Primary Hypothyroidism with Pituitary Hyperplasia in an Omani Girl

por Abdallah Fadle, Wafa, Al Reesi, Ali, Al-Shabibi, Saud, Khamis Al-Badi, Maryam
Publicado 2022

Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia

por Willows, Jamie, Al Badi, Maryam, Richardson, Chloe, Al Sinani, Aisha, Edwards, Noel, Rice, Sarah, Sayer, John A.
Publicado 2019

Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy: A one-decade single-center experience

por Al-Badi, Maryam K., Al-Azkawi, Hanan S., Al-Yahyaei, Mouza S., Mula-Abed, Waad A., Al-Senani, Aisha M.
Publicado 2019

A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population

por Alzahrani, Ali S, Alswailem, Meshael, Abbas, Bassam Bin, Qasem, Ebtesam, Alsagheir, Afaf, Al Shidhani, Azza, Al Sinani, Aisha, Al Badi, Maryam, Al-Maqbali, Ali, Al Shawi, Manal, Albunyan, Abdulhameed, Bin Nafisah, Abdulghani, Shi, Yufei
Publicado 2021