| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2020 | Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan | Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; SHU-WHA LIN ; Shen M.-C. | Journal of the Formosan Medical Association | 0 | 0 | |
| 2021 | Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan | SHENG-CHIEH CHOU ; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; Lin S.-W.; Shen M.-C. | Journal of the Formosan Medical Association | 0 | ||
| 2021 | Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan | Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; Lin S.-W.; MING-CHING SHEN | Journal of the Formosan Medical Association | 0 | ||
| 2021 | First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene | Chou S.-C.; Lin D.-T.; Lin C.-Y.; Huang Y.-C.; Hsieh H.-N.; MING-CHING SHEN | International Journal of Hematology | 0 | ||
| 2016 | De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD | MING-CHING SHEN ; Chen M.; Ma G.-C.; Chang S.-P.; Lin C.-Y.; Lin B.-D.; Hsieh H.-N. | Thrombosis Journal | 0 | ||
| 2018 | Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent | MING-CHING SHEN ; Chen M.; Chang S.-P.; Lin P.-T.; Hsieh H.-N.; Lin K.-H. | Pediatric Hematology and Oncology | 0 |
