Review on monogenic diabetes

Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

(2010) Trine W Boesgaard et al.   BMC Medical Genetics

Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitus

(2010) RJ Gardner et al.   CLINICAL GENETICS

Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

(2010) K. R. Owen et al.   DIABETES CARE

Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY)

(2009) A. L. Cuesta-Munoz et al.   DIABETES CARE

Maturity-Onset Diabetes of the Young in Children With Incidental Hyperglycemia:: A multicenter Italian study of 172 families

(2009) R. Lorini et al.   DIABETES CARE

Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype

(2009) Alessia Cappelli et al.   DIABETES RESEARCH AND CLINICAL PRACTICE

Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish population

(2009) Jesús Solera et al.   DIABETES RESEARCH AND CLINICAL PRACTICE

Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes

(2009) O. Rubio-Cabezas et al.   DIABETIC MEDICINE

A genetic diagnosis ofHNF1Adiabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients

(2009) M. Shepherd et al.   DIABETIC MEDICINE

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

The KATP Channel and Neonatal Diabetes

(2009) Kenju SHIMOMURA   ENDOCRINE JOURNAL

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

(2009) Janniche Torsvik et al.   HUMAN GENETICS

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia

(2009) Kara K. Osbak et al.   HUMAN MUTATION

MODY7Gene,KLF11, Is a Novel p300-dependent Regulator ofPdx-1(MODY4) Transcription in Pancreatic Islet β Cells

(2009) Martin E. Fernandez-Zapico et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The diagnosis and management of monogenic diabetes in children and adolescents

(2009) Andrew Hattersley et al.   PEDIATRIC DIABETES

Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes Register

(2009) Barbara Wiedemann et al.   PEDIATRIC DIABETES

Mutations at the BLK locus linked to maturity onset diabetes of the young and  -cell dysfunction

(2009) M. Borowiec et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Heterozygous Missense Mutations in the Insulin Gene Are Linked to Permanent Diabetes Appearing in the Neonatal Period or in Early Infancy: A Report From the French ND (Neonatal Diabetes) Study Group

(2008) M. Polak et al.   DIABETES

Neurological Features and Enzyme Therapy in Patients With Endocrine and Exocrine Pancreas Dysfunction Due to CEL Mutations

(2008) M. Vesterhus et al.   DIABETES CARE

Insulin Gene Mutations as Cause of Diabetes in Children Negative for Five Type 1 Diabetes Autoantibodies

(2008) R. Bonfanti et al.   DIABETES CARE

Pregnancy outcome in patients with raised blood glucose due to a heterozygous glucokinase gene mutation

(2008) G. Spyer et al.   DIABETIC MEDICINE

Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young

(2008) S. Ellard et al.   DIABETOLOGIA

Neonatal Diabetes Mellitus

(2008) Lydia Aguilar-Bryan et al.   ENDOCRINE REVIEWS

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

Diagnosis and treatment of neonatal diabetes: an United States experience†

(2008) Julie Støy et al.   PEDIATRIC DIABETES

Clinical implications of a molecular genetic classification of monogenic β-cell diabetes

(2008) Rinki Murphy et al.   Nature clinical practice. Endocrinology & metabolism

The G53D Mutation in Kir6.2 (KCNJ11) Is Associated with Neonatal Diabetes and Motor Dysfunction in Adulthood that Is Improved with Sulfonylurea Therapy

(2007) Joseph C. Koster et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM