- ►diabetesjournals.org S Sayed, DR Langdon, S Odili, P Chen, C … - Diabetes, 2009 - Am Diabetes Assoc OBJECTIVE Heterozygous activating mutations of glucokinase have been reported to
cause hypoglycemia attributable to hyperinsulinism in a limited number of
families. We report three children with de novo glucokinase hyperinsulinism ... Cited by 3 - Related articles - All 3 versions
M Żurawek, E Wender-Ożegowska, D … - Diabetes research and clinical practice, 2007 - Elsevier Mutations in the glucokinase (GCK) and hepatocyte nuclear factor 1α (HNF1α)
gene cause maturity-onset diabetes of the young (MODY), a form of type 2
diabetes characterized by autosomal dominant mode of inheritance, early ... Cited by 5 - Related articles - All 10 versions
R Singh, ER Pearson, PM Clark, AT … - Diabetologia, 2007 - Springer Abstract Aims/hypothesis There is strong evidence that maternal diabetes while
offspring are in utero results in offspring beta cell dysfunction and diabetes
or glucose intolerance. Offspring born to mothers with a mutation in the ... Cited by 5 - Related articles - BL Direct - All 4 versions
[CITATION] Comments to:'Lindner T, Cockburn BN, Bell GI: Molecular genetics of MODY in Germany
N Shehadeh, D Bakri, PR Njolstad, R … - Diabetic Medicine, 2005 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 5 - Related articles - BL Direct - All 4 versions
- ►physiology.org B Aigner, B Rathkolb, N Herbach, MH de … - American Journal of Physiology- Endocrinology And …, 2008 - Am Physiological Soc More than 150 million people suffer from diabetes mellitus worldwide, and this
number is expected to rise substantially within the next decades. Despite its
high prevalence, the pathogenesis of diabetes mellitus is not completely ... Cited by 5 - Related articles - BL Direct - All 4 versions
[CITATION] Finding a glucokinase mutation alters patient treatment
