G Klöppel, M Anlauf - Pathology Case Reviews, 2006 - journals.lww.com The endocrine tumors of the pancreas are composed of cells with a neuroendocrine
phenotype. Well-differentiated tumors, well-differentiated carcinomas, poorly
differentiated carcinomas, functioning (insulinomas, gastrinomas, ... Cited by 135 - Related articles - BL Direct - All 4 versions
- ►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
- ►shouxi.net T Otonkoski, K Näntö-Salonen, M Seppänen, … - Diabetes, 2006 - Am Diabetes Assoc Congenital hyperinsulinism of infancy (CHI) is characterized by severe
hypoglycemia due to dysregulated insulin secretion, associated with either focal
or diffuse pathology of the endocrine pancreas. The focal condition is ... Cited by 77 - Related articles - BL Direct - All 7 versions
- ►physiology.org H Huopio, SL Shyng, T Otonkoski, CG Nichols - American Journal of Physiology- Endocrinology And …, 2002 - Am Physiological Soc ATP-sensitive potassium (K ATP ) channels are inhibited by intracellular ATP and
activated by ADP. Nutrient oxidation in -cells leads to a rise in [ATP]-to-[ADP]
ratios, which in turn leads to reduced K ATP channel activity, ... Cited by 61 - Related articles - BL Direct - All 6 versions
- ►endojournals.org SJ Marx, WF Simonds - Endocrine reviews, 2005 - Endocrine Soc Hereditary origin of a tumor helps toward early discovery of its mutated gene;
for example, it supports the compilation of a DNA panel from index cases to
identify that gene by finding mutations in it. The gene for a hereditary ... Cited by 41 - Related articles - BL Direct - All 5 versions
M Anlauf, D Wieben, A Perren, B Sipos, P … - The American journal of surgical pathology, 2005 - journals.lww.com Abstract: Persistent hyperinsulinemic hypoglycemia (PHH) in adults that is not
caused by an insulinoma is a rare and not well- characterized disease that has
been named nesidioblastosis. In this study, we defined and scrutinized ... Cited by 41 - Related articles - All 5 versions
DD De León, CA Stanley - Nature Clinical Practice Endocrinology & Metabolism, 2007 - nature.com Diva D De León is an Assistant Professor of Pediatrics at the University of
Pennsylvania, Philadelphia, PA, USA, and an Attending Physician in the Division
of Endocrinology, The Children's Hospital of Philadelphia. Her research ... Cited by 28 - Related articles - BL Direct - 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 IA Leclercq, C Sempoux, P Starkel, Y … - British Medical Journal, 2006 - gut.bmj.com Results: When introduced after two weeks of CCl 4 , pioglitazone reduced hepatic
fibrosis, OH proline content, hepatic mRNA expression of collagen type I, and
profibrotic genes, as well as the number of activated smooth muscle actin ... Cited by 21 - Related articles - BL Direct - All 6 versions
