Clinical outcome, biochemical and therapeutic follow-up in 14 Austrian patients with Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency (LCHADD)

Development and pathomechanisms of cardiomyopathy in very long-chain acyl-CoA dehydrogenase deficient (VLCAD−/−) mice

(2014) Sara Tucci et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Effect of Feeding, Exercise, and Genotype on Plasma 3-Hydroxyacylcarnitines in Children With LCHAD Deficiency

(2013) Melanie B. Gillingham et al.   TOPICS IN CLINICAL NUTRITION

Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients

(2012) Julien Baruteau et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Refined Staging for Chorioretinopathy in Long-Chain 3-Hydroxyacyl Coenzyme A Dehydrogenase Deficiency

(2012) Tiina Tyni et al.   OPHTHALMIC RESEARCH

Substrate oxidation and cardiac performance during exercise in disorders of long chain fatty acid oxidation

(2011) Annie M. Behrend et al.   MOLECULAR GENETICS AND METABOLISM

Outcome in six patients with mitochondrial trifunctional protein disorders identified by newborn screening

(2010) Astrid Sperk et al.   MOLECULAR GENETICS AND METABOLISM

Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop

(2009) U. Spiekerkoetter et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Carnitine palmitoyltransferase II deficiency: Successful anaplerotic diet therapy

(2008) C. R. Roe et al.   NEUROLOGY