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BMJ Case Reports|February 10, 2023
Two siblings with a rare type of maturity-onset diabetes of the young (MODY)Fatima Riyadh Alhakim, Haya AlKhayyatMolecular Cytogenetics|December 17, 2022
Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case reportYousif Khalifa, Hisham Y Hassan, Anja Weise, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2007
Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemiaHaya Alkhayyat, Henrik B T Christesen, James Steer, et al.Cureus|December 22, 2025
Aldosterone Synthase Deficiency Type I in a Neonate: Diagnostic, Genetic, and Therapeutic Insights From a Novel CYP11B2 VariantHaydy M Khalifa, Rayan H Mohamed, Hisham Y Hassan, et al.American Journal of Medical Genetics. Part A|November 10, 2005
Costello syndrome and hyperinsulinemic hypoglycemiaSaji Alexander, Dina Ramadan, Haya Alkhayyat, et al.Diabetes Research and Clinical Practice|January 25, 2021
Use of ambulatory glucose monitoring and analysis of ambulatory glucose profile in clinical practice for diabetes management; a position statement of the Arab Society of Paediatric Endocrinology and diabetesAsma Deeb, Tawfik Muammar, Hussain Alsaffar, et al.Clinical Medicine Insights. Endocrinology and Diabetes|October 23, 2023
Lessons Learned From COVID-19 Lockdown: An ASPED/MENA Study on Lifestyle Changes and Quality of Life During Ramadan Fasting in Children and Adolescents Living With Type 1 DiabetesAmir Babiker, Nancy Samir Elbarbary, Bothainah Alaqeel, et al.Orphanet Journal of Rare Diseases|March 14, 2024
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North AfricaSaif Al Yaarubi, Afaf Alsagheir, Azza Al Shidhani, et al.Hormone Research in Paediatrics|November 21, 2017
An International Consortium Update: Pathophysiology, Diagnosis, and Treatment of Polycystic Ovarian Syndrome in AdolescenceLourdes Ibáñez, Sharon E Oberfield, Selma Witchel, et al.Pageof 1