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Identification of glutarylcarnitine in glutaric aciduria type 1

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Journal of Inherited Metabolic Disease

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References

  • Bohmer, T. and Bremer, J. Propionylcarnitine, physiological variationsin vivo.Biochim. Biophys. Acta 152 (1968) 559–567

    PubMed  Google Scholar 

  • Chalmers, R. A., Roe, C. R., Stacey, T. E. and Hoppel, C. L. Urinary excretion ofl-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency ofl-carnitine.Pediatr. Res. 18 (1984) 1325–1328

    PubMed  Google Scholar 

  • Goodman, S. I., Markey, S. P., Moe, P. G., Miles B. S. and Teng, C. C. Glutaric aciduria: a ‘new’ disorder of amino acid metabolism.Biochem. Med. 12 (1975) 12–21

    PubMed  Google Scholar 

  • Kerner, J. and Bieber, L. L. A radioisotopic-exchange method for quantitation of short-chain (acid-soluble) acylcarnitines.Anal. Biochem. 134 (1983) 459–466

    PubMed  Google Scholar 

  • Kidouchi, K. Studies on measurement of organic acids by carboxylic acid analyzer: 1. basic study; 2. clinical study.J. Nagoya City Med. Ass. 36 (1985) 285–307

    Google Scholar 

  • Millington, D. S., Bohan, T. P., Roe, C. R., Yergey, A. L. and Liberato, D. J. Valproylcarnitine: a novel drug metabolite identified by fast atom bombardment and thermospray liquid chromatography-mass spectrometry.Clin. Chim. Acta 145 (1985) 69–76

    PubMed  Google Scholar 

  • Seccombe, D. W., James, L. and Booth, F.l-Carnitine treatment in glutaric aciduria type 1.Neurology 36 (1986) 264–267

    PubMed  Google Scholar 

  • Sugiyama, N., Morishita, H., Kobayashi, M., Wada, Y., Shimoda, H., Suzawa, T. and Yoshimitsu, K. Dose-dependent effect of carnitine on propionate elimination in propionic acidemia and methylmalonic aciduria.Brain Dev. (Tokyo) 8 (1986) 204

    Google Scholar 

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Authors and Affiliations

  1. Department of Pediatrics, Nagoya City Higashi General Hospital, 1-2-23 Wakamizu, Chikusa-ku, 464, Nagoya, Japan

    K. Kidouchi

  2. Department of Pediatrics, Nagoya City University Medical School, 1 Kawasumi, Mizuho-ku, 467, Nagoya, Japan

    N. Sugiyama, H. Morishita, M. Kobayashi & Y. Wada

  3. Faculty of Pharmaceutical Sciences, Nagoya City University, 3-1, Tanabe-dori, Mizuho-ku, 467, Nagoya, Japan

    S. Nagai & J. Sakakibara

Authors
  1. K. Kidouchi
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  2. N. Sugiyama
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  3. H. Morishita
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  4. M. Kobayashi
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  5. Y. Wada
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  6. S. Nagai
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  7. J. Sakakibara
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Kidouchi, K., Sugiyama, N., Morishita, H. et al. Identification of glutarylcarnitine in glutaric aciduria type 1. J Inherit Metab Dis 10 (Suppl 2), 279–281 (1987). https://doi.org/10.1007/BF01811426

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  • DOI: https://doi.org/10.1007/BF01811426

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