Ketone body therapy with D/L-β-hydroxybutyric acid solution in severe MADD-Reference-Cited by-同舟云学术

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Ketone body therapy with D/L-β-hydroxybutyric acid solution in severe MADD

Published:2019-09 Issue: Volume:20 Page:100491
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Fischer Tobias,Elpers Christiane,Och Ulrike,Fobker Manfred,Marquardt Thorsten

Funder

University Hospital

University of Applied Sciences

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference30 articles.

1. Electron transfer flavoprotein deficiency: functional and molecular aspects;Schiff;Mol. Genet. Metab.,2006

2. Glutaric aciduria type II: report on a previously undescribed metabolic disorder;Przyrembel;Clin. Chim. Acta,1976

3. Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts;Frerman;Proc. Natl. Acad. Sci. U. S. A.,1985

4. Defects of electron transfer flavoprotein and electron transfer flavoprotein-ubiquinone oxidoreductase: glutaric acidemia type II;Frerman,2004

5. Glutaric acidaemia type II (multiple Acyl-Coa dehydrogenation deficiency);Goodman;J. Inherit. Metab. Dis.,1984

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5. Altered nutrient status reprograms host inflammation and metabolic health via gut microbiota;The Journal of Nutritional Biochemistry;2020-06

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