Clinical and mechanism research progress on short tandem repeat-related neuromuscular diseasesWAN Ya-lan, YU Jia-xi, DENG Jian-wen, HONG Dao-jun, WANG Zhao-xia775-781
Analysis of clinical and histopathology characteristics of asymptomatic and pauci-symptomatic hyperCKemiaYUAN Yu-jing, LIU Chang, XIE Zhi-ying, ZHAO Ya-wen, MENG Ling-chao, LÜ He, WANG Zhao-xia, YUAN Yun, ZHANG Wei782-788
Analysis of clinical and pathological characteristics of scleromyositis patients with positive anti-Ku or anti-PM-Scl antibodiesZHANG Xin-yu, ZHAO Ya-wen, ZHANG Wei, WANG Zhao-xia, YUAN Yun789-797
Oculopharyngodistal myopathy caused by CGG repeat expansion in 5'untranslated region of LRP12 gene:four cases reportYU Jia-xi, YU Meng, ZHANG Wei, YUAN Yun, DENG Jian-wen, WANG Zhao-xia798-806
Analysis of clinical and electrophysiological charactertics of hereditary neuropathy with liability to pressure palsiesLI Yi, JIANG Yun, HE Jing, YU Hui-yan, WANG Xiang, LIU Yin-hong807-812
Hereditary myopathy with early respiratory failure in China:one case report and literatures reviewLI Ying, QI Xue-liang, ZHANG Wei, FENG Li-qun, LIU Guang-zhi, YUAN Yun813-820
Mitochondrial myopathy presenting as acute respiratory failure:one case reportWANG Hui, YU Meng, LÜ He, ZHANG Wei, YUAN Yun, WANG Zhao-xia821-825
Phosphoserine aminotransferase deficiency in childhood ichthyosis with adolescent peripheral neuropathy caused by PSAT1 gene mutation:one case reportLI Ping, XU Yan-fang, HU Shuai, ZENG Xiao-xia, QI Xue-liang826-831
Limb-girdle muscular dystrophy with congenital myasthenic syndrome caused by GMPPB gene mutation:one case reportLI Ran, ZOU Hui-min, XING Chun-ye, SONG Jin, HAO Yan-lei832-837