Effect of a Pay-for-Performance Program on Renal Outcomes Among Patients With Early-Stage Chronic Kidney Disease in Taiwan by Min-Ting Lin, Chien-Ning Hsu, Chien-Te Lee, Shou-Hsia Cheng

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New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients by Feng Lin, Zhi-Qiang Wang, Min-Ting Lin, Shen-Xing Murong, Ning Wang

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A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency by Xin-Yi Liu, Zhi-Qiang Wang, Dan-Ni Wang, Min-Ting Lin, Ning Wang

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Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations by Xin-Yi Liu, Ming Jin, Zhi-Qiang Wang, Dan-Ni Wang, Jun-Jie He, Min-Ting Lin, Hong-Xia Fu, Ning Wang

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Apoptosis Sensitization by Euphorbia Factor L1 in ABCB1-Mediated Multidrug Resistant K562/ADR Cells by Zhong-Zhen Zhao, Hu-Biao Chen, Lan-Lan Fan, Xi-Cheng He, Yi-Na Tang, Tao Yi, Jian-Ye Zhang, Min-Ting Lin

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The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy by Feng Lin, Kang Yang, Min‐ting Lin, Fu‐ze Zheng, Long Chen, Yuan‐liang Ding, Zhi‐xian Ye, Xin Lin, Ning Wang, Zhi‐qiang Wang

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Combinational Treatment of Curcumin and Quercetin against Gastric Cancer MGC-803 Cells in Vitro by Jian-Ye Zhang, Min-Ting Lin, Meng-Jia Zhou, Tao Yi, Yi-Na Tang, Si-Li Tang, Zhi-Jun Yang, Zhong-Zhen Zhao, Hu-Biao Chen

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Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients by Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang

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Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients by Jin-Shan Yang, Hao-Ling Xu, Ping-Ping Chen, Arif Sikandar, Mei-Zhen Qian, Hui-Xia Lin, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Hua Wu, Shi-Rui Gan

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A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy by Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu

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Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency by Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui

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A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2 by Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo

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Loss of function of CMPK2 causes mitochondria deficiency and brain calcification by Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen

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