Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds

M Cornblath, JM Hawdon, AF Williams… - …, 2000 - publications.aap.org
The definition of clinically significant hypoglycemia remains one of the most confused and
contentious issues in contemporary neonatology. In this article, some of the reasons for …

Hyperinsulinism in infancy: from basic science to clinical disease

MJ Dunne, KE Cosgrove, RM Shepherd… - Physiological …, 2004 - journals.physiology.org
Dunne, Mark J., Karen E. Cosgrove, Ruth M. Shepherd, Albert Aynsley-Green, and Keith J.
Lindley. Hyperinsulinism in Infancy: From Basic Science to Clinical Disease. Physiol Rev 84 …

Medical, statistical, ethical and human rights considerations in the assessment of age in children and young people subject to immigration control

A Aynsley-Green, TJ Cole, H Crawley… - British medical …, 2012 - academic.oup.com
Background Unprecedented changes in both the scale and the complexity of international
migration have led to international concern and controversy over the assessment of age in …

[HTML][HTML] Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

PT Clayton, S Eaton, A Aynsley-Green… - The Journal of …, 2001 - Am Soc Clin Investig
A female infant of nonconsanguineous Indian parents presented at 4 months with a
hypoglycemic convulsion. Further episodes of hypoketotic hypoglycemia were associated …

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

M Bitner-Glindzicz, KJ Lindley, P Rutland, D Blaydon… - Nature …, 2000 - nature.com
Usher syndrome type 1 describes the association of profound, congenital sensorineural
deafness, vestibular hypofunction and childhood onset retinitis pigmentosa 1. It is an …

[HTML][HTML] Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor

MJ Dunne, C Kane, RM Shepherd… - … England Journal of …, 1997 - Mass Medical Soc
Persistent hyperinsulinemic hypoglycemia of infancy is caused by inappropriate and
excessive secretion of insulin. Although the disease is rare in outbred communities …

Loss of functional KATP channels in pancreatic β–cells causes persistent hyperinsulinemic hypoglycemia of infancy

C Kane, RM Shepherd, PE Squires, PRV Johnson… - Nature medicine, 1996 - nature.com
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a disorder of childhood
associated with inappropriate hypersecretion of insulin by the pancreas. The pathogenesis …

Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.

M Orho, NU Bosshard, NR Buist… - The Journal of …, 1998 - Am Soc Clin Investig
Glycogen storage disease type 0 (GSD-0) is a rare form of fasting hypoglycemia presenting
in infancy or early childhood and accompanied by high blood ketones and low alanine and …

Hypoglycemia in infancy: the need for a rational definition

A Ciba Foundation Discussion Meeting… - …, 1990 - publications.aap.org
A discussion meeting was held on October 17, 1989, to address the current status of the
definition of significant hypoglycemia in infancy, especially in the normal-and low-birth …

[HTML][HTML] Glucose regulates islet amyloid polypeptide gene transcription in a PDX1-and calcium-dependent manner

WM Macfarlane, SC Campbell, LJ Elrick… - Journal of Biological …, 2000 - ASBMB
Islet amyloid polypeptide (IAPP) and insulin are expressed in the β-cells of the islets of
Langerhans. They are co-secreted in response to changes in glucose concentration, and …