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Journal Abstract Search

207 related items for PubMed ID: 9590105

  • 1. [Molybdenum cofactor deficiency].
    Ichida K, Hosoya T.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):474-7. PubMed ID: 9590105
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  • 2. [Classical xanthinuria (type I and II)].
    Ichida K, Hosoya T.
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):470-3. PubMed ID: 9590104
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  • 5. [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
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  • 6. 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 Nov; 405(3):379-86. PubMed ID: 3919502
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  • 12. Ophthalmic abnormalities in molybdenum cofactor deficiency and isolated sulfite oxidase deficiency.
    Lueder GT, Steiner RD.
    J Pediatr Ophthalmol Strabismus; 1995 Nov; 32(5):334-7. PubMed ID: 8531042
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  • 14. [Molybdenum cofactor deficiency].
    Matsuishi T, Ishibashi S, Nakashima M, Satoi M.
    Ryoikibetsu Shokogun Shirizu; 1998 Nov; (19 Pt 2):185-8. PubMed ID: 9645039
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  • 19. Blood uric acid as a pointer to the diagnosis of molybdenum cofactor deficiency.
    Coşkun T, Yetük M, Yurdakök M, Tekinalp G.
    Acta Paediatr; 1998 Jun; 87(6):714-5. PubMed ID: 9686674
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