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

Déficit en acyl-CoA-déshydrogénase des acides gras à chaîne moyenne (MCAD) : consensus français pour le dépistage, le diagnostic, et la prise en charge

(2012) F. Feillet et al.   ARCHIVES DE PEDIATRIE

Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany *

(2011) Martin Lindner et al.   Orphanet Journal of Rare Diseases

Fasting-induced oxidative stress in very long chain acyl-CoA dehydrogenase-deficient mice

(2010) Sara Tucci et al.   FEBS Journal

Fatty acid oxidation disorders: outcome and long-term prognosis

(2010) Bridget Wilcken   JOURNAL OF INHERITED METABOLIC DISEASE

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

Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years

(2009) B. Wilcken et al.   PEDIATRICS

Newborn screening for medium chain acyl CoA dehydrogenase deficiency

(2008) J V Leonard et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Disturbed hepatic carbohydrate management during high metabolic demand in medium-chain acyl-CoA dehydrogenase (MCAD)-deficient mice

(2008) Hilde Herrema et al.   HEPATOLOGY

Mitochondrial fatty acid oxidation defects—remaining challenges

(2008) Niels Gregersen et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Mitochondrial Fatty-Acid Oxidation Disorders

(2008) Michelle Kompare et al.   Seminars in Pediatric Neurology