C Sempoux, Y Guiot, K Dahan, P Moulin, M … - Diabetes, 2003 - Am Diabetes Assoc Paternal mutation of ATP-sensitive K + (K ATP ) channel genes and loss of
heterozygosity (LOH) of the 11p15 region including the maternal alleles of
ABCC8, IGF2, and CDKN1C characterize the focal form of persistent ... Cited by 56 - Related articles - BL Direct - All 6 versions
- ►amjpathol.org JC Fournet, C Mayaud, P de Lonlay, MS Gross- … - American Journal of Pathology, 2001 - ASIP Congenital hyperinsulinism (CHI), previously named persistent hyperinsulinemic
hypoglycemia of infancy, is characterized by profound hypoglycemia because of
excessive insulin secretion. CHI presents as two different morphological ... Cited by 59 - Related articles - BL Direct - All 4 versions
- ►endojournals.org I Giurgea, K Laborde, G Touati, C Bellanne- … - Journal of Clinical Endocrinology & Metabolism, 2004 - Endocrine Soc Congenital hyperinsulinism (CHI) is related to two main histological pancreas
anomalies: focal adenomatous hyperplasia and diffuse ß-cell hypersecretion.
Pharmacological tests to measure acute insulin responses (AIR) to ... Cited by 33 - Related articles - BL Direct - All 4 versions
- Free from Publisher J Rahier, Y Guiot, C Sempoux - Arch Dis Child Fetal Neonatal Ed, 2000 - sur1.org The syndrome of persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI) was
de- scribed more than 40 years ago by Mc Quarrie.1 Despite the inordinate amount
of interest in this syndrome, the pathogenesis of the disease has not yet ... Cited by 66 - Related articles - View as HTML - BL Direct - All 7 versions
V Chigot, P De Lonlay, MC Nassogne, K … - Pediatric radiology, 2001 - Springer Until recently, persistent hyperinsulinemic hypoglycae- mia of infancy (PHHI)
was thought to be due to diffuse insulin hypersecretion by the pancreas called
`nesidio- blastosis'. PHHI is now known to be due to focal or dif- fuse ... Cited by 38 - Related articles - BL Direct - All 4 versions
P de Lonlay, JC Fournet, G Touati, MS Groos, … - European journal of pediatrics, 2002 - Springer P. de Lonlay (&) á G. Touati á D. Martin á C. Sevin V. Delagne á J.-M.
Saudubray á J.-J. Robert FeÂdeÂration de PeÂdiatrie, HoÃpital
Necker-Enfants-Malades, 149 rue de SeÁvres, 75743 Paris cedex 15, France ... Cited by 72 - Related articles - BL Direct - All 4 versions
- ►diabetesjournals.org [PDF] Y Tanizawa, K Matsuda, M Matsuo, Y Ohta, N … - Diabetes, 2000 - Am Diabetes Assoc To elucidate the genetic etiology of persistent hyperin- sulinemic hypoglycemia
of infancy (PHHI) in the Japan- ese population, we conducted a polymerase chain
reac- tion–single-strand conformation polymorphism analy- sis of the ... Cited by 33 - Related articles - BL Direct - All 3 versions
F Menni, P de Lonlay, C Sevin, G Touati, C … - Pediatrics, 2001 - Am Acad Pediatrics Methods. The neurologic development of 90 PHHI patients was studied
retrospectively. Sixty-three patients were treated surgically and 27 were
treated medically. Fifty-four patients were neonates, of whom 8 were ... Cited by 108 - Related articles - BL Direct - All 6 versions
A Goossens, W Gepts, JM Saudubray, JP … - The American Journal of Surgical Pathology, 1989 - journals.lww.com The American Journal of Surgical Pathology 13(9): 766-775, 1989 1989 Raven
Press, Ltd., New York Diffuse and Focal Nesidioblastosis A Clinicopathological
Study of 24 Patients with Persistent Neonatal Hyperinsulinemic Hypoglycemia ... Cited by 103 - Related articles - All 4 versions
- ►endojournals.org C Sempoux, Y Guiot, A Lefevre, C Nihoul- … - Journal of Clinical Endocrinology & Metabolism, 1998 - Endocrine Soc The two major forms of infantile persistent hyperinsulinemic hypoglycemia
require different treatments, but are difficult to differentiate during surgery.
Indeed, one is characterized by focal adenomatous hyperplasia often ... Cited by 65 - Related articles - BL Direct - All 4 versions
