Identifying Glucokinase Monogenic Diabetes in a Multiethnic Gestational Diabetes Mellitus Cohort: New Pregnancy Screening Criteria and Utility of HbA 1c-Reference-Cited by-同舟云学术

Identifying Glucokinase Monogenic Diabetes in a Multiethnic Gestational Diabetes Mellitus Cohort: New Pregnancy Screening Criteria and Utility of HbA 1c

Published:2015-06-24 Issue:1 Volume:39 Page:50-52
ISSN:0149-5992
Container-title:Diabetes Care
language:en
Short-container-title:Dia Care

Author:

Rudland Victoria L.,Hinchcliffe Marcus,Pinner Jason,Cole Stuart,Mercorella Belinda,Molyneaux Lynda,Constantino Maria,Yue Dennis K.,Ross Glynis P.,Wong Jencia

Funder

Sydney Medical School

National Health and Medical Research Council

Publisher

American Diabetes Association

Subject

Advanced and Specialised Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference14 articles.

1. Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.

2. Antenatal Diagnosis of Fetal Genotype Determines if Maternal Hyperglycemia Due to a Glucokinase Mutation Requires Treatment

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

4. The 0.1% of the Population With Glucokinase Monogenic Diabetes Can Be Recognized by Clinical Characteristics in Pregnancy: The Atlantic Diabetes in Pregnancy Cohort

5. Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia

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