zhu, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 10, 2013
Distribution of transglutaminase 6 in the central nervous system of adult miceYu-Tao Liu, Bei-Sha Tang, Wei Lan, et al.
Neuroscience Letters|July 31, 2013
Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseasesJun-Ling Wang, Xiao Mao, Zheng-Mao Hu, et al.
Frontiers in Neuroanatomy|June 23, 2017
Sortilin Fragments Deposit at Senile Plaques in Human CerebrumXia Hu, Zhao-Lan Hu, Zheng Li, et al.
Human Genetics|November 27, 2004
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2LBei-sha Tang, Guo-hua Zhao, Wei Luo, et al.
The Journal of Clinical Endocrinology and Metabolism|May 4, 2013
Two novel functional single nucleotide polymorphisms of ADRB3 are associated with type 2 diabetes in the Chinese populationQiong Huang, Tian-Lun Yang, Bei-Sha Tang, et al.
Plos One|September 3, 2014
Genetic diagnosis of two dopa-responsive dystonia families by exome sequencingZhan-fang Sun, Yu-han Zhang, Ji-feng Guo, et al.
Neurology. Genetics|April 29, 2016
Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 geneXiao-Rong Liu, Dan Huang, Jie Wang, et al.
Neuroscience Letters|February 25, 2010
Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese populationLei Wang, Ji-feng Guo, Wen-wen Zhang, et al.
Pageof 21