Detalhe da pesquisa
1.
SCN5A mutation identified in a patient with short-coupled variant of torsades de pointes.
Pacing Clin Electrophysiol
; 43(5): 456-461, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32323320
2.
Prevention of postprandial hypotension-related syncope by caffeine in a patient with long-standing diabetes mellitus.
Endocr J
; 67(6): 585-592, 2020 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32115439
3.
Quantitative analysis of PKP2 and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygous PKP2 deletion.
Europace
; 19(4): 644-650, 2017 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28431057
4.
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
5.
High Frequency of Early Repolarization and Brugada-Type Electrocardiograms in Hypercalcemia.
Ann Noninvasive Electrocardiol
; 21(1): 30-40, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26263049
6.
Mechanical alternans in human idiopathic dilated cardiomyopathy is caused with impaired force-frequency relationship and enhanced poststimulation potentiation.
Heart Vessels
; 28(3): 336-44, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22573070
7.
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome.
JACC Clin Electrophysiol
; 8(3): 297-305, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35331424
8.
Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1.
Heart
; 108(11): 840-847, 2022 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35135837
9.
LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy.
Circ Genom Precis Med
; 13(5): 435-443, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32818388
10.
Genetic variants of alcohol-metabolizing enzymes in Brugada syndrome: Insights into syncope after drinking alcohol.
J Arrhythm
; 35(5): 752-759, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31624517
11.
Copy number variations of SCN5A in Brugada syndrome.
Heart Rhythm
; 15(8): 1179-1188, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29574140
12.
Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome.
J Am Heart Assoc
; 7(18): e009387, 2018 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30371189
13.
A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsades de pointes ventricular arrhythmia.
Heart Rhythm
; 14(1): 98-107, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27756708
14.
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.
J Cardiol
; 70(1): 74-79, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27816319
15.
Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
Circ Genom Precis Med
; 14(4): e003223, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34384224
16.
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.
Intern Med
; 55(3): 259-62, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26831020
17.
Frequency characteristics and associations with the defibrillation threshold of ventricular fibrillation in patients with implantable cardioverter defibrillators.
Intern Med
; 54(10): 1175-82, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25986253
18.
Benign premature ventricular complexes from the right ventricular outflow tract triggered polymorphic ventricular tachycardia in a latent type 2 LQTS patient.
Intern Med
; 51(23): 3261-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23207121
19.
An appropriate defibrillation threshold obtained by the combined connection between two shock leads and ICD generator.
Intern Med
; 50(22): 2815-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22082895
20.
Augmentation of the J wave by rapid pacing in a patient with vasospastic angina.
Int J Cardiol
; 172(1): e111-3, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24438938