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 …
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 …
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
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 …
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 …
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 …
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 …
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 …
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 …
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 …
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 …
Langerhans. They are co-secreted in response to changes in glucose concentration, and …