D,L-3-hydroxybutyrate treatment of multiple acyl-CoA dehydrogenase deficiency (MADD)

Author:

Van Hove Johan LK,Grünewald Stephanie,Jaeken Jaak,Demaerel Philippe,Declercq Peter E,Bourdoux Pierre,Niezen-Koning Klary,Deanfeld John E,Leonard James V

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Defects of electron transfer flavoprotein and electron transfer flavoprotein-ubiquinone oxidoreductase: glutaric aciduria type II;Frerman,2001

2. Oral sodium-3-hydroxybutyrate, a novel adjunct to treatment for multiple acyl-CoA dehydrogenase deficiency;Bonham;J Inher Metab Dis,1999

3. Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy;Uziel;Pediatr Neurol,1995

4. Glutaric aciduria type II: observations in seven patients with neonatal and late-onset disease;al-Essa;J Perinatol,2000

5. The metabolism of D- and L-3-hydroxybutyrate in developing rat brain;Swiatek;Biochem Med,1984

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