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机构 日期 题名 作者
臺大學術典藏 2021-05-25T06:35:53Z De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD MING-CHING SHEN; Chen M.; Ma G.-C.; Chang S.-P.; Lin C.-Y.; Lin B.-D.; Hsieh H.-N.
臺大學術典藏 2021-05-25T06:35:51Z Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent MING-CHING SHEN; Chen M.; Chang S.-P.; Lin P.-T.; Hsieh H.-N.; Lin K.-H.
臺大學術典藏 2021-05-25T06:35:50Z Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; Lin S.-W.; MING-CHING SHEN
臺大學術典藏 2021-05-25T06:35:49Z First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene Chou S.-C.; Lin D.-T.; Lin C.-Y.; Huang Y.-C.; Hsieh H.-N.; MING-CHING SHEN
臺大學術典藏 2021-02-01T00:48:43Z Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; KO-JEN LI; Lin S.-W.; Shen M.-C.
臺大學術典藏 2021-01-05T02:30:54Z Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan Shen M.-C.; Lin S.-W.; Li K.-J.; Huang Y.-C.; Hsieh H.-N.; Yen C.-T.; Lin C.-Y.; SHENG-CHIEH CHOU
臺大學術典藏 2020-06-22T07:36:55Z Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan Chou S.-C.;Lin C.-Y.;Yen C.-T.;Hsieh H.-N.;Huang Y.-C.;Li K.-J.;Shu-Wha Lin;Shen M.-C.; Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; SHU-WHA LIN; Shen M.-C.
臺大學術典藏 2018-09-10T15:38:52Z De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD Shen, M.-C.;Chen, M.;Ma, G.-C.;Chang, S.-P.;Lin, C.-Y.;Lin, B.-D.;Hsieh, H.-N.; MING CHEN

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