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Journal Abstract Search

204 related items for PubMed ID: 9645039

  • 1. [Molybdenum cofactor deficiency].
    Matsuishi T, Ishibashi S, Nakashima M, Satoi M.
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):185-8. PubMed ID: 9645039
    [No Abstract] [Full Text] [Related]

  • 2. [Isolated sulfite oxidase deficiency].
    Matsuishi T, Wada N, Isakai T, Togo A.
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):189-91. PubMed ID: 9645040
    [No Abstract] [Full Text] [Related]

  • 3. [Combined sulfite and xanthine oxidase deficiency due to an anomaly in the metabolism of molybdenum cofactor].
    Lagier P, Tessonnier JM, Collet S, Lando A, Divry P, Vianet-Liaud C, Desjacques P, Bimar J.
    Ann Pediatr (Paris); 1986 Nov; 33(9):825-8. PubMed ID: 3800248
    [No Abstract] [Full Text] [Related]

  • 4. Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.
    Johnson JL, Waud WR, Rajagopalan KV, Duran M, Beemer FA, Wadman SK.
    Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3715-9. PubMed ID: 6997882
    [Abstract] [Full Text] [Related]

  • 5. [Sulfite and xanthine oxidase deficiency: a diagnosis based on 2 simple tests].
    Hervé F, Berger JP, Soulier J.
    Ann Pediatr (Paris); 1986 Nov; 33(9):857. PubMed ID: 3800254
    [No Abstract] [Full Text] [Related]

  • 6. 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 Nov; 19(5):700-1. PubMed ID: 8892030
    [No Abstract] [Full Text] [Related]

  • 7. Diagnosis of molybdenum cofactor deficiency.
    Simmonds HA, Hoffmann GF, Pérignon JL, Micheli V, van Gennip AH.
    Lancet; 1999 Feb 20; 353(9153):675. PubMed ID: 10030363
    [No Abstract] [Full Text] [Related]

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  • 9. 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 Feb 20; 9(4):343-7. PubMed ID: 3104671
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  • 11. [Molybdenum cofactor deficiency].
    Ichida K, Hosoya T.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb 20; (18 Pt 1):474-7. PubMed ID: 9590105
    [No Abstract] [Full Text] [Related]

  • 12. Urinary AASA excretion is elevated in patients with molybdenum cofactor deficiency and isolated sulphite oxidase deficiency.
    Mills PB, Footitt EJ, Ceyhan S, Waters PJ, Jakobs C, Clayton PT, Struys EA.
    J Inherit Metab Dis; 2012 Nov 20; 35(6):1031-6. PubMed ID: 22403017
    [Abstract] [Full Text] [Related]

  • 13. Molybdenum cofactor deficiency in two siblings: diagnostic difficulties.
    Hansen LK, Wulff K, Dorche C, Christensen E.
    Eur J Pediatr; 1993 Aug 20; 152(8):662-4. PubMed ID: 8404970
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  • 16. 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 Aug 20; 405(3):379-86. PubMed ID: 3919502
    [Abstract] [Full Text] [Related]

  • 17. Molybdenum cofactor deficiency in a patient previously characterized as deficient in sulfite oxidase.
    Johnson JL, Wuebbens MM, Mandell R, Shih VE.
    Biochem Med Metab Biol; 1988 Aug 20; 40(1):86-93. PubMed ID: 3219233
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  • 18. Biochemical investigation of a child with molybdenum cofactor deficiency.
    Bamforth FJ, Johnson JL, Davidson AG, Wong LT, Lockitch G, Applegarth DA.
    Clin Biochem; 1990 Dec 20; 23(6):537-42. PubMed ID: 2289312
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  • 20. An HPLC assay for detection of elevated urinary S-sulphocysteine, a metabolic marker of sulphite oxidase deficiency.
    Johnson JL, Rajagopalan KV.
    J Inherit Metab Dis; 1995 Dec 20; 18(1):40-7. PubMed ID: 7623441
    [Abstract] [Full Text] [Related]

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