Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children-Reference-Cited by-同舟云学术

Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children

Published:2014-07-29 Issue:3 Volume:38 Page:489-493
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Brown Laurie M.,Corrado Michelle M.,van der Ende Rixt M.,Derks Terry G. J.,Chen Margaret A.,Siegel Sara,Hoyt Kate,Correia Catherine E.,Lumpkin Christopher,Flanagan Theresa B.,Carreras Caroline T.,Weinstein David A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-014-9744-1

Reference21 articles.

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2. Bachrach BE, Weinstein DA, Orho-Melander M, Burgess A, Wolfsdorf JI (2002) Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations. J Pediatr 140:781–783

3. Bashan N, Potashnik R, Ehrlich T, Moses SW (1987) Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX. J Inherit Metab Dis 10(2):119–127

4. Bodamer OA, Hussein K, Morris AA et al (2006) Glucose and leucine kinetics in idiopathic ketotic hypoglycemia. Arch Dis Child 91:483–486

5. Daly LP, Osterhoudt KC, Weinzimer SA (2003) Presenting features of idiopathic ketotic hypoglycemia. J Emerg Med 25:39–43

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