Proposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency

VLCAD deficiency: Follow-up and outcome of patients diagnosed through newborn screening in Victoria

(2016) Maureen Evans et al.   MOLECULAR GENETICS AND METABOLISM

Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database

(2016) Loren D.M. Pena et al.   MOLECULAR GENETICS AND METABOLISM

Sexual dimorphism of lipid metabolism in very long-chain acyl-CoA dehydrogenase deficient (VLCAD−/−) mice in response to medium-chain triglycerides (MCT)

(2015) Sara Tucci et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

De novofatty acid biosynthesis and elongation in very long-chain acyl-CoA dehydrogenase-deficient mice supplemented with odd or even medium-chain fatty acids

(2015) Sara Tucci et al.   FEBS Journal

Fatty acid oxidation flux predicts the clinical severity of VLCAD deficiency

(2015) Eugene F. Diekman et al.   GENETICS IN MEDICINE

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

VLCAD enzyme activity determinations in newborns identified by screening: a valuable tool for risk assessment

(2011) Lars Hoffmann et al.   JOURNAL OF INHERITED METABOLIC DISEASE

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

Pre-exercise medium-chain triglyceride application prevents acylcarnitine accumulation in skeletal muscle from very-long-chain acyl-CoA-dehydrogenase-deficient mice

(2010) Sonja Primassin et al.   JOURNAL OF INHERITED METABOLIC DISEASE

The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results

(2010) Ronald J. A. Wanders et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Current issues regarding treatment of mitochondrial fatty acid oxidation disorders

(2010) Ute Spiekerkoetter et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Very long-chain acyl-CoA dehydrogenase deficiency: The effects of accidental fat loading in a patient detected through newborn screening

(2009) C. Ficicioglu et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop

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

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

(2009) Georgianne L. Arnold et al.   MOLECULAR GENETICS AND METABOLISM

Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency

(2009) Pascal Laforêt et al.   NEUROMUSCULAR DISORDERS