Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiency-Reference-Cited by-同舟云学术

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Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiency

Published:1996-11 Issue:1 Volume:255 Page:67-83
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Fontaine Monique,Briand Gilbert,Ser Nicole,Armelin Isabelle,Rolland Marie-Odile,Degand Pierre,Vamecq Joseph

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference32 articles.

1. Pathophysiology of peroxisomal β-oxidation;Vamecq;Essays Biochem,1989

2. Beta-oxidation of fatty acids;Schulz;Biochim Biophys Acta,1991

3. Peroxisomal lipid metabolism;Reddy;Annu Rev Nutr,1994

4. Carnitine in intermediary metabolism. The metabolism of fatty acid esters of carnitine by mitochondria;Bremer;J Biol Chem,1962

5. Long-chain carnitine acyltransferase and the role of acylcarnitine derivatives in the catalytic increase of fatty acid oxidation induced by carnitine;Fritz;J Lipid Res,1963

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1. Diabetic ketoacidosis in an adult with beta-ketothiolase deficiency (BKD) involving a novel ACAT1 variant : first report of established diabetes in BKD and a review of the literature;Clinical Diabetes and Endocrinology;2024-06-10

2. Unexplained Tachypneoa and Severe Metabolic Acidosis in a Three-Month-Old Child: A Rare Presentation of Beta-Ketothiolose Deficiency;Cureus;2022-02-05

3. Beta-Ketothiolase Deficiency;Journal of Inborn Errors of Metabolism and Screening;2016-03-30

4. Calorie Restriction and SIRT3 Trigger Global Reprogramming of the Mitochondrial Protein Acetylome;Molecular Cell;2013-01

5. A compendium of inborn errors of metabolism mapped onto the human metabolic network;Molecular BioSystems;2012

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