JD Campbell, P Proks, JD Lippiat, MSP … - Diabetes, 2004 - Am Diabetes Assoc The ATP-sensitive K + channel (K ATP channel) couples glucose metabolism to
insulin secretion in pancreatic β-cells. It is comprised of sulfonylurea
receptor (SUR)-1 and Kir6.2 proteins. Binding of Mg nucleotides to the ... Cited by 8 - Related articles - BL Direct - All 4 versions
[CITATION] S Umit S, Molnes J, Molven A, Sovik O, Matschinsky F. 2003. Permanent neonatal diabetes …
DG Ramadan, MH Badawi, M Zaki, ZE Mazidi, … - Annals of Tropical Paediatrics: International Child …, 1999 - ingentaconnect.com We report nine Bedouin children from Kuwait with persistent hyperinsulinaemic
hypoglycaemia (PHHI) seen over a 13-year period in two regional hospitals. The
incidence of PHHI in this inbred community is high (1:20,000); five of them ... Cited by 5 - Related articles - BL Direct - All 4 versions
B Dekel, D Lubin, D Modan-Moses, J Quint, B … - Clinical pediatrics, 2002 - cpj.sagepub.com Co ongenital hyperinsulin- ism or persistent hyperin- sulinemic hypoglycemia of
infancy (PHHI) is character- ized by an inappropriate over- ... Departments of
1Pediatrics and 2Neonatology, Sheba Medical Center, The Sackler Faculty of ... Cited by 7 - Related articles - BL Direct - All 3 versions
E Hough, L Mair, W Mackenzie, A … - Biochemical and Biophysical Research …, 2002 - Elsevier The ATP-sensitive potassium channel is made up of four pore forming Kir6.2
subunits, surrounded by four regulatory sulphonylurea receptor (SUR) subunits.
The latter subunit contains two nucleotide-binding folds (NBFs) that confer ... Cited by 7 - Related articles - BL Direct - All 6 versions
F Reimann, H Huopio, M Dabrowski, P Proks, … - Diabetologia, 2003 - Springer Corresponding author: Dr. FM Ashcroft, University Labora- tory of Physiology,
Parks Road, Oxford, OX1 3PT UK E-mail: frances.ashcroft@physiol.ox.ac.uk
Abbreviations: CHI, Congenital hyperinsulinism; HA, haema- gluttinin; KATP, ... Cited by 15 - Related articles - BL Direct - All 7 versions
- ►endojournals.org S Tornovsky, A Crane, KE Cosgrove, K Hussain … - Journal of Clinical Endocrinology & Metabolism, 2004 - Endocrine Soc Hyperinsulinism of infancy is a genetically heterogeneous disease characterized
by dysregulation of insulin secretion resulting in severe hypoglycemia. To date,
mutations in five different genes, the sulfonylurea receptor (SUR1, ABCC8), ... Cited by 26 - Related articles - All 4 versions
[CITATION] 4th, Gonzalez G, Aguilar-Bryan L, Permutt MA & Bryan J (1996). Adenosine diphosphate as an …
AM Patch, SE Flanagan, C Boustred, AT … - Diabetes Obes Metab, 2007 - 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 9 - Related articles - All 3 versions
