• Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation
• Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt
• Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience
• Co-opting regulation bypass repair as a gene-correction strategy for monogenic diseases
• Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database
• Ethnic variation and structure-function analysis of tauopathy-associated <em>PERK</em> alleles
• Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center
• Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience
• Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India
• Identification of Two Novel Compound Heterozygous <em>EIF2AK3</em> Mutations Underlying Wolcott-Rallison Syndrome in a Chinese Family
• Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott-Rallison Syndrome in a Chinese Family
• Kidney biopsy findings in children with diabetes mellitus
• Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 gene
• Long-term follow-up of a child with Wolcott-Rallison syndrome
• Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study
• Neonatal Diabetes Mellitus: Novel Mutations
• PERK inhibition in zebrafish mimics human Wolcott-Rallison syndrome phenotypes
• PERK participates in cardiac valve development via fatty acid oxidation and endocardial-mesenchymal transformation
• Recurrent Liver Failure Due to Wolcott Rallison Syndrome
• The first presentation of Wolcott-Rallison syndrome in a four-month-old infant with diabetic ketoacidosis (DKA) precipitating by COVID-19: A case report
• Wolcott-Rallison Syndrome Affecting Three Consecutive Conceptions of a Consanguineous Couple
• Wolcott-Rallison Syndrome, a Rare Cause of Permanent Diabetes Mellitus in Infants-Case Report
• Wolcott-Rallison syndrome: a case series of three patients