Suchergebnisse - "Mizusawa, Yuka"

PubPharm (72)

1

Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram : Sub-Analysis From the SABRUS

enthalten in: Circulation. Arrhythmia and electrophysiology | 2023

von Milman, A. | Sabbag, A. | Conte, G. | +43

2

Author Correction : Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

enthalten in: Nature genetics | 2022

von Barc, J. | Tadros, R. | Glinge, C. | +99

ErratumFor: Nat Genet. 2022 Mar;54(3):232-239. - PMID 35210625

3

Author correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility : amendments

enthalten in: Nature genetics | May 2022

von Barc, J. | Tadros, R. | Glinge, C. | +143

4

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

enthalten in: Nature genetics | 2022

von Barc, J. | Tadros, R. | Glinge, C. | +99

ErratumIn: Nat Genet. 2022 May;54(5):735. - PMID 35474365

5

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility : letters

enthalten in: Nature genetics | March 2022

von Barc, J. | Tadros, R. | Glinge, C. | +143

6

Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands

enthalten in: Circulation. Genomic and precision medicine | 2021

von Milman, A. | Behr, E. | Gray, B. | +41

7

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

enthalten in: Circulation. Genomic and precision medicine | 2020

von Wijeyeratne, Y. | Tanck, M. | Mizusawa, Y. | +42

8

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

enthalten in: Circulation | 2020

von Lahrouchi, N. | Tadros, R. | Crotti, L. | +98

ErratumIn: Circulation. 2020 Jul 28;142(4):e66. - PMID 32718245

9

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

enthalten in: Circulation journal : official journal of the Japanese Circulation Society | 2020

von Kawamura, M. | Ohno, S. | Naiki, N. | +19

ErratumFor: Circ J. 2013;77(7):1705-13. - PMID 23595086

10

Ethnic differences in patients with Brugada syndrome and arrhythmic events : New insights from Survey on Arrhythmic Events in Brugada Syndrome

enthalten in: Heart rhythm | 2019

von Milman, A. | Andorin, A. | Postema, P. | +44

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