Phenotypic variability to medication management: an update on fragile X syndrome

por Elhawary, Nasser A., AlJahdali, Imad A., Abumansour, Iman S., Azher, Zohor A., Falemban, Alaa H., Madani, Wefaq M., Alosaimi, Wafaa, Alghamdi, Ghydda, Sindi, Ikhlas A.
Publicado 2023

Genetic etiology and clinical challenges of phenylketonuria

por Elhawary, Nasser A., AlJahdali, Imad A., Abumansour, Iman S., Elhawary, Ezzeldin N., Gaboon, Nagwa, Dandini, Mohammed, Madkhali, Abdulelah, Alosaimi, Wafaa, Alzahrani, Abdulmajeed, Aljohani, Fawzia, Melibary, Ehab M., Kensara, Osama A.
Publicado 2022

Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community

por Mufti, Ahmad H, AlJahdali, Imad A, Elhawary, Nasser A, Ekram, Samar N, Abumansour, Iman, Sindi, Ikhlas A, Naffadi, Hind, Elhawary, Ezzeldin N, Alyamani, Najiah M, Alghamdi, Ghydda, Alosaimi, Wafaa, Rawas, Ghufran, Alharbi, Amaal, Tayeb, Mohammed T
Publicado 2021