Congenital toxoplasmosis presenting as central diabetes insipidus in an infant: a case report

por Mohamed, Sarar, Osman, Abdaldafae, Al Jurayyan, Nasir A, Al Nemri, Abdulrahman, Salih, Mustafa AM
Publicado 2014

COVID-19 infection prevalence in pediatric population: Etiology, clinical presentation, and outcome

por Alsohime, Fahad, Temsah, Mohamad-Hani, Al-Nemri, Abdulrahman M., Somily, Ali M., Al-Subaie, Sarah
Publicado 2020

A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia: Molecular genetics report from Saudi Arabia

por Mohamed, Sarar, El-Kholy, Suzan, Al-Juryyan, Nasir, Al-Nemri, Abdulrahman M., Abu-Amero, Khaled K.
Publicado 2015

Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy

por Mohamed, Sarar, Kambal, Mohammed A, Al Jurayyan, Nasir A, Al-Nemri, Abdulrahman, Babiker, Amir, Hasanato, Rana, Al-Jarallah, Abdullah S
Publicado 2013

Practical guidelines for screening and treatment of retinopathy of prematurity in Saudi Arabia

por Al Amro, Saleh A., Al Aql, Fahad, Al Hajar, Saad, Al Dhibi, Hassan, Al Nemri, Abdulrahman, Mousa, Ahmed, Ahmad, Jawwad
Publicado 2018

Perinatal and neonatal morbidity among infants of diabetic mothers at a university hospital in Central Saudi Arabia

por Al-Nemri, Abdulrahman M., Alsohime, Fahd, Shaik, Asfaq H., El-Hissi, Ghasan A., Al-Agha, Mohammed I., Al-Abdulkarim, Nada F., Mohamed, Sarar
Publicado 2018

A novel pathogenic mutation of the CYP27B1 gene in a patient with vitamin D-dependent rickets type 1: a case report

por Babiker, Amir MI, Al Gadi, Iman, Al-Jurayyan, Nasir AM, Al Nemri, Abdulrahman MH, Al haboob, Ali Abdu N, Al Boukai, Ahmed Amer, Al Zahrani, Ali, Habib, Hanan Ahmed
Publicado 2014