Han-ni Hsieh
Chang-hua, TNQ, Taiwan
Last Updated: 09/26/2026
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Found 12 publications
Non-Inversion Variants in Sporadic Hemophilia A Rarely Recur.
Journal: International journal of molecular sciences
Published: February 10, 2026
Congenital Factor XIII Deficiency in Taiwan: A Novel F13A1 p.Lys113* Variant Identified in a Patient With an Inhibitor and Our Experience to Induce Immune Tolerance.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: September 13, 2024
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: November 22, 2023
Deep vein thrombosis after open hepatectomy or other major upper abdominal surgery in Taiwan: A prospective and cross-sectional study relevant to the issue of pharmacological thromboprophylaxis.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: October 21, 2022
Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: August 10, 2022
Deep vein thrombosis after major orthopedic surgery in Taiwan: A prospective cross-sectional study and literature review.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: November 16, 2021
Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation.
Journal: International journal of hematology
Published: November 16, 2021
First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene.
Journal: International journal of hematology
Published: October 29, 2020
Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: March 05, 2020
Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent.
Journal: Pediatric hematology and oncology
Published: February 01, 2019
De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD.
Journal: Thrombosis journal
Published: October 22, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026