Toshiyuki Miyata

Osaka, Japan

Last Updated: 09/26/2026

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Found 103 publications

Complement-coagulation crosstalk in immunothrombosis

Complement-coagulation crosstalk in immunothrombosis

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

Published: August 30, 2026

FXII Frameshift Variant Does Not Cause Hereditary Angioedema with Normal C1 Inhibitor.

FXII Frameshift Variant Does Not Cause Hereditary Angioedema with Normal C1 Inhibitor.

Journal: Journal of clinical immunology

Published: October 18, 2025

The C3 p.Ile1157Thr mutation associated with atypical hemolytic uremic syndrome, particularly in Japan, does not lead to disease development in several mouse models.

The C3 p.Ile1157Thr mutation associated with atypical hemolytic uremic syndrome, particularly in Japan, does not lead to disease development in several mouse models.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 23, 2025

Evaluation of Deficiency and Excessive Condition of Thrombin Burst Using Laboratory Tests.

Evaluation of Deficiency and Excessive Condition of Thrombin Burst Using Laboratory Tests.

Journal: Thrombosis and haemostasis

Published: September 18, 2025

Thrombus Age in Ischemic Stroke With Atrial Fibrillation: Impact on Mechanical Thrombectomy.

Thrombus Age in Ischemic Stroke With Atrial Fibrillation: Impact on Mechanical Thrombectomy.

Journal: Stroke (Hoboken, N.J.)

Published: June 24, 2024

Familial onset of venous thromboembolism due to inherited antithrombin deficiency with a novel gene variant (p.Arg14Gly).

Familial onset of venous thromboembolism due to inherited antithrombin deficiency with a novel gene variant (p.Arg14Gly).

Journal: Journal of cardiology cases

Published: October 03, 2023

Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) in Japan 2023.

Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) in Japan 2023.

Journal: International journal of hematology

Published: June 06, 2023

Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency.

Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency.

Journal: Allergology international : official journal of the Japanese Society of Allergology

Published: March 23, 2023

Fibrin and fibrinogen degradation products/D-dimer ratio can be a useful marker for differentiating an acute attack of hereditary angioedema from thrombotic conditions.

Fibrin and fibrinogen degradation products/D-dimer ratio can be a useful marker for differentiating an acute attack of hereditary angioedema from thrombotic conditions.

Journal: Allergology international : official journal of the Japanese Society of Allergology

Published: March 12, 2023

Three Cases of Unprovoked Venous Thromboembolism with Prothrombin p.Arg596Gln Variant and a Literature Review of Antithrombin Resistance.

Three Cases of Unprovoked Venous Thromboembolism with Prothrombin p.Arg596Gln Variant and a Literature Review of Antithrombin Resistance.

Journal: Internal medicine (Tokyo, Japan)

Published: August 09, 2022

P2Y12 Reaction Units and Clinical Outcomes in Acute Large Artery Atherosclerotic Stroke: A Multicenter Prospective Study.

P2Y12 Reaction Units and Clinical Outcomes in Acute Large Artery Atherosclerotic Stroke: A Multicenter Prospective Study.

Journal: Journal of atherosclerosis and thrombosis

Published: March 07, 2022

Influence of Renal Impairment and Genetic Subtypes on Warfarin Control in Japanese Patients.

Influence of Renal Impairment and Genetic Subtypes on Warfarin Control in Japanese Patients.

Journal: Genes

Published: August 29, 2021

Showing 1-12 of 103

Last Updated: 09/26/2026