| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
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| Cheng ML et al. | Metabolic disturbances identified in plasma are associated with outcomes in patients with heart failure: diagnostic and prognostic value of metabolomics. | 2015 | J. Am. Coll. Cardiol. | pmid:25881932 |
| Alexandre-Gouabau MC et al. | Maternal and cord blood LC-HRMS metabolomics reveal alterations in energy and polyamine metabolism, and oxidative stress in very-low birth weight infants. | 2013 | J. Proteome Res. | pmid:23527880 |
| Gallant NM et al. | Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California. | 2012 | Mol. Genet. Metab. | pmid:22424739 |
| van Maldegem BT et al. | Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency. | 2010 | Pediatr. Res. | pmid:19952864 |
| Forni S et al. | Rapid determination of C4-acylcarnitine and C5-acylcarnitine isomers in plasma and dried blood spots by UPLC-MS/MS as a second tier test following flow-injection MS/MS acylcarnitine profile analysis. | 2010 | Mol. Genet. Metab. | pmid:20591710 |
| Beattie SG et al. | Biochemical correction of short-chain acyl-coenzyme A dehydrogenase deficiency after portal vein injection of rAAV8-SCAD. | 2008 | Hum. Gene Ther. | pmid:18500942 |
| Srinivas SR et al. | Transport of butyryl-L-carnitine, a potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB(0,+). | 2007 | Am. J. Physiol. Gastrointest. Liver Physiol. | pmid:17855766 |
| Merinero B et al. | Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathy. | 2006 | J. Inherit. Metab. Dis. | pmid:16906473 |
| van Maldegem BT et al. | Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency. | 2006 | JAMA | pmid:16926354 |
| Conlon TJ et al. | Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vector. | 2006 | Hum. Gene Ther. | pmid:16409126 |
| Hack A et al. | Monitoring of ketogenic diet for carnitine metabolites by subcutaneous microdialysis. | 2006 | Pediatr. Res. | pmid:16690958 |
| Kuster T et al. | Filter paper cards contaminated with EMLA cream produce artefacts on acylcarnitine analysis. | 2004 | J. Inherit. Metab. Dis. | pmid:15669691 |
| Nagan N et al. | The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C(4)-acylcarnitine concentration in newborn blood spots. | 2003 | Mol. Genet. Metab. | pmid:12706374 |
| Koeberl DD et al. | Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. | 2003 | Pediatr. Res. | pmid:12736383 |
| Lozano P et al. | Ester synthesis from trimethylammonium alcohols in dry organic media catalyzed by immobilized Candida antarctica lipase B. | 2003 | Biotechnol. Bioeng. | pmid:12599262 |
| Young SP et al. | A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency. | 2003 | Clin. Chim. Acta | pmid:14568186 |
| Tyni T et al. | Analysis of mitochondrial fatty acid oxidation intermediates by tandem mass spectrometry from intact mitochondria prepared from homogenates of cultured fibroblasts, skeletal muscle cells, and fresh muscle. | 2002 | Pediatr. Res. | pmid:12084849 |
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Butyrylcarnitine
Butyrylcarnitine is a lipid of Fatty Acyls (FA) class.
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