The clinical and genetical heterogeneity of riboflavin ⁃ responsive multiple acyl ⁃ coenzyme A dehydrogenase deficiency por Yi-ming SUN, Ji-qing CAO, Jing LI, Huan LI, Cheng ZHANG

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Study on T2 mapping in thigh muscles of patients with Duchenne muscular dystrophy por Ying-yin LIANG, Ji-qing CAO, Jian LING, Er-jian LIN, Ming LI, Cheng ZHANG

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Genetic analysis and clinical features of familial hypokalemic periodic paralysis por 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

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

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Clinical features and genetic analysis of tuberous sclerosis pedigrees por Ya⁃qin LI, Ji⁃qing CAO, Juan YANG, Bao⁃feng ZHANG, Shan⁃wei FENG, Yan⁃yun WANG, Yao ZHANG, Fei CHEN, Jie KONG, Min⁃ying ZHENG, Xu ZHANG, Cheng ZHANG

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Clinical efficacy of Myozyme on one ventilator dependent patient with late-onset glycogen storage disease typeⅡ por Juan YANG, Wei-xun FENG, Ji-qing CAO, Yan-yun WANG, Ya-qin LI, Shi-biao HUANG, Yan-jun LUO, Zhuo-lin LIU, Yi-ming SUN, Zhen-hua LIU, Cheng ZHANG

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Clinical study of DMD gene point mutation causing Becker muscular dystrophy por 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

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

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