Co-occurrence of Glycogen Storage Disease Type 2 and Congenital Myasthenic Syndrome Type 5 in a Pediatric Patient: A Case Report

por Al-Sharif, Fawzia, Alamer, Mohammed F, Taher, Hussein O, Gazzaz, Raneem Y, AlRuwaithi, Asma O, Miliany, Tuleen T, Alrufaihi, Mohammed A, Al Amer, Abdullah F
Publicado 2022

Heterozygous Mutation of Sodium Voltage-Gated Channel Alpha Subunit 2 and Pumilio Homolog 1 Genes in a Pediatric Patient: A Case Report

por Al-Sharif, Fawzia, Attiah, Feryal O, AlKhateeb, Nada A, Taher, Hussein o, Alamer, Mohammed F, Gazzaz, Raneem y, Ba Sahel, Muayad o, Alsharif, Rena M
Publicado 2022

Retroperitoneal Lipoma: An Unusual Etiology of Urge Incontinence

por Alamer, Mohammed F, Alhuthaly, Saud K, Alfahhad, Mohanned F, Taher, Hussein O, Gazzaz, Raneem Y, Miliany, Tuleen T, Alsulaiman, Abdullah S, Almohaimeed, Latifah Y, Almadwi, Rabab S, Qadah, Zeyad A, Alfaqih, Omar M, Alshammari, Raed K, Alsharif, Eid M, Al-Dablan, Mohammed S, Al-Hawaj, Faisal
Publicado 2021

Expression of Concern: Retroperitoneal Lipoma: An Unusual Etiology of Urge Incontinence

por Alamer, Mohammed F, Alhuthaly, Saud K, Alfahhad, Mohanned F, Taher, Hussein O, Gazzaz, Raneem Y, Miliany, Tuleen T, Alsulaiman, Abdullah S, Almohaimeed, Latifah Y, Almadwi, Rabab S, Qadah, Zeyad A, Alfaqih, Omar M, Alshammari, Raed K, Alsharif, Eid M, Al-Dablan, Mohammed S, Al-Hawaj, Faisal
Publicado 2022