Sökresultat - Al-Sagheir, Afaf

A Rare Case of Adenosine Deaminase tRNA-Specific 3 Mutation, Adrenal Insufficiency, and Rhabdomyolysis av AlDhalaan, Waheeb, Syed, Faaezuddin, Javaid, Haroon A, AlSagheir, Afaf, Almustanyir, Sami

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

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Lethal digenic mutations in the K(+) channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay av Hasan, Sonia, Balobaid, Ameera, Grottesi, Alessandro, Dabbagh, Omar, Cenciarini, Marta, Rawashdeh, Rifaat, Al-Sagheir, Afaf, Bove, Cecilia, Macchioni, Lara, Pessia, Mauro, Al-Owain, Mohammed, D’Adamo, Maria Cristina

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

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

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