Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
2021 | Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan | SHENG-CHIEH CHOU ; Lin, Ching-Yeh; Yen, Ching-Tzu; Hsieh, Han-Ni; Huang, Ying-Chih; KO-JEN LI ; SHU-WHA LIN ; MING-CHING SHEN | Journal of the Formosan Medical Association = Taiwan yi zhi | 0 | 0 | |
2021 | Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population | MING-CHING SHEN ; Wang, Jiaan-Der; Tsai, Woei; Lin, Ching-Yeh; Lin, Jen-Shiou; Kuo, Su-Feng; Lin, Po-Te; Huang, Ying-Chih; Hung, Mei-Hua | Haemophilia : the official journal of the World Federation of Hemophilia | 1 | 1 | |
2023 | 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; MING-CHING SHEN | Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 0 | 0 | |
2022 | Deep vein thrombosis after major orthopedic surgery in Taiwan: A prospective cross-sectional study and literature review | Lin, Hsuan-Yu; Lin, Ching-Yeh; Huang, Ying-Chih; Hsieh, Han-Ni; YA-WUN YANG; Chang, Ing-Lin; MING-CHING SHEN | Journal of the Formosan Medical Association = Taiwan yi zhi | 6 | 0 | |
2021 | A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families | Lin, Hsuan-Yu; Lin, Jen-Shiou; WOEI TSAY ; Lin, Po-Te; Huang, Ying-Chih; MING-CHING SHEN | Haemophilia : the official journal of the World Federation of Hemophilia | 1 | 1 | |
2021 | First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene | SHENG-CHIEH CHOU ; Lin, Dong-Tasmn; Lin, Ching-Yeh; Huang, Ying-Chih; Hsieh, Han-Ni; MING-CHING SHEN | International journal of hematology | 0 | 0 | |
2023 | 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; MING-CHING SHEN | Medicine | 0 | 0 | |
2022 | Origin and timing of de novo variants implicated in type 2 von Willebrand disease | MING CHEN; MING-CHING SHEN ; Chang, Shun-Ping; Ma, Gwo-Chin; Huang, Ying-Chih; Lin, Ching-Yeh | Journal of cellular and molecular medicine | 1 | 0 | |
2014 | 白血病病人接受異體造血幹細胞移植後之身體心像
與生活品質之相關因素探討 | 黃盈芷; Huang, Ying-Chih | | | | |