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1. Aberrant X chromosomal rearrangement through multi‐step template switching during sister chromatid formation in a patient with severe hemophilia A. Issue 9 (5th July 2020)

2. Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing. Issue 179 (July 2019)

3. Clinical conditions and risk factors for inhibitor‐development in patients with haemophilia: A decade‐long prospective cohort study in Japan, J‐HIS2 (Japan Hemophilia Inhibitor Study 2). Issue 5 (11th June 2022)

5. Comparison of the efficacy of ribavirin plus peginterferon alfa‐2b for chronic hepatitis C infection in patients with and without coagulation disorders. Issue 2 (14th November 2012)

6. Essential role of a carboxyl‐terminal α‐helix motif in the secretion of coagulation factor XI. (10th February 2021)

7. F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B. Issue 213 (May 2022)

9. Functional inhibition of MEF2 by C/EBP is a possible mechanism of leukemia development by CEBP‐IGH fusion gene. Issue 3 (27th November 2022)

10. High prophylactic LMWH dose successfully suppressed hemostatic activation in pregnant woman with a new prothrombin c.1787G > A mutation. Issue 2 (February 2015)