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Cerebral infarction and pancreatitis: possible complications of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Huemer M, Muehl A, Wandl-Vergesslich K, Strobl W, Wanders RJ, Stoeckler-Ipsiroglu S (1998) Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase de¢ciency. Eur J Pediatr 157: 743–746.

    PubMed  Google Scholar 

  • Ozand PT, Al Aqeel A, Gascon G, Brismar J, Thomas E, Gleispach H (1991) 3-Hydroxy-3-methyglutaryl-coenzyme A (HMG-CoA) lyase de¢ciency in Saudi Arabia. J Inherit Metab Dis 14: 174–188.

    PubMed  Google Scholar 

  • Wilson WG, Cass MB, Sovik O, Gibson KM, Sweetman L (1984) A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase de¢ciency. Eur J Pediatr 142: 289–291.

    PubMed  Google Scholar 

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Authors and Affiliations

  1. Department of Pediatrics, Kyoto University Hospital, 54 Shogoin Sakyo, Kyoto, 606-8507, Japan

    J. Muroi, T. Yorifuji, A. Uematsu & T. Nakahata

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  1. J. Muroi
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  2. T. Yorifuji
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  3. A. Uematsu
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  4. T. Nakahata
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Muroi, J., Yorifuji, T., Uematsu, A. et al. Cerebral infarction and pancreatitis: possible complications of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. J Inherit Metab Dis 23, 636–637 (2000). https://doi.org/10.1023/A:1005642316174

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  • DOI: https://doi.org/10.1023/A:1005642316174

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