Case Report: Distinctive EEG Patterns in SCARB-2 Related Progressive Myoclonus Epilepsy

por Hotait, Mostafa, Dirani, Maya, El Halabi, Tarek, Beydoun, Ahmad
Publicado 2020

A novel possible familial cause of epilepsy of infancy with migrating focal seizures related to SZT2 gene variant

por El Halabi, Tarek, Dirani, Maya, Hotait, Mostafa, Nasreddine, Wassim, Beydoun, Ahmad
Publicado 2021

FARS2 Mutations: More Than Two Phenotypes? A Case Report

por Hotait, Mostafa, Nasreddine, Wassim, El-Khoury, Riyad, Dirani, Maya, Nawfal, Omar, Beydoun, Ahmad
Publicado 2020

Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases

por Refaat, Marwan M., Hassanieh, Sylvana, Ballout, Jad A., Zakka, Patrick, Hotait, Mostafa, Khalil, Athar, Bitar, Fadi, Arabi, Mariam, Arnaout, Samir, Skouri, Hadi, Abchee, Antoine, Abi-Saleh, Bernard, Khoury, Maurice, Massouras, Andreas, Nemer, Georges
Publicado 2019

Swine Atrioventricular Node Ablation Using Stereotactic Radiosurgery: Methods and In Vivo Feasibility Investigation for Catheter‐Free Ablation of Cardiac Arrhythmias

por Refaat, Marwan M., Ballout, Jad A., Zakka, Patrick, Hotait, Mostafa, Al Feghali, Karine A., Gheida, Ibrahim Abu, Saade, Charbel, Hourani, Mukbil, Geara, Fady, Tabbal, Malek, Sfeir, Pierre, Jalbout, Wassim, Al‐Jaroudi, Wael, Jurjus, Abdo, Youssef, Bassem
Publicado 2017