未登录

N

Nathalie Neyroud

assistance publique hopitaux paris (aphp)

H指数:19

被引数:2,686

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome

基于软件的T波形态分析：识别高风险长QT综合征的心电图特征

IF7.4

2025-09-010

PRE

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients

IF7.4

2024-06-030

OAAI

Methods and applications in cardiac electrophysiology-application to inherited arrhythmias

心脏电生理学中的方法和应用-遗传性心律失常的应用

FRONTIERS IN PHYSIOLOGY

IF3.4

2024-03-060

OAAI

Intracardiac electrophysiology to characterize susceptibility to ventricular arrhythmias in murine models

心内电生理学表征小鼠模型对室性心律失常的敏感性

FRONTIERS IN PHYSIOLOGY

IF3.4

2024-01-230

OAAI

Heterozygous Carriers of KCNQ1 Variants Associated With the Jervell- Lange-Nielsen Syndrome Have a Better Outcome When Compared to Other Type 1 LQTS Patients

IF38.6

2023-11-070

PRE

Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa

FRONTIERS IN BIOSCIENCE-LANDMARK

IF3.1

2022-06-303

OA

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response

与肾上腺素能反应受损相关的螺旋结构域2中的2型兰诺碱受体变体

JOURNAL OF PERSONALIZED MEDICINE

IF3

2021-06-203

OAAI

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

FRONTIERS IN PHYSIOLOGY

IF3.4

2021-05-288

OAAI

A novel gain-of-function mutation in SCN5A responsible for multifocal ectopic Purkinje-related premature contractions

IF3.7

2020-01-2520

OAAI

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

IF5.7

2014-06-0142

OAAI

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits

CARDIOVASCULAR RESEARCH

IF13.3

2012-06-2784

OA

Role of the Cytoplasmic N-Terminal Domain of the Cardiac Sodium Channel Alpha-Subunit

BIOPHYSICAL JOURNAL

IF3.1

2012-01-010

OAAI

Kv4 Potassium Channels Form a Tripartite Complex With the Anchoring Protein SAP97 and CaMKII in Cardiac Myocytes

CIRCULATION RESEARCH

IF16.2

2009-03-2784

OAAI

The Anchoring Protein SAP97 Is Crucial For The Surface Expression Of Shal Kv Potassium Channels And Their Regulation By CaMKII In Cardiac Myocytes

BIOPHYSICAL JOURNAL

IF3.1

2009-02-010

OAAI

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

CARDIOVASCULAR RESEARCH

IF13.3

2007-09-1988

OAAI

Isoform-specific modulation of voltage-gated Na+ channels by calmodulin

钙调蛋白对电压门控Na通道的同工型特异性调节

CIRCULATION RESEARCH

IF16.2

2002-03-08147

OAAI

Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations

IF38.6

2001-02-2782

OAAI

Splicing mutations in KCNQ1 -: A mutation hot spot at codon 344 that produces in frame transcripts

IF38.6

1999-09-0747

OAAI

Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

1999-04-0158

OAAI

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome

CIRCULATION RESEARCH

IF16.2

1999-02-19111

OAAI