Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations

Improved genetic testing for monogenic diabetes using targeted next-generation sequencing

(2013) S. Ellard et al.   DIABETOLOGIA

Diabetes Mellitus in Neonates and Infants: Genetic Heterogeneity, Clinical Approach to Diagnosis, and Therapeutic Options

(2013) Oscar Rubio-Cabezas et al.   Hormone Research in Paediatrics

Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans

(2012) Abdelhadi M Habeb et al.   ARCHIVES OF DISEASE IN CHILDHOOD

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

(2011) D. Iafusco et al.   ACTA DIABETOLOGICA

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

(2011) Abdelhadi M Habeb et al.   PEDIATRIC DIABETES

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

(2010) Kate Bennett et al.   PEDIATRIC DIABETES

Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature*

(2010) M Nuri Ozbek et al.   PEDIATRIC DIABETES

Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis

(2010) I. Garin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

6q24 transient neonatal diabetes

(2010) I. Karen Temple et al.   REVIEWS IN ENDOCRINE & METABOLIC DISORDERS

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

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

(2008) Deborah J G Mackay et al.   NATURE GENETICS