The importance of early diagnosis and treatment in treatable neuromuscular diseases

by Cheng ZHANG, Yu-ling ZHU
Published 2018-08-01

Analysis on clinical phenotype and gene mutation of two cases of limb - girdle muscular dystrophy type 2A during preclinical stage

by Huan LI, Yu-ling ZHU, Jing LI, Liang WANG, Ruo-jie HE, Jin-fu LIN, Cheng ZHANG
Published 2018-07-01

Analysis of clinical phenotype and genetic mutation with outcome evaluation in one family of vitamin B12-dependent methylmalonic aciduria

by LI Jing, Yi-ming SUN, Li-yu OU, Yu-ling ZHU, Liang WANG, Huan LI, Cheng ZHANG
Published 2017-07-01

Treatment of Becker myotonia congenita with lamotrigine: one case report and review of literatures

by Jie ZHONG, Jin-fu LIN, Cheng ZHANG, Xin-jing ZHONG, Xue-ling CHEN, Jing LI, Yu-ling ZHU
Published 2019-05-01

Correlation analysis between genotype and phenotype of patients with facioscapulohumeral muscular dystrophy type 1

by Huan LI, Qiu CHEN, Jin-fu LIN, Zi-yu LIAO, Liang WANG, Jing LI, Yu-ling ZHU, Cheng ZHANG
Published 2019-05-01

A novel mutation in GNE gene: clinical characteristics and bioinformatics analysis

by Liang WANG, Ya-qin LI, Hui-li ZHANG, Yu-ling ZHU, Ruo-jie HE, Huan LI, Jin-fu LIN, Cheng ZHANG
Published 2018-08-01

Clinical characteristics and MTMR13/SBF2 gene mutation analysis of a Charcot - Marie-Tooth disease type 4B2 Chinese family

by Yu-ling ZHU, Huan LI, Zhi-liang PAN, Ying-yin LIANG, Jing LI, Ruo-jie HE, Jin-fu LIN, Cheng ZHANG
Published 2018-08-01

Study on skeletal muscle dystrophin and neuromuscular junction in adult and young mdx mice

by Yu-ling ZHU, Yi-ming SUN, Hui-li ZHANG, Yu ZHANG, Ya-qin LI, Meng-long CHEN, Liang WANG, Cheng ZHANG
Published 2015-05-01

Analysis on clinical phenotype and gene mutation of three cases of dysferlinopathy in two families

by Hui-li ZHANG, Ze LI, Qiu-sheng CHENG, Xi CHEN, Yu-ling ZHU, Ya-qin LI, Meng-long CHEN, Cheng ZHANG
Published 2018-07-01

Clinical phenotype and genotype analysis on a family of Becker muscular dystrophy caused by a novel missense mutation of DMD gene

by Yun-qing GAO, Li-yu OU, Ya-qin LI, Jing LI, Jin-fu LIN, Ruo-jie HE, Huan LI, Yu-ling ZHU, Cheng ZHANG
Published 2019-05-01

Genetic analysis and clinical features of familial hypokalemic periodic paralysis

by Hui-li ZHANG, Yi-ming SUN, Min-ying ZHENG, Yu-ling ZHU, Ji-qing CAO, Yu ZHANG, Ya-qin LI, Lang-hui DENG, Cheng ZHANG
Published 2014-06-01

Adipose-derived stem cells enhance myogenic differentiation in the mdx mouse model of muscular dystrophy via paracrine signaling

by Ji-qing Cao, Ying-yin Liang, Ya-qin Li, Hui-li Zhang, Yu-ling Zhu, Jia Geng, Li-qing Yang, Shan-wei Feng, Juan Yang, Jie Kong, Cheng Zhang
Published 2016-01-01

Study on preimplantation genetic diagnosis and follow-up for Duchenne muscular dystrophy

by Juan YANG, Hui-fang XIE, Ji-qing CAO, Hui ZHENG, Can-quan ZHOU, Zhen-hua LIU, Yu-ling ZHU, Yi-xin ZHAN, Xiao-ting SHEN, Ya-qin LI, Cheng ZHANG
Published 2015-06-01

Clinical study of DMD gene point mutation causing Becker muscular dystrophy

by Ji-qing CAO, Juan YANG, Ya-qin LI, Shan-wei FENG, Fei CHEN, Hui ZHENG, Ying-yin LIANG, Bao-jian ZHAO, Xu ZHANG, Hui-li ZHANG, Yu-ling ZHU, Cheng ZHANG
Published 2015-06-01

Clinical characteristics and gene mutation analysis of riboflavin-responsive lipid storage myopathy: report of 3 cases in 2 families and review of literature

by Ji-qing CAO, Cheng ZHANG, Ya-qin LI, Juan YANG, Ying-yin LIANG, Shan-wei FENG, Xu ZHANG, Jing LI, Hui-li ZHANG, Yu-ling ZHU, Jia GENG, Li-qing YANG
Published 2014-06-01