A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1 von Huneif, Mohammed Ayed, Alhazmy, Ziyad Hamad, Shoomi, Anas M., Alghofely, Mohammed A., Heena, Humariya, Mushiba, Aziza M., AlSaheel, Abdulhamid

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3M Syndrome: An Easily Recognizable yet Underdiagnosed Cause of Proportionate Short Stature von Al-Dosari, Mohammed S., PhD, Al-Shammari, Muneera, MD, Shaheen, Ranad, PhD, Faqeih, Eissa, MD, AlGhofely, Mohammed A., MD, Boukai, Ahmad, MD, Alkuraya, Fowzan S., MD

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Association of HLA‐DR‐DQ alleles, haplotypes, and diplotypes with type 1 diabetes in Saudis von Eltayeb‐Elsheikh, Nezar, Khalil, Eltahir, Mubasher, Mohamed, AlJurayyan, Abdullah, AlHarthi, Hanan, Omer, Waleed H., Elghazali, Inas, Sherbeeni, Suphia M., Alghofely, Mohammed A., Ilonen, Jorma, Elghazali, Gehad

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Epilepsy in patients with insulin-dependent diabetes and relation to glutamic acid decarboxylase 65 von Mahmoud, Adel A, Abdelmagid, Tayseer, AlGhofely, Mohammed, Hamed, Ahmed M, Al Sharif, Roaa

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Isolated cortisol deficiency: a rare cause of neonatal cholestasis von Al-Hussaini, Abdulrahman, Almutairi, Awatif, Mursi, Alaaddin, Alghofely, Mohammed, Asery, Ali

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