Works by Lin, Shuan-Pei


Results: 131
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    Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome.

    Published in:
    Journal of Personalized Medicine, 2021, v. 11, n. 11, p. 1197, doi. 10.3390/jpm11111197
    By:
    • Lin, Hsiang-Yu;
    • Lee, Chung-Lin;
    • Fran, Sisca;
    • Tu, Ru-Yi;
    • Chang, Ya-Hui;
    • Niu, Dau-Ming;
    • Chang, Chia-Ying;
    • Chiu, Pao-Chin;
    • Chou, Yen-Yin;
    • Hsiao, Hui-Pin;
    • Tsai, Meng-Che;
    • Chao, Mei-Chyn;
    • Tsai, Li-Ping;
    • Yang, Chia-Feng;
    • Su, Pen-Hua;
    • Pan, Yu-Wen;
    • Lee, Chen-Hao;
    • Chu, Tzu-Hung;
    • Chuang, Chih-Kuang;
    • Lin, Shuan-Pei
    Publication type:
    Article
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    Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese.

    Published in:
    NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0091-x
    By:
    • Yu, Mullin Ho-Chung;
    • Tsang, Mandy Ho-Yin;
    • Lai, Sophie;
    • Ho, Matthew Sai-Pong;
    • Tse, Donald M. L.;
    • Willis, Brooke;
    • Kwong, Anna Ka-Yee;
    • Chou, Yen-Yin;
    • Lin, Shuan-Pei;
    • Quinzii, Catarina M;
    • Hwu, Wuh-Liang;
    • Chien, Yin-Hsiu;
    • Kuo, Pao-Lin;
    • Chan, Victor Chi-Man;
    • Tsoi, Cheung;
    • Chong, Shuk-Ching;
    • Rodenburg, Richard J. T.;
    • Smeitink, Jan;
    • Mak, Christopher Chun-Yu;
    • Yeung, Kit-San
    Publication type:
    Article
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    Omphalocele and Gastroschisis in Taiwan.

    Published in:
    European Journal of Pediatrics, 2002, v. 161, n. 10, p. 552, doi. 10.1007/s00431-002-1031-8
    By:
    • Hsu, Chia-Chi;
    • Lin, Shuan-Pei;
    • Chen, Chao-Huei;
    • Chi, Ching-Shiang;
    • Lee, Hung-Chang;
    • Hung, Han-Yang;
    • Kao, Hsin-An;
    • Hsu, Chyon-Hsin
    Publication type:
    Article
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    Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study.

    Published in:
    Journal of Inherited Metabolic Disease, 2014, v. 37, n. 6, p. 979, doi. 10.1007/s10545-014-9715-6
    By:
    • Hendriksz, Christian;
    • Burton, Barbara;
    • Fleming, Thomas;
    • Harmatz, Paul;
    • Hughes, Derralynn;
    • Jones, Simon;
    • Lin, Shuan-Pei;
    • Mengel, Eugen;
    • Scarpa, Maurizio;
    • Valayannopoulos, Vassili;
    • Giugliani, Roberto;
    • Slasor, Peter;
    • Lounsbury, Debra;
    • Dummer, Wolfgang
    Publication type:
    Article
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    Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan.

    Published in:
    Journal of Inherited Metabolic Disease, 2010, v. 33, p. 421, doi. 10.1007/s10545-010-9212-5
    By:
    • Lin, Hsiang‐Yu;
    • Chen, Ming‐Ren;
    • Chuang, Chih‐Kuang;
    • Chen, Chih‐Ping;
    • Lin, Dar‐Shong;
    • Chien, Yin‐Hsiu;
    • Ke, Yu‐Yuan;
    • Tsai, Fuu‐Jen;
    • Pan, Hui‐Ping;
    • Lin, Shio‐Jean;
    • Hwu, Wuh‐Liang;
    • Niu, Dau‐Ming;
    • Lee, Ni‐Chung;
    • Lin, Shuan‐Pei
    Publication type:
    Article
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    Prenatal diagnosis of X-linked myotubular myopathy.

    Published in:
    Prenatal Diagnosis, 2010, v. 30, n. 2, p. 177, doi. 10.1002/pd.2432
    By:
    • Chen, Chih-Ping;
    • Lin, Shuan-Pei;
    • Chern, Schu-Rern;
    • Tsai, Fuu-Jen;
    • Wang, Tao-Yeuan;
    • Lin, Hung-Hung;
    • Wang, Wayseen
    Publication type:
    Article
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