臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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	造訪人次 : 50983332 線上人數 : 911 教育部委託研究計畫計畫執行:國立臺灣大學圖書館

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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機構	日期	題名	作者
臺大學術典藏	2021-05-25T06:35:53Z	Characteristics of Taiwanese patients of PNH in the international PNH registry	Chou W.-C.; Huang W.-H.; Wang M.-C.; Chang C.-S.; Yeh S.-P.; Chiou T.-J.; Chen Y.-C.; Lin T.-H.; MING-CHING SHEN; on behalf of the Taiwan PNH study group
臺大學術典藏	2021-05-25T06:35:52Z	Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: A historical control cohort study from Taiwan	MING-CHING SHEN; Wu W.-J.; Cheng P.-J.; Ma G.-C.; Li W.-C.; Liou J.-D.; Chang C.-S.; Lin W.-H.; Chen M.
臺大學術典藏	2021-05-25T06:35:52Z	No best, only better: Another APSTH milestone	MING-CHING SHEN
臺大學術典藏	2021-05-25T06:35:51Z	Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations	Lin H.-Y.;Lin C.-Y.;Hung M.-H.;Kuo S.-F.;Lin J.-S.;Ming-Ching Shen; Lin H.-Y.; Lin C.-Y.; Hung M.-H.; Kuo S.-F.; Lin J.-S.; MING-CHING SHEN
臺大學術典藏	2021-05-25T06:35:51Z	A systematic review evaluating the efficacy and factor consumption of long-acting recombinant factor VIII products for the prophylactic treatment of hemophilia A	Graf L.;Yan S.;Ming-Ching Shen;Balasa V.; Graf L.; Yan S.; MING-CHING SHEN; Balasa V.
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	2021-05-25T06:35:51Z	Transfusion-transmitted infection and comorbidities in patients with severe haemophilia: A longitudinal birth cohort analysis	Wang J.-D.;Lin C.-Y.;Weng T.-F.;Chiou S.-S.;Peng C.-T.;Ming-Ching Shen; Wang J.-D.; Lin C.-Y.; Weng T.-F.; Chiou S.-S.; Peng C.-T.; MING-CHING SHEN
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	2021-05-25T06:35:50Z	A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan	Huang Y.-C.;Shih Y.-H.;Lin C.-Y.;Chiu P.-F.;Kuo S.-F.;Lin J.-S.;Ming-Ching Shen; Huang Y.-C.; Shih Y.-H.; Lin C.-Y.; Chiu P.-F.; Kuo S.-F.; Lin J.-S.; 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
中原大學	2000	Identification of a new CA dinucleotide repeat in the human factor VIII gene	Shu-Rung Lin;Shu-Wha Lin;Ya-Chu Hsu;Ming-Ching Shen
中原大學	1995	Genetic diagnosis of haemophilia A of Chinese origin	Shu-Rung Lin;Shu-Chuan Chang;Chia-Cheng Lee;Ming-Ching Shen;Shu-Wha Lin

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