Trends in the treatment changes and medication persistence of chronic myeloid leukemia in Taiwan from 1997 to 2007: a longitudinal population database analysis

por Chang, Chao-Sung, Yang, Yi-Hsin, Hsu, Chien-Ning, Lin, Min-Ting
Publicado 2012

Effect of a Pay-for-Performance Program on Renal Outcomes Among Patients With Early-Stage Chronic Kidney Disease in Taiwan

por Lin, Min-Ting, Hsu, Chien-Ning, Lee, Chien-Te, Cheng, Shou-Hsia
Publicado 2021

New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients

por Lin, Feng, Wang, Zhi-Qiang, Lin, Min-Ting, Murong, Shen-Xing, Wang, Ning
Publicado 2015

A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency

por Liu, Xin-Yi, Wang, Zhi-Qiang, Wang, Dan-Ni, Lin, Min-Ting, Wang, Ning
Publicado 2016

Rapid diagnosis of spinal muscular atrophy using High-Resolution Melting Analysis

por Chen, Wan Jin, Dong, Wan Juan, Lin, Xiao Zhen, Lin, Min Ting, Murong, Shen Xing, Wu, Zhi Ying, Wang, Ning
Publicado 2009

The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3

por Xu, Hao‐Ling, Su, Qiu‐Ni, Shang, Xian‐Jin, Sikandar, Arif, Lin, Min‐Ting, Wang, Ning, Lin, Hong, Gan, Shi‐Rui
Publicado 2019

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

por Liu, Xin-Yi, Jin, Ming, Wang, Zhi-Qiang, Wang, Dan-Ni, He, Jun-Jie, Lin, Min-Ting, Fu, Hong-Xia, Wang, Ning
Publicado 2016

Apoptosis Sensitization by Euphorbia Factor L1 in ABCB1-Mediated Multidrug Resistant K562/ADR Cells

por Zhang, Jian-Ye, Lin, Min-Ting, Yi, Tao, Tang, Yi-Na, Fan, Lan-Lan, He, Xi-Cheng, Zhao, Zhong-Zhen, Chen, Hu-Biao
Publicado 2013

High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis

por Xu, Guo-rong, Hu, Wei, Zhan, Ling-Ling, Wang, Chong, Xu, Liu-Qing, Lin, Min-Ting, Chen, Wan-Jin, Wang, Ning, Zhang, Qi-Jie
Publicado 2018

Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings

por Guo, Qi-Fu, Ye, Zhi-Xian, Qiu, Liang-Liang, Lin, Xin, Lai, Jia-He, Lin, Min-Ting, Wang, Zhi-Qiang, Wang, Ning, Lin, Feng
Publicado 2021

The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy

por Lin, Feng, Yang, Kang, Lin, Min‐ting, Zheng, Fu‐ze, Chen, Long, Ding, Yuan‐liang, Ye, Zhi‐xian, Lin, Xin, Wang, Ning, Wang, Zhi‐qiang
Publicado 2023

Combinational Treatment of Curcumin and Quercetin against Gastric Cancer MGC-803 Cells in Vitro

por Zhang, Jian-Ye, Lin, Min-Ting, Zhou, Meng-Jia, Yi, Tao, Tang, Yi-Na, Tang, Si-Li, Yang, Zhi-Jun, Zhao, Zhong-Zhen, Chen, Hu-Biao
Publicado 2015

Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

por Lin, Feng, Yang, Kang, Lin, Xin, Jin, Ming, Chen, Long, Zheng, Fu-ze, Qiu, Liang-liang, Ye, Zhi-xian, Chen, Hai-zhu, Lin, Min-ting, Wang, Ning, Wang, Zhi-qiang
Publicado 2023

A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy

por Lin, Xiao-Dan, He, Jun-Jie, Lin, Feng, Chen, Hai-Zhu, Xu, Liu-Qing, Hu, Wei, Cai, Nai-Qing, Lin, Min-Ting, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Publicado 2018

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

por Chen, Hai-Zhu, Jin, Ming, Cai, Nai-Qing, Lin, Xiao-Dan, Liu, Xin-Yi, Xu, Liu-Qing, Lin, Min-Ting, Lin, Feng, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Publicado 2019

Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients

por Yang, Jin-Shan, Xu, Hao-Ling, Chen, Ping-Ping, Sikandar, Arif, Qian, Mei-Zhen, Lin, Hui-Xia, Lin, Min-Ting, Chen, Wan-Jin, Wang, Ning, Wu, Hua, Gan, Shi-Rui
Publicado 2020

A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2

por Qiu, Liang-Liang, Lin, Xiao-Dan, Xu, Guo-Rong, Wang, Li-Li, Ye, Zhi-Xian, Lin, Feng, Chen, Hai-Zhu, Lin, Min-Ting, Cai, Nai-Qing, Jin, Ming, Xu, Liu-Qing, Hu, Wei, Wang, Ning, Wang, Zhi-Qiang
Publicado 2021

Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice

por Li, Jin-Jing, Lin, Xiang, Tang, Cheng, Lu, Ying-Qian, Hu, Xinde, Zuo, Erwei, Li, He, Ying, Wenqin, Sun, Yidi, Lai, Lu-Lu, Chen, Hai-Zhu, Guo, Xin-Xin, Zhang, Qi-Jie, Wu, Shuang, Zhou, Changyang, Shen, Xiaowen, Wang, Qifang, Lin, Min-Ting, Ma, Li-Xiang, Wang, Ning, Krainer, Adrian R, Shi, Linyu, Yang, Hui, Chen, Wan-Jin
Publicado 2020

Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

por Zhao, Miao, Su, Hui-Zhen, Zeng, Yi-Heng, Sun, Yuan, Guo, Xin-Xin, Li, Yun-Lu, Wang, Chong, Zhao, Zhi-Yuan, Huang, Xue-Jing, Lin, Kai-Jun, Ye, Zi-Ling, Lin, Bi-Wei, Hong, Shunyan, Zheng, Jitan, Liu, Yao-Bin, Yao, Xiang-Ping, Yang, Dehao, Lu, Ying-Qian, Chen, Hai-Zhu, Zuo, Erwei, Yang, Guang, Wang, Hong-Tao, Huang, Chen-Wei, Lin, Xiao-Hong, Cen, Zhidong, Lai, Lu-Lu, Zhang, Yan-Ke, Li, Xi, Lai, Tianmin, Lin, Jingjing, Zuo, Dan-Dan, Lin, Min-Ting, Liou, Chia-Wei, Kong, Qing-Xia, Yan, Chuan-Zhu, Xiong, Zhi-Qi, Wang, Ning, Luo, Wei, Zhao, Cui-Ping, Cheng, Xuewen, Chen, Wan-Jin
Publicado 2022