The progress in diagnosis and treatment of transthyretin amyloid polyneuropathyZHU Xi-ying, LIU Lei, ZHANG Ru-xu430-438
Application of muscle MRI in diagnosis of hereditary myopathiesSONG Jia, PANG Mi, LI Gang, FU Jun, MA Ming-ming439-447
Advances in quantitative MRI of hereditary myopathiesLIANG Ying-yin, LI Gui-dian, HE Rong-xing, WANG Liang, ZHANG Cheng448-453
Clinical characteristics and therapeutic evaluation of autosomal recessive juvenil-onset Parkinson's diseaseZHANG Yue, ZHANG Cheng, LI Juan, WU Jing-jing, LIN Dong454-459
Clinical symptoms and molecular biology research in a family with oculopharyngeal muscular dystrophyHUANG Kai, LI Wen-wu, LIU Hong-xian, SUN Hao, LI Zhi-hong, CHU Jia-you, YANG Zhao-qing460-465
Clinical,muscle pathology and molecular biological features of late-onset glycogen storage disease type ⅡWU Shi-tao, LIU Fang, SHI Wei-wei, ZHANG Min, LIU Heng-fang466-472
Familial amyotrophic lateral sclerosis with FUS gene mutation:one case reportLI Xiang, ZHANG Hui-yuan, ZHANG Jian, HE Zhi-yi473-477
Clinical and imaging features of a pedigree with spinocerebellar ataxia type 6YANG Yun-peng, LIU Jia, WANG Lu-ning478-481
Early-onset Parkinson's disease with PARK2 gene mutation:one case reportLI Mao-lin, ZENG Tao, FENG Qin, WANG Chun482-484
