Associated Papers
Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.
Mianesaz H et al.
Journal of Diabetes Investigation, 2024
Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.
Aldrian D et al.
Liver International : Official Journal of the International Association for the Study of the Liver, 2024
38230874 (PubMed )
Supplement: supplement_1.pdf
Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates.
Deeb A et al.
American Journal of Medical Genetics. Part A, 2016
Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.
Habeb AM et al.
Hormone Research in Paediatrics, 2015
Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.
Habeb AM
The Libyan Journal of Medicine, 2013
Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature.
Ozbek MN et al.
Pediatric Diabetes, 2010
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