Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening-Reference-Cited by-同舟云学术

Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening

Published:2014-04 Issue:4 Volume:111 Page:484-492
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Merritt J. Lawrence,Vedal Sverre,Abdenur Jose E.,Au Sylvia M.,Barshop Bruce A.,Feuchtbaum Lisa,Harding Cary O.,Hermerath Cheryl,Lorey Fred,Sesser David E.,Thompson John D.,Yu Arthur

Funder

Health Resources and Services Administration, Maternal and Child Health Branch

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference31 articles.

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3. Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients;Vianey-Saban;Clin. Chim. Acta,1998

4. Efficiency of metabolic screening in childhood cardiomyopathies;Bonnet;Eur. Heart J.,1998

5. A young woman with persistent hypoglycemia, rhabdomyolysis, and coma: recognizing fatty acid oxidation defects in adults;Kluge;Crit. Care Med.,2003

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4. Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives;International Journal of Neonatal Screening;2023-10-06

5. Biochemical and Molecular Characteristics Among Infants with Abnormal Newborn Screen for Very-Long-Chain Acyl-Coa Dehydrogenase Deficiency: A Single Center Experience;2023