Detalhe da pesquisa
1.
Efficacy and Tolerability of Ivabradine for Cardiomyopathy in Patients with Duchenne Muscular Dystrophy.
Int Heart J
; 65(2): 211-217, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38556332
2.
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Genet Med
; 23(1): 47-58, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893267
3.
Differences in Pharmaceutical Intervention Triggers for the Optimization of Medication by Patient Age: A University Hospital Study.
Biol Pharm Bull
; 44(8): 1060-1066, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34334491
4.
Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutation.
J Electrocardiol
; 69: 111-118, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34656916
5.
Extracorporeal membrane oxygenation for the anesthetic management of a patient with severe airway stenosis caused by thyroid carcinoma invasion.
Surg Today
; 51(12): 2000-2005, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34232373
6.
High incidence of major bleeding with off-label use of edoxaban.
J Clin Biochem Nutr
; 69(3): 311-316, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34857995
7.
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation.
Br J Clin Pharmacol
; 84(6): 1301-1312, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29457840
8.
Impact of ABCB1, ABCG2, and CYP3A5 polymorphisms on plasma trough concentrations of apixaban in Japanese patients with atrial fibrillation.
Pharmacogenet Genomics
; 27(9): 329-336, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28678049
9.
JCS/JHRS 2020 Guideline on Pharmacotherapy of Cardiac Arrhythmias.
Circ J
; 86(11): 1790-1924, 2022 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35283400
10.
The genetics underlying acquired long QT syndrome: impact for genetic screening.
Eur Heart J
; 37(18): 1456-64, 2016 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26715165
11.
Pediatric Cohort With Long QT Syndromeã- KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms.
Circ J
; 80(3): 696-702, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26823142
12.
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes.
Circ J
; 80(12): 2435-2442, 2016 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27784853
13.
Directional bleb formation in spherical cells under temperature gradient.
Biophys J
; 109(2): 355-64, 2015 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26200871
14.
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
Circ J
; 84(11): 2123, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33100285
15.
A Common Mutation of Long QT Syndrome Type 1 in Japan.
Circ J
; 79(9): 2026-30, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26118460
16.
Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan.
Circ J
; 84(11): 2124-2126, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33100286
17.
Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench.
J Cardiovasc Electrophysiol
; 25(1): 66-73, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24112685
18.
Gain-of-function KCNH2 mutations in patients with Brugada syndrome.
J Cardiovasc Electrophysiol
; 25(5): 522-530, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24400717
19.
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.
Europace
; 16(12): 1828-37, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24728418
20.
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.
Europace
; 16(11): 1646-54, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24394973