Hiroshi Inaba

Tokyo, Japan

Last Updated: 09/26/2026

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Found 16 publications

Assay Discrepancy in Factor IX Activity in Haemophilia B and the Unique Assay Characteristics of FIX: p.Ala74Pro.

Assay Discrepancy in Factor IX Activity in Haemophilia B and the Unique Assay Characteristics of FIX: p.Ala74Pro.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: November 08, 2024

Comparison of genotypes and phenotypes for von Willebrand factor gene variants using Japanese genome database.

Comparison of genotypes and phenotypes for von Willebrand factor gene variants using Japanese genome database.

Journal: Blood vessels, thrombosis & hemostasis

Published: October 30, 2024

Genome editing of patient-derived iPSCs identifies a deep intronic variant causing aberrant splicing in hemophilia A.

Genome editing of patient-derived iPSCs identifies a deep intronic variant causing aberrant splicing in hemophilia A.

Journal: Blood advances

Published: May 30, 2023

Comprehensive comparison of global coagulation assays to differentiate lupus anticoagulant from acquired hemophilia A in patients with prolonged APTT.

Comprehensive comparison of global coagulation assays to differentiate lupus anticoagulant from acquired hemophilia A in patients with prolonged APTT.

Journal: International journal of hematology

Published: May 10, 2023

In vitro validation of chromogenic substrate assay for evaluation of surrogate FVIII-activity of emicizumab.

In vitro validation of chromogenic substrate assay for evaluation of surrogate FVIII-activity of emicizumab.

Journal: Thrombosis research

Published: October 17, 2022

Prolonged α-thrombin-related activation and delayed active protein C-associated degradation confer mild phenotype in a patient with severe hemophilia A with F8 p.H118R.

Prolonged α-thrombin-related activation and delayed active protein C-associated degradation confer mild phenotype in a patient with severe hemophilia A with F8 p.H118R.

Journal: International journal of hematology

Published: December 24, 2021

Coagulation assay discrepancies in Japanese patients with non-severe hemophilia A.

Coagulation assay discrepancies in Japanese patients with non-severe hemophilia A.

Journal: International journal of hematology

Published: July 21, 2021

PAM-flexible Cas9-mediated base editing of a hemophilia B mutation in induced pluripotent stem cells.

PAM-flexible Cas9-mediated base editing of a hemophilia B mutation in induced pluripotent stem cells.

Journal: Communications medicine

Published: February 23, 2021

Properties and Classification of Diamond-Like Carbon Films.

Properties and Classification of Diamond-Like Carbon Films.

Journal: Materials (Basel, Switzerland)

Published: November 21, 2020

Genetic analysis of carrier status in female members of Japanese hemophilia families.

Genetic analysis of carrier status in female members of Japanese hemophilia families.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 07, 2020

Exhaustive analysis of genetic mutations associated with protein S deficiency utilizing next-generation sequencing analysis

Exhaustive analysis of genetic mutations associated with protein S deficiency utilizing next-generation sequencing analysis

Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology

Published: May 10, 2019

Cross-reacting Material-positive Hemophilia A Diagnosed in a Patient with a Spontaneous Thigh Hemorrhage.

Cross-reacting Material-positive Hemophilia A Diagnosed in a Patient with a Spontaneous Thigh Hemorrhage.

Journal: Internal medicine (Tokyo, Japan)

Published: July 05, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026