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Biomed Research International|September 9, 2014
Mutations in the ATP13A2 gene and Parkinsonism: a preliminary reviewXinglong Yang, Yanming Xu
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 21, 2022
[Genetic analysis of a Chinese pedigree affected with Becker muscular dystrophy with myalgia as the main feature]Dan Xie, Hongyan Huang, Yanming Xu
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 14, 2018
[Clinical and genetic analysis of three pedigrees affected with myotonic dystrophy]Hongyan Huang, Xinglong Yang, Yanming Xu
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 14, 2019
Acute cognitive disorder as the initial manifestation of nitrous oxide abusing: a case reportQiuyan Shen, Haitao Lu, Hui Wang, et al.
Frontiers in Neurology|January 28, 2022
Excessive Daytime Sleepiness Is Associated With Non-motor Symptoms of Multiple System Atrophy: A Cross-Sectional Study in ChinaHui Wang, Xiangdong Tang, Junying Zhou, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 7, 2020
Non-motor symptoms are associated with REM sleep behavior disorder in Parkinson's disease: a systematic review and meta-analysisDan Xie, Qiuyan Shen, Junying Zhou, et al.
Annals of Indian Academy of Neurology|July 31, 2019
Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalomyopathy-Like Syndrome with Polymerase-Gamma MutationsHongyan Huang, Xinglong Yang, Ling Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 9, 2024
[Study of a case of Juvenile neuronal ceroid lipofuscinosis due to compound heterozygous variants of PPT1 gene]Dan Zhang, Fang Xu, Yi Bao, et al.
Molecular Genetics & Genomic Medicine|November 26, 2024
Variability in Disease Severity in Siblings With Homozygous Missense Variant of ADSSL1: Clinical Genetic Study and Review of LiteraturesHui Wang, Ting Zhang, Yanming Xu, et al.
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