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Journal Abstract Search

115 related items for PubMed ID: 1779639

  • 1. Attempt at treatment with tetrahydrobiopterin in combined deficiency of xanthine oxidase and sulphite oxidase.
    Fujitaka M, Sakura N, Ueda K, Konishi H, Yoshida S, Yamasaki T.
    J Inherit Metab Dis; 1991; 14(5):843-4. PubMed ID: 1779639
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  • 3. Antenatal diagnosis of combined xanthine and sulphite oxidase deficiencies.
    Ogier H, Wadman SK, Johnson JL, Saudubray JM, Duran M, Boue J, Munnich A, Charpentier C.
    Lancet; 1983 Dec 10; 2(8363):1363-4. PubMed ID: 6139694
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  • 4. Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor.
    Roesel RA, Bowyer F, Blankenship PR, Hommes FA.
    J Inherit Metab Dis; 1986 Dec 10; 9(4):343-7. PubMed ID: 3104671
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  • 5. Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor.
    Bonioli E, DiStefano A, Palmieri A, Bertola A, Bellini C, Caruso U, Fantasia AR, Minniti G, Dorche C.
    J Inherit Metab Dis; 1996 Dec 10; 19(5):700-1. PubMed ID: 8892030
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  • 6. Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?
    Duran M, Beemer FA, van de Heiden C, Korteland J, de Bree PK, Brink M, Wadman SK, Lombeck I.
    J Inherit Metab Dis; 1978 Dec 10; 1(4):175-8. PubMed ID: 117254
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  • 8. Anatomo-pathological findings in a case of combined deficiency of sulphite oxidase and xanthine oxidase with a defect of molybdenum cofactor.
    Roth A, Nogues C, Monnet JP, Ogier H, Saudubray JM.
    Virchows Arch A Pathol Anat Histopathol; 1985 Dec 10; 405(3):379-86. PubMed ID: 3919502
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  • 12. A new case of isolated sulphite oxidase deficiency with rapid fatal outcome.
    Vianey-Liaud C, Desjacques P, Gaulme J, Dorche C, Vanlieferinghen P, Dechelotte P, Divry P.
    J Inherit Metab Dis; 1988 Dec 10; 11(4):425-6. PubMed ID: 3149702
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  • 14. Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?
    van der Heiden C, Beemer FA, Brink W, Wadman SK, Duran M.
    Clin Biochem; 1979 Dec 10; 12(6):206-8. PubMed ID: 583402
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  • 18. A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, beta-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency.
    Crawhall JC.
    Clin Biochem; 1985 Jun 10; 18(3):139-42. PubMed ID: 3888441
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  • 20. [Molybdenum cofactor deficiency].
    Ichida K, Hosoya T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jun 10; (18 Pt 1):474-7. PubMed ID: 9590105
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