Late presentation of necrotizing enterocolitis associated with rotavirus infection in a term infant with hyperinsulinism on octreotide therapy: A case report

por Alsaedi, Abdulaziz A., Bakkar, Ayman A., Kamal, Naglaa M., Althobiti, Jwaher M.
Publicado 2017

Sotos syndrome: A case report of 1st genetically proven case from Saudi Arabia with a novel mutation in NSD1 gene

por Kamal, Naglaa M., Althobiti, Jwaher M., Alsaedi, Abdulaziz, Bakkar, Ayman, Alkaabi, Tahani
Publicado 2018

Novel Melano-Cortin-2-Receptor Gene Mutation Presenting With Infantile Cholestasis: A Case Report

por Alsaedi, Abdulaziz, Kamal, Naglaa M, Bakkar, Ayman, Althobaiti, Enad, Naeem, Muhammad, Kamal, Mohamed
Publicado 2022

Vici syndrome with pathogenic homozygous EPG5 gene mutation: A case report and literature review

por Abidi, Kamal T., Kamal, Naglaa M., Bakkar, Ayman A., Almarri, Saad, Abdullah, Rehab, Alsufyani, Maram, Alharbi, Arwa
Publicado 2020

Idiopathic hypoparathyroidism with extensive intracranial calcification in children: First report from Saudi Arabia

por Kamal, Naglaa M., Alghamdi, Hamed A., Halabi, Abdulrahman A., Bakkar, Ayman A., Algarni, Ali, Alharbi, Abdullah, Alharthi, Abdulla A., Alharbi, Rawan A., Sherief, Laila M.
Publicado 2017

Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation

por Bakkar, Ayman A, Alsaedi, Abdulaziz, Kamal, Naglaa M, Althobaiti, Enad, Aboulkhair, Lujain A, Almalki, Abdullah M, Alsalmi, Shaima A, Alharthi, Qaydah, Abosabie, Sara A, Abosabie, Salma AS
Publicado 2023

The Impact of COVID-19 Pandemic Lockdown on the Incidence of New-Onset Type 1 Diabetes and Ketoacidosis Among Saudi Children

por Alaqeel, Aqeel, Aljuraibah, Fahad, Alsuhaibani, Mohammed, Huneif, Mohammed, Alsaheel, Abdulhameed, Dubayee, Mohammad Al, Alsaedi, Abdulaziz, Bakkar, Ayman, Alnahari, Ahmed, Taha, Areej, Alharbi, Khulood, Alanazi, Yousef, Almadhi, Samia, Khalifah, Reem Al
Publicado 2021