Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012

GCK-MODY in the US National Monogenic Diabetes Registry: frequently misdiagnosed and unnecessarily treated

(2016) David Carmody et al.   ACTA DIABETOLOGICA

Clinical and molecular characterization of a novel INS mutation identified in patients with MODY phenotype

(2016) Barbara Piccini et al.   European Journal of Medical Genetics

Survey on etiological diagnosis of diabetes in 1244 Italian diabetic children and adolescents: Impact of access to genetic testing

(2015) Enza Mozzillo et al.   DIABETES RESEARCH AND CLINICAL PRACTICE

Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohort

(2015) S. Bacon et al.   DIABETIC MEDICINE

A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2

(2014) Enza Mozzillo et al.   BMC Medical Genetics

No Sign of Proliferative Retinopathy in 15 Patients With Permanent Neonatal Diabetes With a Median Diabetes Duration of 24 Years

(2014) Dario Iafusco et al.   DIABETES CARE

Treatment of young patients with HNF1A mutations (HNF1A-MODY)

(2014) K. Raile et al.   DIABETIC MEDICINE

Prevalence of Vascular Complications Among Patients With Glucokinase Mutations and Prolonged, Mild Hyperglycemia

(2014) Anna M. Steele et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Definition, epidemiology, and classification of diabetes in children and adolescents

(2014) Maria E Craig et al.   PEDIATRIC DIABETES

Type 2 diabetes in the child and adolescent

(2014) Phil Zeitler et al.   PEDIATRIC DIABETES

The diagnosis and management of monogenic diabetes in children and adolescents

(2014) Oscar Rubio-Cabezas et al.   PEDIATRIC DIABETES

Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR?

(2013) Valeria Grasso et al.   ACTA DIABETOLOGICA

Prevalence of Diabetes in U.S. Youth in 2009: The SEARCH for Diabetes in Youth Study

(2013) D. J. Pettitt et al.   DIABETES CARE

Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

(2013) H. U. Irgens et al.   DIABETOLOGIA

Prevalence, Characteristics and Clinical Diagnosis of Maturity Onset Diabetes of the Young Due to Mutations in HNF1A, HNF4A, and Glucokinase: Results From the SEARCH for Diabetes in Youth

(2013) Catherine Pihoker et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Thiamine responsive megaloblastic anemia: a novelSLC19A2compound heterozygous mutation in two siblings

(2013) Enza Mozzillo et al.   PEDIATRIC DIABETES

Systematic Assessment of Etiology in Adults With a Clinical Diagnosis of Young-Onset Type 2 Diabetes Is a Successful Strategy for Identifying Maturity-Onset Diabetes of the Young

(2012) G. Thanabalasingham et al.   DIABETES CARE

Prevalence of monogenic diabetes amongst Polish children after a nationwide genetic screening campaign

(2012) W. Fendler et al.   DIABETOLOGIA

MODY

(2011) Stefan S. Fajans et al.   DIABETES CARE

Reclassification of diabetes type in pediatric patients initially classified as type 2 diabetes mellitus: 15 years follow-up using routine data from the German/Austrian DPV database

(2011) W.L. Awa et al.   DIABETES RESEARCH AND CLINICAL PRACTICE

Management of diabetes mellitus in infants

(2011) Beate Karges et al.   Nature Reviews Endocrinology

Maturity-onset diabetes of the young (MODY): how many cases are we missing?

(2010) B. M. Shields et al.   DIABETOLOGIA

Epidemiology of Type 1 Diabetes

(2010) David M. Maahs et al.   ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA

Phenotypical aspects of maturity-onset diabetes of the young (MODY diabetes) in comparison with Type 2 diabetes mellitus (T2DM) in children and adolescents: experience from a large multicentre database

(2009) E. Schober et al.   DIABETIC MEDICINE

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations

(2008) Sara E. Pinney et al.   JOURNAL OF CLINICAL INVESTIGATION