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Pediatric Hematology and Oncology|February 1, 2019
Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parentMing-Ching Shen, Ming Chen, Shung-Ping Chang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|April 4, 2015
A study of 65 patients with acquired hemophilia A in TaiwanShang-Yi Huang, Woei Tsay, Shyuann-Yuh Lin, et al.
Journal of Cellular and Molecular Medicine|October 13, 2022
Origin and timing of de novo variants implicated in type 2 von Willebrand diseaseMing Chen, Ming-Ching Shen, Shun-Ping Chang, et al.
International Journal of Hematology|January 2, 2021
First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 geneSheng-Chieh Chou, Dong-Tasmn Lin, Ching-Yeh Lin, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|November 4, 2025
Heterogeneous Hemostatic Disorder Associated with IgA Monoclonal Gammopathy: A Case SeriesCheng-Wei Huang, Guan-Min Lai, Ching-Yeh Lin, et al.
International Journal of Hematology|April 26, 2020
Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutationsHsuan-Yu Lin, Ching-Yeh Lin, Mei-Hua Hung, et al.
International Journal of Hematology|July 10, 2009
Superwarfarin intoxication: hematuria is a major clinical manifestationYi-Feng Wu, Cheng-Shyong Chang, Chih-Yuan Chung, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|October 3, 2007
Hyperhomocysteinemia, deep vein thrombosis and vitamin B12 deficiency in a metformin-treated diabetic patientHsuan-Yu Lin, Chih-Yuan Chung, Cheng-Shyong Chang, et al.
Thrombosis Journal|October 22, 2016
<i>De novo</i> mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWDMing-Ching Shen, Ming Chen, Gwo-Chin Ma, et al.
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