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PUBMED FOR HANDHELDS

Journal Abstract Search


182 related items for PubMed ID: 533224

  • 1. Hydroxyproline metabolism in type II hyperprolinaemia.
    Similä S.
    Ann Clin Biochem; 1979 Jul; 16(4):177-81. PubMed ID: 533224
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  • 2. Defective hydroxyproline metabolism in type II hyperprolinemia.
    Goodman SI, Mace JW, Miles BS, Teng CC, Brown SB.
    Biochem Med; 1974 Aug; 10(4):329-36. PubMed ID: 4851275
    [No Abstract] [Full Text] [Related]

  • 3. N-(pyrrole-2-carboxyl) glycine a diagnostic marker of hyperprolinaemia type II: mass spectra of trimethylsilyl derivatives.
    Walker V, Mills GA.
    Clin Chim Acta; 2009 Jul; 405(1-2):153-4. PubMed ID: 19376100
    [No Abstract] [Full Text] [Related]

  • 4. Type II hyperprolinemia: a case report.
    Onenli-Mungan N, Yüksel B, Elkay M, Topaloğlu AK, Baykal T, Ozer G.
    Turk J Pediatr; 2004 Jul; 46(2):167-9. PubMed ID: 15214748
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  • 5. [Hyperprolinemia and hydroxyprolinemia].
    Berger R, Broyer M.
    Presse Med (1893); 1969 May 28; 77(26):957-8. PubMed ID: 5795142
    [No Abstract] [Full Text] [Related]

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  • 8. Genetic evidence for a common enzyme catalyzing the second step in the degradation of proline and hydroxyproline.
    Valle D, Goodman SI, Harris SC, Phang JM.
    J Clin Invest; 1979 Nov 28; 64(5):1365-70. PubMed ID: 500817
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  • 12. Low proline diet in type I hyperprolinaemia.
    Harries JT, Piesowicz AT, Seakins JW, Francis DE, Wolff OH.
    Arch Dis Child; 1971 Feb 28; 46(245):72-81. PubMed ID: 5555491
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  • 13. Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs.
    Pavone L, Mollica F, Levy HL.
    Arch Dis Child; 1975 Aug 28; 50(8):637-41. PubMed ID: 1200680
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  • 14. Iminoglycinuria in a child in Czechoslovakia.
    Blehová B, Păzoutová N, Hyánek J, Jirásek J.
    Humangenetik; 1973 Jul 20; 19(2):207-10. PubMed ID: 4744406
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  • 17. Iminoglycinuria: a benign type of inherited aminoaciduria.
    Coşkun T, Ozalp I, Tokatli A.
    Turk J Pediatr; 1993 Jul 20; 35(2):121-5. PubMed ID: 7504361
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  • 19. Hyperprolinaemia type 2.
    Emery FA, Goldie L, Stern J.
    J Ment Defic Res; 1968 Sep 20; 12(3):187-95. PubMed ID: 4972625
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  • 20. Hydroxyprolinemia: an apparently harmless familial metabolic disorder.
    Pelkonen R, Kivirikko KI.
    N Engl J Med; 1970 Aug 27; 283(9):451-6. PubMed ID: 4393577
    [No Abstract] [Full Text] [Related]


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