3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinemic Hypoglycemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity-Reference-Cited by-同舟云学术

3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinemic Hypoglycemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity

Published:2009-07-01 Issue:7 Volume:94 Page:2221-2225
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Kapoor Ritika R.¹²,James Chela¹²,Flanagan Sarah E.³,Ellard Sian³,Eaton Simon¹²,Hussain Khalid¹²

Affiliation:

1. London Centre for Paediatric Endocrinology and Metabolism (R.R.K., C.J., S.Ea., K.H.), Hospital for Children National Health Service Trust, London WC1N 3JH, United Kingdom

2. The Institute of Child Health (R.R.K., C.J., S.Ea., K.H.), University College, London WC1N 1EH, United Kingdom

3. Institute of Biomedical and Clinical Science (S.E.F., S.El.), Peninsula Medical School, Exeter EX2 5DW, United Kingdom

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/94/7/2221/9062806/jcem2221.pdf

Reference22 articles.

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2. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy.;Thomas;Hum Mol Genet,1996

3. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.;Stanley;N Engl J Med,1998

4. Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome.;Kelly;J Clin Endocrinol Metab,2001

5. Protein-sensitive hypoglycemia without leucine sensitivity in hyperinsulinism caused by K(ATP) channel mutations.;Fourtner;J Pediatr,2006

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