From Concept to Bedside: What Pediatricians Should Know about Synthesis of Clinical Practice Guidelines?

by Mohamed, Sarar
Published 2014

Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients

by Mohamed, Sarar, Hamad, Muddathir H., Abu-Amero, Khaled K.
Published 2015

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

by Mohamed, Sarar, Osman, Abdaldafae, Al Jurayyan, Nasir A, Al Nemri, Abdulrahman, Salih, Mustafa AM
Published 2014

Glutaric aciduria type 1 as a cause of dystonic cerebral palsy

by Mohamed, Sarar, Hamad, Muddathir H., Hassan, Hamdy H., Salih, Mustafa A.
Published 2015

A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia

by Mohamed, Sarar, Hamad, Muddathir H., Kondkar, Altaf A., Abu-Amero, Khaled K.
Published 2015

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

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

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

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

Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population

by Alharbi, Khalid K, Kashour, Tarek S, Al-Hussaini, Wejdan, Al-Nbaheen, May Salem, Mohamed, Sarar, Hasanato, Rana MW, Tamimi, Waleed, Al-Naami, Mohammed Yahya, Khan, Imran Ali
Published 2013

Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A Mutation

by Houghton, Jayne A.L., Swift, Galvin H., Shaw-Smith, Charles, Flanagan, Sarah E., de Franco, Elisa, Caswell, Richard, Hussain, Khalid, Mohamed, Sarar, Abdulrasoul, Majedah, Hattersley, Andrew T., MacDonald, Raymond J., Ellard, Sian
Published 2016