Hasil Pencarian - Min-Ting Lin

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  1. 1
    Effect of a Pay-for-Performance Program on Renal Outcomes Among Patients With Early-Stage Chronic Kidney Disease in Taiwan

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

    Diterbitkan 2022-08-01
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  2. 2
    New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients

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

    Diterbitkan 2015-01-01
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  3. 3
    A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency

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

    Diterbitkan 2016-01-01
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  4. 4
    The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3

    The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3 oleh Hao‐Ling Xu, Qiu‐Ni Su, Xian‐Jin Shang, Arif Sikandar, Min‐Ting Lin, Ning Wang, Hong Lin, Shi‐Rui Gan

    Diterbitkan 2019-07-01
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  5. 5
    Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

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

    Diterbitkan 2016-01-01
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  6. 6
    Apoptosis Sensitization by Euphorbia Factor L1 in ABCB1-Mediated Multidrug Resistant K562/ADR Cells

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

    Diterbitkan 2013-10-01
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  7. 7
    High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis

    High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis oleh Guo-rong Xu, Wei Hu, Ling-Ling Zhan, Chong Wang, Liu-Qing Xu, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Qi-Jie Zhang

    Diterbitkan 2018-04-01
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  8. 8
    The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy

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

    Diterbitkan 2023-03-01
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  9. 9
    Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings

    Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings oleh Qi-Fu Guo, Zhi-Xian Ye, Liang-Liang Qiu, Xin Lin, Jia-He Lai, Min-Ting Lin, Zhi-Qiang Wang, Ning Wang, Feng Lin, Jing Ni

    Diterbitkan 2021-03-01
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  10. 10
    Combinational Treatment of Curcumin and Quercetin against Gastric Cancer MGC-803 Cells in Vitro

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

    Diterbitkan 2015-06-01
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  11. 11
    Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

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

    Diterbitkan 2023-11-01
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  12. 12
    Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients

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

    Diterbitkan 2020-04-01
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  13. 13
    A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy

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

    Diterbitkan 2018-01-01
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  14. 14
    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

    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 oleh 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

    Diterbitkan 2019-07-01
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  15. 15
    A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2

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

    Diterbitkan 2021-11-01
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  16. 16
    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification oleh 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

    Diterbitkan 2022-11-01
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