- ►physiology.org MJ Dunne, KE Cosgrove, RM Shepherd, A … - Physiological reviews, 2004 - Am Physiological Soc The earliest description of hyperinsulinism appears to have been that provided
by Laidlaw in 1938 who used the term nesidioblastosis to describe the severe,
recurrent hypoglycemia associated with an inappropriate elevation of serum ... Cited by 108 - Related articles - BL Direct - All 3 versions
I Franklin, J Gromada, A Gjinovci, S … - Diabetes, 2005 - Am Diabetes Assoc Glucagon, secreted from islet α-cells, mobilizes liver glucose. During
hyperglycemia, glucagon secretion is inhibited by paracrine factors from other
islet cells, but in type 1 and type 2 diabetic patients, this suppression ... Cited by 74 - Related articles - All 4 versions
ME Patti, G McMahon, EC Mun, A Bitton, JJ … - Diabetologia, 2005 - Springer Page 1. Diabetologia (2005) 48: 2236–2240 DOI 10.1007/s00125-005-1933-x SHORT
COMMUNICATION ME Patti . G. McMahon . EC Mun . A. Bitton . JJ Holst . ... Cited by 71 - Related articles - BL Direct - All 3 versions
- ►endojournals.org J Gromada, I Franklin, CB Wollheim - Endocrine reviews, 2007 - Endocrine Soc Glucagon, a hormone secreted from the -cells of the endocrine pancreas, is
critical for blood glucose homeostasis. It is the major counterpart to insulin
and is released during hypoglycemia to induce hepatic glucose output. The ... Cited by 60 - Related articles - BL Direct - All 4 versions
K Hųjlund, T Hansen, M Lajer, JE Henriksen, … - Diabetes, 2004 - Am Diabetes Assoc Recently, various subtypes of familial hyperinsulinemic hypoglycemia with an
autosomal-dominant inheritance have been etiologically characterized. In the
present study, we have delineated the genetics and metabolic phenotype of a ... Cited by 29 - Related articles - BL Direct - All 5 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
I Giurgea, C Bellanné-Chantelot, M Ribeiro, L … - Horm Res, 2006 - content.karger.com Congenital hyperinsulinism (CHI), characterized by profound hypoglycaemia
related to inappropriate insulin secretion, may be associated histologically
with either diffuse insulin hypersecretion or focal adenomatous ... Cited by 21 - Related articles - BL Direct - All 5 versions
- ►nih.gov T Otonkoski, H Jiao, N Kaminen-Ahola, I Tapia- … - The American Journal of Human Genetics, 2007 - Elsevier Exercise-induced hyperinsulinism (EIHI) is a dominantly inherited hypoglycemic
disorder characterized by inappropriate insulin secretion during anaerobic
exercise or on pyruvate load. We aimed to identify the molecular basis of ... Cited by 20 - Related articles - BL Direct - All 12 versions
P Lonlay, I Giurgea, C Sempoux, G Touati, F … - Journal of inherited metabolic disease, 2005 - Springer Page 1. Dominantly inherited hyperinsulinaemic hypoglycaemia P. de Lonlay 1* ,
I. Giurgea 1 , C. Sempoux 4 , G. Touati 1 , F. Jaubert 1 , ... Cited by 16 - Related articles - All 5 versions
K Hussain - Horm Res, 2008 - content.karger.com Hyperinsulinaemic hypoglycaemia is a cause of persistent hypoglycaemia in the
neonatal and infancy periods. Prompt recognition and management of patients with
hyperinsulinaemic hypoglycaemia are essential, if brain damage and ... Cited by 12 - Related articles - BL Direct - All 5 versions
