Global longitudinal strain detects subtle left ventricular systolic dysfunction in Duchenne muscular dystrophy patients and carriers

por Shehta, Mahmoud, Rayan, Mona Mostafa, Fahmy, Nagia Aly, Onsy, Ahmed, Bastawy, Islam
Publicado 2021

Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG)

por Soliman, Radwa, Rashed, Hebatallah R., Moustafa, Ramez R., Hamdi, Nabila, Swelam, Mahmoud S., Osman, Ahmad, Fahmy, Nagia
Publicado 2023

A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity

por Fahmy, Nagia, Müller, Kathrin, Andersen, Peter Munch, Marklund, Stefan L., Otto, Markus, Ludolph, Albert C., Hamdi, Nabila
Publicado 2022

miRNome profiling in Duchenne muscular dystrophy; identification of asymptomatic and manifesting female carriers

por Mousa, Nahla O., Sayed, Ahmed A., Fahmy, Nagia, Elzayat, Mariam G., Bakry, Usama, Abdellatif, Ahmed, Zahra, Waheed K., Osman, Ahmed
Publicado 2021

Case Report: A Novel AChR Epsilon Variant Causing a Clinically Discordant Salbutamol Responsive Congenital Myasthenic Syndrome in Two Egyptian Siblings

por Gómez-García de la Banda, Marta, Simental-Aldaba, Emmanuel, Fahmy, Nagia, Sternberg, Damien, Blondy, Patricia, Quijano-Roy, Susana, Malfatti, Edoardo
Publicado 2022