Hiroya Matsumura
Onomichi, Japan
Last Updated: 09/26/2026
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Found 25 publications
Impact of SGLT2 inhibitors on old age patients with heart failure and chronic kidney disease.
Journal: International journal of cardiology
Published: March 25, 2022
Intra-procedural anticoagulation and post-procedural hemoglobin fall in atrial fibrillation ablation with minimally interrupted direct oral anticoagulants: comparisons across 4 drugs.
Journal: Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
Published: June 22, 2020
Remaining activity of temporary interrupted direct oral anticoagulants and its impact on intra-ablation heparinization in patients with atrial fibrillation: Comparisons across four drugs and two dose regimens.
Journal: Journal of cardiovascular electrophysiology
Published: January 27, 2020
Residual anticoagulation activity in atrial fibrillation patients with temporary interrupted direct oral anticoagulants: Comparisons across 4 drugs.
Journal: Thrombosis research
Published: July 03, 2019
A mimic of tachycardia-bradycardia syndrome in a patient with long-standing persistent atrial fibrillation.
Journal: Clinical case reports
Published: September 21, 2018
Chromosome 4q25 Variant rs6817105 Bring Sinus Node Dysfunction and Left Atrial Enlargement.
Journal: Scientific reports
Published: February 19, 2018
In Paroxysmal Atrial Fibrillation Patients, the Neutrophil-to-lymphocyte Ratio Is Related to Thrombogenesis and More Closely Associated with Left Atrial Appendage Contraction than with the Left Atrial Body Function.
Journal: Internal medicine (Tokyo, Japan)
Published: November 21, 2017
HCN4 Gene Polymorphisms Are Associated With Occurrence of Tachycardia-Induced Cardiomyopathy in Patients With Atrial Fibrillation.
Journal: Circulation. Genomic and precision medicine
Published: October 08, 2017
Diagnostic performance of the N-terminal pro-brain natriuretic peptide to detect an increased left atrial pressure in patients with persistent atrial fibrillation.
Journal: Clinical chemistry and laboratory medicine
Published: October 07, 2017
H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
Journal: Journal of biomedical science
Published: July 17, 2017
Last Updated: 09/26/2026