Tetsuji Sato

Kitakyushu, Japan

Last Updated: 09/26/2026

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Found 13 publications

Factors Influencing Sport-Induced Bleeding in Patients With Haemophilia Without Inhibitors: A Single Centre Retrospective Study of People Born in the 2000s.

Factors Influencing Sport-Induced Bleeding in Patients With Haemophilia Without Inhibitors: A Single Centre Retrospective Study of People Born in the 2000s.

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

Published: August 10, 2025

Catastrophic antiphospholipid syndrome with Epstein-Barr virus-associated hemophagocytosis: A clinicopathological conference.

Catastrophic antiphospholipid syndrome with Epstein-Barr virus-associated hemophagocytosis: A clinicopathological conference.

Journal: Lupus

Published: August 08, 2022

Hemophilic pseudotumor of the maxillary sinus in an inhibitor-positive patient with hemophilia A receiving emicizumab: a case report.

Hemophilic pseudotumor of the maxillary sinus in an inhibitor-positive patient with hemophilia A receiving emicizumab: a case report.

Journal: International journal of hematology

Published: October 18, 2021

Nintedanib for treatment of progressive interstitial lung disease after peripheral blood stem cell transplantation in a patient with recurrent acute lymphoblastic leukemia.

Nintedanib for treatment of progressive interstitial lung disease after peripheral blood stem cell transplantation in a patient with recurrent acute lymphoblastic leukemia.

Journal: Pediatric blood & cancer

Published: June 18, 2021

Acquired hemophilia A with reappearance of inhibitor 10 years after the completion of immunosuppressive therapy

Acquired hemophilia A with reappearance of inhibitor 10 years after the completion of immunosuppressive therapy

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

Published: April 08, 2021

A Pediatric Case of Acquired Hemophilia A: The Usefulness of the Activated Partial Thromboplastin Time (APTT) Cross-Mixing Test for Early Diagnosis

A Pediatric Case of Acquired Hemophilia A: The Usefulness of the Activated Partial Thromboplastin Time (APTT) Cross-Mixing Test for Early Diagnosis

Journal: Journal of UOEH

Published: December 21, 2018

Correction to: Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.

Correction to: Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.

Journal: International journal of hematology

Published: November 18, 2017

Long-term safety and efficacy of emicizumab in a phase 1/2 study in patients with hemophilia A with or without inhibitors.

Long-term safety and efficacy of emicizumab in a phase 1/2 study in patients with hemophilia A with or without inhibitors.

Journal: Blood advances

Published: March 13, 2017

Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.

Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.

Journal: International journal of hematology

Published: February 16, 2017

The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.

The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.

Journal: Pediatric blood & cancer

Published: June 24, 2016

Factor VIII-Mimetic Function of Humanized Bispecific Antibody in Hemophilia A.

Factor VIII-Mimetic Function of Humanized Bispecific Antibody in Hemophilia A.

Journal: The New England journal of medicine

Published: May 26, 2016

Bernard-Soulier syndrome due to compound heterozygosity for a novel glycoprotein Ibβ mutation.

Bernard-Soulier syndrome due to compound heterozygosity for a novel glycoprotein Ibβ mutation.

Journal: Acta haematologica

Published: December 18, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026