臺灣基因治療學會_理事

理事周聖傑

專業證照
  • 西醫師
  • 內科專科醫師
  • 血液科專科醫師
學歷
  • 慈濟大學醫學系畢
經歷
  1. 國立台灣大學醫學院附設醫院主治醫師
  2. 國立台灣大學醫學院講師
專長領域
  1. 血液凝固學
  2. 血友病基因治療
專業著作
  • Chou SC, Yen CT, Yang YL, Chen SH, Wang JD, Fan MN, Chen LF, Yu IS, Tsai DY, Lin KI, Tao MH, Wu JC, Lin SW. Recapitulating the immune system of hemophilia A patients with inhibitors using immunodeficient mice.Thromb Res. 2024; 235: 155-63. 10.1016/j.thromres.2024.01.019.
  • Mahlangu J, Kaczmarek R, von Drygalski A, Shapiro S, Chou SC, Ozelo MC, et al.Two-Year Outcomes of Valoctocogene Roxaparvovec Therapy for Hemophilia A. New England Journal of Medicine. 2023; 388: 694-705. 10.1056/NEJMoa2211075.
  • Shen MC, Chou SC, Chiou SS, Lin PC, et al, Taiwan Society of T, Hemostasis study g. Efficacy, safety and cost of emicizumab prophylaxis in haemophilia A patients with inhibitors: A nationwide observational study in Taiwan. Haemophilia. 2023. 10.1111/hae.14880.
  • Chou SC, Hsu YC, Lin SW. Gene therapy for hemophilia, a clinical viewpoint. J Formos Med Assoc. 2023; 122: 1101-10. 10.1016/j.jfma.2023.05.008.
  • Chou SC, Pai CH, Lin SW, Tien HF. Incidence and risk factors for venous thromboembolism in a cohort of Taiwanese patients with lung, gastric, pancreatic cancers or lymphoma. J Formos Med Assoc. 2022; 121: 360-6.10.1016/j.jfma.2021.04.025.
  • Chou SC, Chang YC, Liao CK, Chen TC, et al New presentations and exacerbations of immune thrombocytopenia after coronavirus disease 2019 vaccinations: the Taiwan experience. Platelets. 2022; 33: 531-5. 10.1080/09537104.2022.2042237.
  • Chou SC, Lin CY, Lin HY, Pai CH, et al. Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation. Int J Hematol. 2022; 116: 528-33. 10.1007/s12185-022-03390-0.
  • Chou SC, Lin CY, Yen CT, Hsieh HN, et al. Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan. J Formos Med Assoc. 2021; 120: 411-4. 10.1016/j.jfma.2020.05.032.
  • Chou SC, Lin DT, Lin CY, Huang YC, et al. First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene. Int J Hematol. 2021; 113: 760-4. 10.1007/s12185-020-03068-5.
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