Research progress of electrophysiology for the diagnosis of metabolic myopathyZHAO Lei, CUI Li-ying468-470
Clinical characteristics and gene mutation analysis of riboflavin-responsive lipid storage myopathy: report of 3 cases in 2 families and review of literature操基清, 张成, 李亚勤, 杨娟, 梁颖茵, 冯善伟, 张旭, 利婧, 张惠丽479-484
Comparison of muscle pathology in riboflavin-responsive lipid storage myopathy before and after treatment: one case report and review of literature陈定邦, 吴超, 冯黎, 莫桂玲, 廖冰, 刘大伟, 吴金浪, 吴强, 李洵桦485-489
Genetic analysis and clinical features of familial hypokalemic periodic paralysis张惠丽, 孙毅明, 郑民缨, 朱瑜龄, 操基清, 张誉, 李亚勤, 邓琅辉, 张成490-495
Clinical pathological and genetic analysis of 2 cases of mitochondrial myopathy presented as acute motor axonal neuropathyYIN Hou-min, SHAO Yu-quan, LIU Li, SHEN Chun-hong, DU Ai-lian496-501
Anatomic research of suboccipito-retrosigmoidal approach for minimally invasive exposure of facial-acoustic nerve complex utilizing virtual reality skillTANG Ke, ZHOU Jing-an, ZHOU Qing, ZHAO Ya-qun, LIU Ce502-506
Brain protective effect of dexmedetomidine on perioperative patients in temporal muscle sticking for moyamoya diseaseCHEN Jun, ZHOU Qiang, LIANG Yu507-511
Aggravation of spatial learning and memory impairment by type 2 diabetes mellitus in rats with chronic cerebral hypoperfusion and its possible mechanismLI Yu-mei, LIU Yu, ZHANG Ting, FU Jian-liang512-517