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Taisuke Ishikawa

national cerebral & cardiovascular center - japan
H指数:26
被引数:2,286

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Cardiomyopathy Associated with Subclinical Becker Muscular Dystrophy in a Patient Presenting with Anesthesia-induced Rhabdomyolysis

与亚临床贝克肌营养不良相关的心肌病,发生于一名因麻醉诱导性横纹肌溶解而就诊的患者

2025-11-010
PRE
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants

与titan经典剪接位点变异相关的心脏传导障碍和心肌病的表型谱

2025-09-011
PRE
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
2024-05-153
PRE
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
2024-04-202
OAAI
Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
2023-01-016
OAAI
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants
2021-08-018
OA
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
2021-06-0541
PRE
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2021-01-0166
OAAI
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families
2020-12-0150
OAAI
Cardiac Emerinopathy A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction
2020-10-0119
OAAI
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
2020-07-2885
OAAI
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry
2018-10-2525
OAAI
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation
2017-03-0173
OAAI
Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias
2015-10-0151
OAAI