AT Hattersley, ER Pearson - Endocrinology, 2006 - Endocrine Soc Defining the molecular genetics of diabetes gives new insight into the
underlying etiology and so should help improve treatment. The genetic etiology
is now known for most patients with ß-cell monogenic diabetes, allowing ... Cited by 42 - Related articles - BL Direct - All 8 versions
S Ellard, K Colclough - Human mutation, 2006 - interscience.wiley.com Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes
mellitus characterized by autosomal dominant inheritance, early age of onset
(often <25 years of age), and pancreatic -cell dysfunction. MODY is both ... Cited by 32 - Related articles - BL Direct - All 4 versions
R Murphy, S Ellard, AT Hattersley - Nature Clinical Practice Endocrinology & Metabolism, 2008 - nature.com Sian Ellard is Professor of Human Molecular Genetics, Peninsula Medical School,
Exeter, UK. Following research training at the University of Swansea (UK), she
set up the Molecular Genetics Laboratory in Exeter with Professor Andrew ... Cited by 31 - Related articles - BL Direct - All 6 versions
J Holmkvist, C Cervin, V Lyssenko, W Winckler … - Diabetologia, 2006 - Springer Page 1. ARTICLE Common variants in HNF-1 α and risk of type 2 diabetes J.
Holmkvist & C. Cervin & V. Lyssenko & W. Winckler & D. Anevski ... Cited by 27 - Related articles - BL Direct - All 4 versions
- ►nih.gov S Ellard, C Bellanne-Chantelot, AT Hattersley - Diabetologia, 2008 - Springer Abstract Aims/hypothesis Mutations in the GCK and HNF1A genes are the most
common cause of the monogenic forms of diabetes known as 'maturity-onset
diabetes of the young'. GCK encodes the glucokinase enzyme, which acts as ... Cited by 16 - Related articles - BL Direct - All 11 versions
- Free from Publisher B Liljeström, T Tuomi, B Isomaa, L Sarelin, K … - Diabetes care, 2007 - Am Diabetes Assoc Mutations in the hepatocyte nuclear factor (HNF)-1α gene cause an autosomally,
dominantly inherited form of diabetes, maturity-onset diabetes of the young
(MODY) type 3, which is characterized by poor insulin secretion in response ... Cited by 1 - Related articles - BL Direct - All 6 versions
PHD MD - Am Diabetes Assoc 1 Department of Metabolic Diseases, Jagiellonian University, Medical College,
Krakow, Poland 2 Department of Internal Medicine, Diabetology and Nephrology,
Silesian School of Medicine, Zabrze, Poland 3 BioMarker Group, Kannapolis, ... Related articles
M Shepherd, PD RGN - Practical Diabetes International, 2009 - practicaldiabetesinternational.com Introduction Making a diagnosis of diabetes may be straightforward when blood
glu- cose levels reach the levels indicated by the World Health Organization
(WHO), with a fasting blood glucose ≥7.0mmol/L (126mg/dl) or two- hour ... Related articles - View as HTML - All 3 versions
Ó Rubio-Cabezas, J Argente - Journal of Pediatric Endocrinology & Metabolism, 2008 - ciberobn.es Diabetes mellitus (DM) is one of the most common chronic diseases in children
and adolescents, and type 1 DM accounts for more than 95% of cases.
Nevertheless, over the last years it has become apparent that not all cases ... Related articles - View as HTML - All 3 versions
- ►nih.gov - Free from Publisher J Skupien, S Gorczynska-Kosiorz, T Klupa, K … - Diabetes Care, 2008 - Am Diabetes Assoc OBJECTIVE—1,5-anhydroglucitol (1,5-AG) is a short-term marker of metabolic
control in diabetes. Its renal loss is stimulated in hyperglycemic conditions by
glycosuria, which results in a lowered plasma concentration. As a low renal ... Related articles - All 6 versions
