日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1

心电图与电生理检查及强直性肌营养不良1型患者的主要传导延迟

Clementy, Nicolas; Labombarda, Fabien; Grolleau, François; Algalarrondo, Vincent; Bassez, Guillaume; Bécane, Henri-Marc; Béhin, Anthony; Chapon, Françoise; El Hachmi, Mohamed; Fayssoil, Abdallah; Fontaine, Bertrand; Garcia, Rodrigue; Laforêt, Pascal; Lazarus, Arnaud; Masingue, Marion; Magot, Armelle; Pereon, Yann; Probst, Vincent; Motté, Leslie; Saadi, Malika; Duboc, Denis; Stojkovic, Tanya; Porcher, Raphaël; Wahbi, Karim

Cardiac Gene Therapy With Phosphodiesterase 2A Limits Remodeling and Arrhythmias in Mouse Models of Heart Failure.

利用磷酸二酯酶 2A 进行心脏基因治疗可限制小鼠心力衰竭模型中的重塑和心律失常

Kamel Rima, Bourcier Aurélia, Margaria Jean Piero, Jin Valentin, Varin Audrey, Hivonnait Agnès, Mercier-Nomé Françoise, Mika Delphine, Ghigo Alessandra, Charpentier Flavien, Algalarrondo Vincent, Hirsch Emilio, Fischmeister Rodolphe, Vandecasteele Grégoire, Leroy Jérôme

Making Sense of Missense: Benchmarking MutScore for Variant Interpretation in Inherited Cardiac Diseases

解读错义突变:MutScore 在遗传性心脏病变异解读中的基准测试

Porretta, Alessandra Pia; Fressart, Véronique; Surget, Elodie; Morgat, Charles; Bloch, Adrien; Messali, Anne; Algalarrondo, Vincent; Vedrenne, Géraldine; Pruvot, Etienne; Leenhardt, Antoine; Denjoy, Isabelle; Extramiana, Fabrice

Intracutaneous Amyloid Deposition is Associated With Nerve Conduction Studies Deterioration in Presumed Asymptomatic Pathogenic Variant TTR Carriers

皮内淀粉样蛋白沉积与假定无症状致病性TTR变异携带者的神经传导研究结果恶化相关

Schulz, Nina; Beauvais, Diane; Cauquil, Cécile; Labeyrie, Céline; Iliescu, Iulia; Francou, Bruno; Adam, Clovis; Echaniz-Laguna, Andoni; Leonardi, Luca; Algalarrondo, Vincent; Adams, David; Beaudonnet, Guillemette

Left Bundle Branch Area Pacing in Transthyretin Cardiac Amyloidosis: A Narrative Review

左束支区域起搏治疗转甲状腺素蛋白淀粉样变性心脏:叙述性综述

Herrera Bethencourt, Maria; Kristen, Arnt V; Algalarrondo, Vincent; Imnadze, Guram; Müssigbrodt, Andreas

Wide QRS monomorphic tachycardia induced by ajmaline infusion

阿义马林输注诱发的宽QRS单形性心动过速

Laporte, Pierre-Léo; Porretta, Alessandra Pia; Charles, Morgat; Algalarrondo, Vincent; Extramiana, Fabrice

Prediction of late ventricular arrhythmias in patients with left ventricular assist device: insights from the VT-LVAD consortium

预测左心室辅助装置患者晚期室性心律失常:来自 VT-LVAD 联盟的见解

Martins, Raphael; Galand, Vincent; Flecher, Erwan; Groussin, Pierre; Bode, Kerstin; Efimova, Elena; Dashkevich, Alexey; Liang, Jackson; Larson, John; Mondesert, Blandine; Boulet, Jacinthe; Noly, Pierre-Emmanuel; Sacher, Frederic; Pasquié, Jean Luc; Gourraud, Jean-Baptiste; Ninni, Sandro; Jesel, Laurence; Sebestyen, Alexandre; Algalarrondo, Vincent; Deharo, Jean-Claude; Anselme, Frederic; Champ-Rigot, Laure; Guenancia, Charles; Pierre, Bertrand; Eschalier, Romain; Echivard, Mathieu; Baudinaud, Pierre; Lellouche, Nicolas; Gardey, Kevin; Benali, Karim; Gautier, Paul; Delmas, Clément; Cherbi, Miloud

Essential Role of the RIα Subunit of cAMP-Dependent Protein Kinase in Regulating Cardiac Contractility and Heart Failure Development

cAMP依赖性蛋白激酶RIα亚基在调节心肌收缩力和心力衰竭发展中的关键作用

Bedioune, Ibrahim; Gandon-Renard, Marine; Dessillons, Matthieu; Barthou, Aurélien; Varin, Audrey; Mika, Delphine; Bichali, Saïd; Cellier, Joffrey; Lechène, Patrick; Karam, Sarah; Dia, Maya; Gomez, Susana; Pereira de Vasconcelos, Walma; Mercier-Nomé, Françoise; Mateo, Philippe; Dubourg, Audrey; Stratakis, Constantine A; Mercadier, Jean-Jacques; Benitah, Jean-Pierre; Algalarrondo, Vincent; Leroy, Jérôme; Fischmeister, Rodolphe; Gomez, Ana-Maria; Vandecasteele, Grégoire

Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriers

详细的临床、生理和病理表型分析可以影响ATTR基因携带者获得疾病修饰治疗的机会。

Beauvais, Diane; Labeyrie, Céline; Cauquil, Cécile; Francou, Bruno; Eliahou, Ludivine; Not, Adeline; Echaniz-Laguna, Andoni; Adam, Clovis; Slama, Michel S; Benmalek, Anouar; Leonardi, Luca; Rouzet, François; Adams, David; Algalarrondo, Vincent; Beaudonnet, Guillemette

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

KCNQ1 变异体的基因特征分析可改善 1 型长 QT 综合征患者的风险分层

Morgat, Charles; Fressart, Véronique; Porretta, Alessandra Pia; Neyroud, Nathalie; Messali, Anne; Temmar, Yassine; Algalarrondo, Vincent; Surget, Elodie; Bloch, Adrien; Leenhardt, Antoine; Denjoy, Isabelle; Extramiana, Fabrice