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PUBMED FOR HANDHELDS

Journal Abstract Search


276 related items for PubMed ID: 8976110

  • 1. [Inherited disorders of uric acid metabolism--classification, enzymatic- and DNA-diagnosis].
    Iwahana H, Itakura M.
    Nihon Rinsho; 1996 Dec; 54(12):3303-8. PubMed ID: 8976110
    [Abstract] [Full Text] [Related]

  • 2. Disorders associated with purine and pyrimidine metabolism.
    Edwards NL, Fox IH.
    Spec Top Endocrinol Metab; 1984 Dec; 6():95-140. PubMed ID: 6098039
    [Abstract] [Full Text] [Related]

  • 3. [PRPP synthetase superactivity].
    Fujimori S.
    Nihon Rinsho; 1996 Dec; 54(12):3309-14. PubMed ID: 8976111
    [Abstract] [Full Text] [Related]

  • 4. Inherited disorders of purine metabolism--underlying molecular mechanisms.
    Gutensohn W.
    Klin Wochenschr; 1984 Oct 15; 62(20):953-62. PubMed ID: 6209448
    [Abstract] [Full Text] [Related]

  • 5. [Hypouricemia--definition and classification].
    Fujimori S.
    Nihon Rinsho; 2003 Jan 15; 61 Suppl 1():353-6. PubMed ID: 12629745
    [No Abstract] [Full Text] [Related]

  • 6. [Hereditary anomalies of purine metabolism. Current biochemical aspects].
    Perignon JL, Cartier P.
    Arch Fr Pediatr; 1980 Oct 15; 37(8):487-90. PubMed ID: 6255885
    [No Abstract] [Full Text] [Related]

  • 7. Patterns of phosphoribosylpyrophosphate and ribose-5-phosphate concentration and generation in fibroblasts from patients with gout and purine overproduction.
    Becker MA.
    J Clin Invest; 1976 Feb 15; 57(2):308-18. PubMed ID: 176178
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  • 10. [Hyperuricemia associated with inborn errors of purine metabolism: screening, enzymatic and genetic diagnosis].
    Yamada Y.
    Nihon Rinsho; 2003 Jan 15; 61 Suppl 1():278-83. PubMed ID: 12629731
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  • 15. [PRPP synthetase deficiency].
    Kawasugi K, Takeuchi F.
    Nihon Rinsho; 2003 Jan 15; 61 Suppl 1():383-5. PubMed ID: 12629752
    [No Abstract] [Full Text] [Related]

  • 16. Kinetic aspects of purine metabolism in cultured fibroblasts. A comparative study of cells from patients overproducing purines due to HGPRT deficiency and PRPP synthetase superactivity.
    Zoref E, de Vries A, Sperling O.
    Monogr Hum Genet; 1978 Jan 15; 10():96-9. PubMed ID: 214700
    [No Abstract] [Full Text] [Related]

  • 17. Molecular analysis of two enzyme genes, HPRT1 and PRPS1, causing X-linked inborn errors of purine metabolism.
    Yamada Y, Yamada K, Nomura N, Yamano A, Kimura R, Tomida S, Naiki M, Wakamatsu N.
    Nucleosides Nucleotides Nucleic Acids; 2010 Jun 15; 29(4-6):291-4. PubMed ID: 20544509
    [Abstract] [Full Text] [Related]

  • 18. [Typing of hypouricemia (uric acid clearance)].
    Tsutani H, Takagi K.
    Nihon Rinsho; 2003 Jan 15; 61 Suppl 1():357-60. PubMed ID: 12629746
    [No Abstract] [Full Text] [Related]

  • 19. Genetic defects in human purine and pyrimidine metabolism.
    Boss GR, Seegmiller JE.
    Annu Rev Genet; 1982 Jan 15; 16():297-328. PubMed ID: 6297375
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  • 20. [Animal models for abnormal purine metabolism].
    Morisaki T.
    Nihon Rinsho; 2003 Jan 15; 61 Suppl 1():482-6. PubMed ID: 12629770
    [No Abstract] [Full Text] [Related]


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