Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports

por Ismail, Mariam M., Musa, Salwa A., Hassan, Samar S., Abdullah, Mohamed A.
Publicado 2023

THU232 Genetic Study In A Series Of 29 Triple A Syndrome Patients From 19 Sudanese Families - Identification Of Two Novel AAAS Mutations

por Koehler, Katrin, Quitter, Friederike, Landgraf, Dana, Streiff, Eliane, Abdullah, Mohamed A, Hassan, Samar S, Huebner, Angela, Musa, Salwa A
Publicado 2023

Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children

por Musa, Salwa A., Ibrahim, Areej A., Hassan, Samar S., Johnson, Matthew B, Basheer, Asmahan T., Arabi, Ali M., Abdullah, Mohamed A.
Publicado 2020

Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village…

por Rowlands, Amanda, Deeb, Asma, Ladjouze, Asmahane, Hamza, Rasha T, Musa, Salwa A, Raza, Jamal, Jennane, Farida, Abu-Libdeh, Abdulsalam, Chanoine, Jean-Pierre
Publicado 2021