Genetic mutations associated with neonatal diabetes mellitus in Omani patients

The effect of early, comprehensive genomic testing on clinical care in neonatal diabetes: an international cohort study

(2015) Elisa De Franco et al.   LANCET

A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins

(2015) Adriana Mangue Esquiaveto-Aun et al.   Diabetology & Metabolic Syndrome

SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion

(2012) F. H. Sansbury et al.   DIABETOLOGIA

Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births

(2011) D. Iafusco et al.   ACTA DIABETOLOGICA

Neonatal Diabetes: An Expanding List of Genes Allows for Improved Diagnosis and Treatment

(2011) Siri Atma W. Greeley et al.   Current Diabetes Reports

Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia

(2011) Abdelhadi M Habeb et al.   PEDIATRIC DIABETES

Genetics and pathophysiology of neonatal diabetes mellitus

(2011) Rochelle N Naylor et al.   Journal of Diabetes Investigation

Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene

(2010) Kate Bennett et al.   PEDIATRIC DIABETES

Muscle Dysfunction Caused by a KATP Channel Mutation in Neonatal Diabetes Is Neuronal in Origin

(2010) R. H. Clark et al.   SCIENCE

Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births

(2009) A. S. Slingerland et al.   DIABETOLOGIA

Wolcott-Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families

(2009) Oscar Rubio-Cabezas et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM