Mohammed A Kambal

Mitchell-Riley Syndrome Due to a Novel Mutation in RFX6

Mohammed A Kambal, Doha Ayed Al-Harbi, Areej Al-Sunaid, 2019, Front. Pediatr..

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

Mohammed A Kambal, A. Babiker, R. Hasanato, 2013, BMC Research Notes.

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

Mohammed A Kambal, A. Babiker, R. Hasanato, 2013, BMC Research Notes.

Managing traumatic brain injury in children: When do we need a computed tomography of the head?

Mohammed A Kambal, A. Babiker, A. A. Al Boukai, 2014, Sudanese journal of paediatrics.