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Novel PTH Gene Mutations Causing Isolated Hypoparathyroidism von Hawkes, Colin R, Jubeh, Jamal M. Al, Li, Dong, Tucker, Susan E, Rajiyah, Tara, Levine, Michael A

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Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa von Al Yaarubi, Saif, Alsagheir, Afaf, Al Shidhani, Azza, Alzelaye, Somaya, Alghazir, Nadia, Brema, Imad, Alsaffar, Hussain, Al Dubayee, Mohammed, Alshahrani, Awad, Abdelmeguid, Yasmine, Omar, Omneya M, Attia, Najya, Al Amiri, Elham, Al Jubeh, Jamal, Algethami, Albandari, Alkhayyat, Haya, Haleem, Azad, Al Yahyaei, Mouza, Khochtali, Ines, Babli, Saleha, Nugud, Ahmed, Thalange, Nandu, Albalushi, Sarah, Hergli, Nadia, Deeb, Asma, Alfadhel, Majid

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