Detalhe da pesquisa
1.
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
Eur Heart J
; 44(35): 3357-3370, 2023 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37528649
2.
Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome.
Europace
; 25(4): 1491-1499, 2023 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36861347
3.
Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome.
Circ J
; 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38044147
4.
Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention.
Circ J
; 87(6): 755-763, 2023 05 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36792180
5.
Calmodulinopathy in Japanese Childrenã- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.
Circ J
; 87(12): 1828-1835, 2023 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37380439
6.
School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome.
Europace
; 24(9): 1496-1503, 2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35060598
7.
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome.
Europace
; 24(3): 497-510, 2022 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34661651
8.
Impact of statin therapy on late target lesion revascularization after everolimus-eluting stent implantation according to pre-interventional vessel remodeling and vessel size of treated lesion.
Heart Vessels
; 37(11): 1817-1828, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35726035
9.
An NGS-based genotyping in LQTS; minor genes are no longer minor.
J Hum Genet
; 65(12): 1083-1091, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681117
10.
High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8.
Circ J
; 84(4): 559-568, 2020 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32161207
11.
Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population.
Circ J
; 84(9): 1575-1581, 2020 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32713878
12.
Novel SCN10A variants associated with Brugada syndrome.
Europace
; 18(6): 905-11, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25842276
13.
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
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.
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
17.
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
18.
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.
Heart Rhythm
; 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38367891
19.
Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Circ J
; 77(6): 1534-42, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23514727
20.
L-type calcium channel mutations in Japanese patients with inherited arrhythmias.
Circ J
; 77(7): 1799-806, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23575362