Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients
Lin, Hsuan‐Yu, Lin, Ching‐Yeh, Kuo, Su‐Feng, Lin, Jen‐Shiou, Lin, Po‐Te, Huang, Ying‐Chih, Hsieh, Han‐Ni, Shen, Ming‐Ching
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2024)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2024)
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Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population
Shen, Ming‐Ching, Wang, Jiaan‐Der, Tsai, Woei, Lin, Ching‐Yeh, Lin, Jen‐Shiou, Kuo, Su‐Feng, Lin, Po‐Te, Huang, Ying‐Chih, Hung, Mei‐Hua
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2021)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2021)
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Journal Article
Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations
Lin, Hsuan-Yu, Lin, Ching-Yeh, Hung, Mei-Hua, Kuo, Su-Feng, Lin, Jen-Shiou, Shen, Ming-Ching
Published in International journal of hematology (01.08.2020)
Published in International journal of hematology (01.08.2020)
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A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan
Huang, Ying-Chih, Shih, Yu-Hung, Lin, Ching-Yeh, Chiu, Ping-Fang, Kuo, Su-Feng, Lin, Jen-Shiou, Shen, Ming-Ching
Published in International journal of hematology (01.12.2020)
Published in International journal of hematology (01.12.2020)
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Journal Article
Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation
Chou, Sheng-Chieh, Lin, Ching-Yeh, Lin, Hsuan-Yu, Pai, Chen-Hsueh, Yu, Cheng-Ye, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Hung, Mei-Hua, Hsieh, Han-Ni, Liu, Hsiang-Chun, Shen, Ming-Ching
Published in International journal of hematology (01.10.2022)
Published in International journal of hematology (01.10.2022)
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A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review
Shih, Yu-Hung, Huang, Ying-Chih, Lin, Ching-Yeh, Lin, Hsuan-Yu, Kuo, Su-Feng, Lin, Jen-Shiou, Shen, Ming-Ching
Published in Medicine (Baltimore) (27.01.2023)
Published in Medicine (Baltimore) (27.01.2023)
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Journal Article
Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians
Lin, Hsuan-Yu, Lin, Ching-Yeh, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Huang, Ying-Chih, Hsieh, Han-Ni, Shen, Ming-Ching
Published in Blood coagulation & fibrinolysis (01.01.2023)
Published in Blood coagulation & fibrinolysis (01.01.2023)
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