Drug treatment of inborn errors of metabolism: a systematic reviewALFADHEL, Majid; AL-THIHLI, Khalid; MOUBAYED, Hiba et al.Archives of disease in childhood. 2013, Vol 98, Num 6, pp 454-461, issn 0003-9888, 8 p.Article

Eighteen-Year Follow-Up of a Patient With Cobalamin F Disease (cblF): Report and ReviewALFADHEL, Majid; LILLQUIST, Yolanda P; DAVIS, Cynthia et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2571-2577, issn 1552-4825, 7 p.Article

Pre- and Postnatal Findings in a Boy With Duplication of the Bladder and Intestine: Report and ReviewALFADHEL, Majid; PUGASH, Denise; ROBINSON, Ashley James et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2795-2802, issn 1552-4825, 8 p.Article

Infantile Cardioencephalopathy due to a COX15 Gene Defect: Report and ReviewALFADHEL, Majid; LILLQUIST, Yolanda P; WATERS, Paula J et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 4, pp 840-844, issn 1552-4825, 5 p.Article

Transaldolase deficiency: report of 12 new cases and further delineation of the phenotypeEYAID, Wafaa; AL HARBI, Talal; ANAZI, Shamsa et al.Journal of inherited metabolic disease. 2013, Vol 36, Num 6, pp 997-1004, issn 0141-8955, 8 p.Article

Variability of Phenotype in Two Sisters with Pyridoxine Dependent EpilepsyALFADHEL, Majid; SIRRS, Sandra; WATERS, Paula J et al.Canadian journal of neurological sciences. 2012, Vol 39, Num 4, pp 516-519, issn 0317-1671, 4 p.Article