Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: Improved survival by prompt diagnosis

Identification of methylenecyclopropyl acetic acid in serum of European horses with atypical myopathy

(2013) D.-M. Votion et al.   EQUINE VETERINARY JOURNAL

Seasonal pasture myopathy/atypical myopathy in North America associated with ingestion of hypoglycin A within seeds of the box elder tree

(2012) S. J. Valberg et al.   EQUINE VETERINARY JOURNAL

Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening

(2010) Ute Spiekerkoetter   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

Propofol Infusion Syndrome

(2008) Vincenzo Fodale et al.   DRUG SAFETY

Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy

(2008) C.M. Westermann et al.   NEUROMUSCULAR DISORDERS