Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency

Author:

van Rijt Willemijn J.,Jager Emmalie A.,Allersma Derk P.,Aktuğlu Zeybek A. Çiğdem,Bhattacharya Kaustuv,Debray François-Guillaume,Ellaway Carolyn J.,Gautschi Matthias,Geraghty Michael T.,Gil-Ortega David,Larson Austin A.,Moore Francesca,Morava Eva,Morris Andrew A.,Oishi Kimihiko,Schiff Manuel,Scholl-Bürgi Sabine,Tchan Michel C.,Vockley Jerry,Witters Peter,Wortmann Saskia B.,van Spronsen Francjan,Van Hove Johan L.K.,Derks Terry G.J.ORCID

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference45 articles.

1. Chapter 103: defects of electron transfer flavoprotein and electron transfer flavoprotein-ubiquinone oxidoreductase: glutaric acidemia type II;Frerman,2014

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

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