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Journal Abstract Search

179 related items for PubMed ID: 4393577

  • 1. 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]

  • 2. [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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  • 4. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 28; 17(3):297-315. PubMed ID: 5387412
    [No Abstract] [Full Text] [Related]

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  • 6. [Familial hyperprolinemia].
    Dogan K, Dogan S, Lipovac K.
    Neuropsihijatrija; 1968 Oct 28; 16(1):15-23. PubMed ID: 5191809
    [No Abstract] [Full Text] [Related]

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  • 9. Hyperprolinemia: clinical and biochemical family study.
    Woody NC, Snyder CH, Harris JA.
    Pediatrics; 1969 Oct 28; 44(4):554-63. PubMed ID: 5346634
    [No Abstract] [Full Text] [Related]

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  • 11. Hydroxyprolinemia as an illustration of nonessential enzymes in man.
    Prockop DJ.
    N Engl J Med; 1970 Aug 27; 283(9):487. PubMed ID: 5434118
    [No Abstract] [Full Text] [Related]

  • 12. A heritable disorder of connective tissue. Hydroxylysine-deficient collagen disease.
    Pinnell SR, Krane SM, Kenzora JE, Glimcher MJ.
    N Engl J Med; 1972 May 11; 286(19):1013-20. PubMed ID: 5016372
    [No Abstract] [Full Text] [Related]

  • 13. Genetic cause and prevalence of hydroxyprolinemia.
    Staufner C, Haack TB, Feyh P, Gramer G, Raga DE, Terrile C, Sauer S, Okun JG, Fang-Hoffmann J, Mayatepek E, Prokisch H, Hoffmann GF, Kölker S.
    J Inherit Metab Dis; 2016 Sep 11; 39(5):625-632. PubMed ID: 27139199
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  • 15. Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.
    Jackson SH, Dennis AW, Greenberg M.
    Can Med Assoc J; 1975 Oct 18; 113(8):759, 762-3. PubMed ID: 803128
    [Abstract] [Full Text] [Related]

  • 16. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G, Farriaux JP, Dautrevaux M.
    Helv Paediatr Acta; 1970 Apr 18; 25(2):165-75. PubMed ID: 5419477
    [No Abstract] [Full Text] [Related]

  • 17. [Hypersarcosinemia with sarcosinuria. Study of a new case].
    Willems C, Heusden A, Hainaut A, Chapelle P.
    J Genet Hum; 1971 Mar 18; 19(1):101-18. PubMed ID: 5158355
    [No Abstract] [Full Text] [Related]

  • 18. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J, Guardiola Vicente JM, Botella García J.
    Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371
    [No Abstract] [Full Text] [Related]

  • 19. Iminoglycinuria--a "harmless" inborn error of metabolism?
    Fraser GR, Friedmann AI, Patton VM, Wade DN, Woolf LI.
    Humangenetik; 1968 Jul 31; 6(4):362-7. PubMed ID: 5713621
    [No Abstract] [Full Text] [Related]

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