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Multiple acyl-CoA dehydrogenase deficiency: A neonatal onset case responsive to treatment

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Journal of Inherited Metabolic Disease

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References

  • Danks, D. M., Brown, G. K., Haan, E. A., Hunt, S. and Schloem, R. Malonyl-CoA decarboxylase deficiency—a further case with an unusual pattern of organic acids in the urine.22nd Annual Symposium of Society for the Study of Inborn Errors of Metabolism, Newcastle-upon-Tyne, 5–7 September 1984, Abstract. P-83.

  • Goodman, S. I. and Markey, S. P.Diagnosis of Organic Acidemias by Gas Chromatography—Mass Spectrometry, Alan R. Liss, New York, 1981, pp. 105–114

    Google Scholar 

  • Goodman, S. I., Stene, D. O., McCabe, E. R. B., Norenberg, M. D., Shikes, R. H., Stumpf, D. A. and Blackburn, G. K. Glutaric acidemia type II: Clinical, biochemical, and morphologic considerations.J. Pediatr. 100 (1982) 946–950

    PubMed  Google Scholar 

  • Goodman, S. I., Reale, M. and Berlow, S. Glutaric acidemia type II: A form with deleterious intrauterine effects.J. Pediatr. 102 (1983) 411–413

    PubMed  Google Scholar 

  • Gregerson, N., Wintzensen, H., Kolvraa, S., Christensen, E., Christensen, M. F., Brandt, N. J. and Rasmussen, K. C6-C10-Dicarboxylic aciduria: Investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.Pediatr. Res. 16 (1982) 861–868

    PubMed  Google Scholar 

  • Mamer, O. A. and Gibbs, B. F. Simplified gas chromatography of trimethylsilyl esters of C1 through C5 fatty acids in serum and urine.Clin. Chem. 19 (1973) 1006–1009

    PubMed  Google Scholar 

  • Mantagos, S., Genel, M. and Tanaka, K. Ethylmalonic-adipic aciduria:In vivo andin vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases.J. Clin. Invest. 64 (1979) 1580–1589

    PubMed  Google Scholar 

  • McGarry, J. D. and Foster, D. W. An improved and simplified radioisotopic assay for the determination of free and esterified carnitine.J. Lipid Res. 17 (1976) 277–280

    PubMed  Google Scholar 

  • Verjee, Z. H. and Sherwood, W. G. Plasma amino acids in Reye's syndrome.Clin. Chem. 30 (1984) 944, Abstract 24

    Google Scholar 

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Authors and Affiliations

  1. Department of Clinical Biochemistry and the Research Institute, Hospital for Sick Children, M5G 1X8, Toronto, Ontario, Canada

    Z. H. Verjee & W. G. Sherwood

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  1. Z. H. Verjee
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  2. W. G. Sherwood
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Verjee, Z.H., Sherwood, W.G. Multiple acyl-CoA dehydrogenase deficiency: A neonatal onset case responsive to treatment. J Inherit Metab Dis 8 (Suppl 2), 137–138 (1985). https://doi.org/10.1007/BF01811497

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