Permanent neonatal diabetes in an Asian infant
- 31 January 2005
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 146 (1) , 131-133
- https://doi.org/10.1016/j.jpeds.2004.09.008
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal DiabetesNew England Journal of Medicine, 2004
- Permanent Neonatal Diabetes Caused by Glucokinase DeficiencyDiabetes, 2003
- Glucokinase (GCK) mutations in hyper- and hypoglycemia: Maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancyHuman Mutation, 2003
- Transient neonatal diabetes, a disorder of imprintingJournal of Medical Genetics, 2002
- The genetic abnormality in the beta cell determines the response to an oral glucose loadDiabetologia, 2002
- Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in FranceDiabetologia, 2002
- Neonatal Diabetes Mellitus Due to Complete Glucokinase DeficiencyNew England Journal of Medicine, 2001
- Aetiopathology and genetic basis of neonatal diabetesArchives of Disease in Childhood: Fetal & Neonatal, 1997
- Body mass index reference curves for the UK, 1990.Archives of Disease in Childhood, 1995
- Linkage of type 2 diabetes to the glucokinase geneThe Lancet, 1992