ABCC8-Related Maturity-Onset Diabetes of the Young (MODY12): Clinical Features and Treatment Perspective

Practical Aspects of Monogenic Diabetes: A Clinical Point of View

(2016) Carl-Hugo Lachance   Canadian Journal of Diabetes

ABCC8R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes

(2015) Leslie J. Baier et al.   DIABETES

Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations

(2015) Jacques Beltrand et al.   DIABETES CARE

Long-term Glycemic Variability and Risk of Adverse Outcomes: A Systematic Review and Meta-analysis

(2015) Catherine Gorst et al.   DIABETES CARE

Effects of luseogliflozin, a sodium-glucose co-transporter 2 inhibitor, on 24-h glucose variability assessed by continuous glucose monitoring in Japanese patients with type 2 diabetes mellitus: a randomized, double-blind, placebo-controlled, crossover stu

(2015) R. Nishimura et al.   DIABETES OBESITY & METABOLISM

Low Prevalence ofHNF1AMutations After Molecular Screening of Multiple MODY Genes in 58 Italian Families Recruited in the Pediatric or Adult Diabetes Clinic From a Single Italian Hospital: Table 1

(2014) Maurizio Delvecchio et al.   DIABETES CARE

Exploring the Potential of the SGLT2 Inhibitor Dapagliflozin in Type 1 Diabetes: A Randomized, Double-Blind, Placebo-Controlled Pilot Study

(2014) Robert R. Henry et al.   DIABETES CARE

ABCC8 genetic variants and risk of diabetes mellitus

(2014) Polin Haghverdizadeh et al.   GENE

The diagnosis and management of monogenic diabetes in children and adolescents

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

Glucose Variability

(2013) F. J. Service   DIABETES

De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed

(2013) Juraj Stanik 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

Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study

(2013) Kanetee Busiah et al.   Lancet Diabetes & Endocrinology

Maturity onset diabetes of the young: identification and diagnosis

(2013) T. J. McDonald et al.   ANNALS OF CLINICAL BIOCHEMISTRY

Sulfonylurea Receptor 1 in Central Nervous System Injury: A Focused Review

(2012) J Marc Simard et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene

(2012) Amélie Bonnefond et al.   PLoS One

Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations

(2011) J.-P. Riveline et al.   DIABETES CARE

MODY

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

Normal Reference Range for Mean Tissue Glucose and Glycemic Variability Derived from Continuous Glucose Monitoring for Subjects Without Diabetes in Different Ethnic Groups

(2011) Nathan R. Hill et al.   Diabetes Technology & Therapeutics

Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations

(2011) Lucie Gonsorcikova et al.   PEDIATRIC DIABETES

Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation

(2010) N. Zwaveling-Soonawala et al.   DIABETOLOGIA

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

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