27 February 2018
Hamad Medical Corporation’s (HMC) Head of Clinical and Metabolic Genetics says early detection is the key to successfully managing rare conditions like Homocystinuria,  a serious genetic disease...
30 April 2017
To highlight the importance of early diagnosis, treatment and prevention of the long-term complications of homocystinuria (HCU) – a rare but potentially serious inherited condition - Hamad Medical...
10 December 2014
Ways of promoting innovative collaborations and simulations for focused research leading to new treatments of hyperammonemia (a metabolic disturbance due to excess ammonia in the blood) and related...
Subscribe to Tawfeg Ben-Omran