Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels

por Amarouch, Mohamed-Yassine, Abriel, Hugues
Publicado 2015

Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies

por Amarouch, Mohamed-Yassine, El Hilaly, Jaouad
Publicado 2020

AFM and FluidFM Technologies: Recent Applications in Molecular and Cellular Biology

por Amarouch, Mohamed Yassine, El Hilaly, Jaouad, Mazouzi, Driss
Publicado 2018

Biophysical Characterization of Epigallocatechin-3-Gallate Effect on the Cardiac Sodium Channel Na(v)1.5

por Amarouch, Mohamed-Yassine, Kurt, Han, Delemotte, Lucie, Abriel, Hugues
Publicado 2020

Editorial: Inherited Arrhythmias of the Cardiac Sodium Channel Na(v)1.5

por Amarouch, Mohamed-Yassine, Zaklyazminskaya, Elena V., Rougier, Jean-Sébastien
Publicado 2021

Functional interaction between S1 and S4 segments in voltage-gated sodium channels revealed by human channelopathies

por Amarouch, Mohamed-Yassine, Kasimova, Marina A, Tarek, Mounir, Abriel, Hugues
Publicado 2014

Exposition au mercure et état de santé des médecins dentistes de deux régions du centre du Maroc: enquête transversale descriptive

por Attiya, Nourdine, Fattahi, Rkia, El-Haidani, Ahmed, Lahrach, Nadia, Amarouch, Mohamed-Yassine, Filali-Zegzouti, Younes
Publicado 2020

Modeling Subjective Symptoms Related to Micro-Hydrargyrism in a Population of Moroccan Dentists

por Attiya, Nourdine, Filali, Ayoub, Fattahi, Rkia, Moujane, Soumia, Mazouz, Hamid, Amarouch, Mohamed-Yassine, Filali-Zegzouti, Younes
Publicado 2021

In Silico Evaluation of the Potential Antiarrhythmic Effect of Epigallocatechin-3-Gallate on Cardiac Channelopathies

por Boukhabza, Maroua, El Hilaly, Jaouad, Attiya, Nourdine, El-Haidani, Ahmed, Filali-Zegzouti, Younes, Mazouzi, Driss, Amarouch, Mohamed-Yassine
Publicado 2016

Psychometric properties of Clinical Learning Environment Inventory and its association with Moroccan nursing students’ satisfaction: A PLS-SEM approach

por Saka, Khadija, Amarouch, Mohamed-Yassine, Ragala, Mohamed El Amine, Btissame, Zarrouq, Tahraoui, Adel, El Achhab, Youness, El-Hilaly, Jaouad
Publicado 2023

Complex genetic background in a large family with Brugada syndrome

por Saber, Siamak, Amarouch, Mohamed‐Yassine, Fazelifar, Amir‐Farjam, Haghjoo, Majid, Emkanjoo, Zahra, Alizadeh, Abolfath, Houshmand, Massoud, Gavrilenko, Alexander V., Abriel, Hugues, Zaklyazminskaya, Elena V.
Publicado 2015

Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block

por Syam, Ninda, Chatel, Stéphanie, Ozhathil, Lijo Cherian, Sottas, Valentin, Rougier, Jean‐Sébastien, Baruteau, Alban, Baron, Estelle, Amarouch, Mohamed‐Yassine, Daumy, Xavier, Probst, Vincent, Schott, Jean‐Jacques, Abriel, Hugues
Publicado 2016

A Long QT Mutation Substitutes Cholesterol for Phosphatidylinositol-4,5-Bisphosphate in KCNQ1 Channel Regulation

por Coyan, Fabien C., Abderemane-Ali, Fayal, Amarouch, Mohamed Yassine, Piron, Julien, Mordel, Jérôme, Nicolas, Céline S., Steenman, Marja, Mérot, Jean, Marionneau, Céline, Thomas, Annick, Brasseur, Robert, Baró, Isabelle, Loussouarn, Gildas
Publicado 2014