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Internal Medicine (Tokyo, Japan)|July 12, 2019
Elevated Plasma Renin Activity Caused by Accelerated-malignant Hypertension in a Patient with Aldosterone-producing Adenoma Complicated with Renal InsufficiencyTatsuya Maruhashi, Michitaka Amioka, Shinji Kishimoto, et al.Journal of Cardiovascular Pharmacology|September 23, 2016
Dexmedetomidine Depresses Sinoatrial and Atrioventricular Nodal Function Without Any Change in Atrial Fibrillation InducibilityAkinori Sairaku, Yukiko Nakano, Kazuyoshi Suenari, et al.Journal of Cardiovascular Electrophysiology|April 22, 2016
Electrical Remodeling of the Atrioventricular Node Caused by Persistent Atrial Fibrillation in HumansAkinori Sairaku, Yukiko Nakano, Kazuyoshi Suenari, et al.Internal Medicine (Tokyo, Japan)|January 17, 2014
Effect of statin on the 5 years clinical outcomes in dialysis patients treated with sirolimus-eluting stentYuzo Kagawa, Mamoru Toyofuku, Yoshiko Masaoka, et al.Heart Rhythm|January 14, 2020
Predicting atrial fibrillation using a combination of genetic risk score and clinical risk factorsYousaku Okubo, Yukiko Nakano, Hidenori Ochi, et al.Plos One|March 7, 2019
Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrillationMichitaka Amioka, Yukiko Nakano, Hidenori Ochi, et al.International Journal of Cardiology|November 15, 2011
Comparison of heart-type fatty acid binding protein and sensitive troponin for the diagnosis of early acute myocardial infarctionYuzo Kagawa, Mamoru Toyofuku, Yoshiko Masaoka, et al.Plos One|September 5, 2018
Maintenance of low inflammation level by the ZFHX3 SNP rs2106261 minor allele contributes to reduced atrial fibrillation recurrence after pulmonary vein isolationShunsuke Tomomori, Yukiko Nakano, Hidenori Ochi, et al.Internal Medicine (Tokyo, Japan)|September 17, 2014
Causes of very late stent thrombosis investigated using optical coherence tomographyMichitaka Amioka, Nobuo Shiode, Tomoharu Kawase, et al.Journal of Biomedical Science|December 6, 2017
H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promotersHiroya Matsumura, Yukiko Nakano, Hidenori Ochi, et al.Pageof 3