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Hormone Research in Paediatrics|February 10, 2015
Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohortAbdelhadi M Habeb, Asma Deeb, Matthew Johnson, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|January 17, 2024
Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up studyDenise Aldrian, Clemens Bochdansky, Anna M Kavallar, et al.
Diabetes|February 27, 2026
Biallelic Pathogenic Variants in IL2RA Cause Neonatal-Onset Monogenic Autoimmune DiabetesGeorgia Bonfield, James Russ-Silsby, Suraj Ramchand, et al.
European Journal of Endocrinology|October 15, 2020
Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivityEmily Cottrell, Claudia P Cabrera, Miho Ishida, et al.
Pediatric Diabetes|November 15, 2021
Efficacy and safety of the addition of sitagliptin to treatment of youth with type 2 diabetes and inadequate glycemic control on metformin without or with insulinMuhammad Yazid Jalaludin, Asma Deeb, Philip Zeitler, et al.
Journal of the American Society of Nephrology : JASN|December 16, 2017
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1Sven Enerbäck, Daniel Nilsson, Noel Edwards, et al.
Pediatric Diabetes|November 15, 2021
A randomized clinical trial of the efficacy and safety of sitagliptin as initial oral therapy in youth with type 2 diabetesR Ravi Shankar, Philip Zeitler, Asma Deeb, 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.
American Journal of Human Genetics|April 23, 2019
A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological DevelopmentElisa De Franco, Rachel A Watson, Wolfgang J Weninger, et al.
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