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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… Expand
National Institutes of Health

Papers overview

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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… Expand
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Highly Cited
2005
Highly Cited
2005
We describe six patients (five women and one man; median age, 47 years; range, 39 to 54) with postprandial symptoms of… Expand
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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… Expand
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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… Expand
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Review
1999
Review
1999
KATP channels are a newly defined class of potassium channels based on the physical association of an ABC protein, the… Expand
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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… Expand
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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… Expand
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Highly Cited
1996
Highly Cited
1996
Adenosine triphosphate (ATP)-sensitive potassium (KATP) channels couple the cellular metabolic state to electrical activity and… Expand
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Highly Cited
1995
Highly Cited
1995
Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated… Expand
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Review
1994
Review
1994
This consensus statement of the Multi-Society Task Force summarizes current knowledge of the medical aspects of the persistent… Expand
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