A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis

por AlDhalaan, Waheeb, Syed, Faaezuddin, Javaid, Haroon A, AlSagheir, Afaf, Almustanyir, Sami
Publicado 2021

25-Hydroxylase vitamin D deficiency in 27 Saudi Arabian subjects: a clinical and molecular report on CYP2R1 mutations

por Bakhamis, Sarah, Imtiaz, Faiqa, Ramzan, Khushnooda, De Vol, Edward, Al-Sagheir, Osamah, Al-Rajhi, Abdulrahman, Alashwal, Abdullah, Bin Abbas, Bassam, Sakati, Nadia, Al-Sagheir, Afaf
Publicado 2021

Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries

por Al Juraibah, Fahad, Al Amiri, Elham, Al Dubayee, Mohammed, Al Jubeh, Jamal, Al Kandari, Hessa, Al Sagheir, Afaf, Al Shaikh, Adnan, Beshyah, Salem A., Deeb, Asma, Habeb, Abdelhadi, Mustafa, Manal, Zidan, Hanaa, Mughal, M. Zulf
Publicado 2021

Outcome of COVID19 in Patients With Osteogenesis Imperfecta: A Retrospective Multicenter Study in Saudi Arabia

por Alshukairi, Abeer N., Doar, Hazem, Al-Sagheir, Afaf, Bahasan, Mona A., Sultan, Anas A., Al Hroub, Mohammad K., Itani, Dina, Khalid, Imran, Saeedi, Mohammed F., Bakhamis, Sarah, Layqah, Laila, Almutairi, Afnan A., Saifullah, Mona, Hefni, Lama, Al-Omari, Awad, Alraddadi, Basem M., Baharoon, Salim A.
Publicado 2022