Congenital Hyperinsulinism

Known as: Hypoglycemias, Persistent Hyperinsulinemic, Hyperinsulinisms, Familial, Hypoglycemias, PHHI 
A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include… (More)
National Institutes of Health

Papers overview

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Review
2011
Review
2011
Congenital hyperinsulinism (HI) is an inappropriate insulin secretion by the pancreatic β-cells secondary to various genetic… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND Congenital hyperinsulinism (CHI) is a clinically heterogeneous condition. Mutations in eight genes (ABCC8, KCNJ11… (More)
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Highly Cited
2007
Highly Cited
2007
A recent article by Jamieson in Medical Education outlined some of the (alleged) abuses of “Likert scales” with suggestions about… (More)
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Highly Cited
2006
Highly Cited
2006
Congenital hyperinsulinism of infancy (CHI) is characterized by severe hypoglycemia due to dysregulated insulin secretion… (More)
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Highly Cited
2005
Highly Cited
2005
CONTEXT Islet allografts from 2 to 4 donors can reverse type 1 diabetes. However, for islet transplants to become a widespread… (More)
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Highly Cited
2003
Highly Cited
2003
OBJECTIVE To compare the abilities and associated hypoglycemia risks of insulin glargine and human NPH insulin added to oral… (More)
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Highly Cited
2000
Highly Cited
2000
Hyperinsulinism of infancy (HI), also known as persistent hyperinsulinemic hypoglycemia of infancy, is a rare genetic disorder… (More)
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Highly Cited
2000
Highly Cited
2000
ATP-sensitive potassium channels play a major role in linking metabolic signals to the exocytosis of insulin in the pancreatic… (More)
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Highly Cited
1998
Highly Cited
1998
BACKGROUND A new form of congenital hyperinsulinism characterized by hypoglycemia and hyperammonemia was described recently. We… (More)
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Highly Cited
1998
Highly Cited
1998
The purpose of this study was to examine a young athletic population to update the data regarding epidemiology and disability… (More)
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