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Journal Abstract Search

122 related items for PubMed ID: 5191809

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

  • 2. 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]

  • 3. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F, Pavone L, Antener I.
    Pediatrics; 1971 Aug 27; 48(2):225-31. PubMed ID: 5560617
    [No Abstract] [Full Text] [Related]

  • 4. [Familial essential hyperprolinemia].
    Hainaut H, Hariga J, Willems C, Heusden A, Chapelle P.
    Presse Med (1893); 1971 Apr 24; 79(21):945-8. PubMed ID: 5580522
    [No Abstract] [Full Text] [Related]

  • 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]

  • 6. [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]

  • 7. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 31; 17(3):297-315. PubMed ID: 5387412
    [No Abstract] [Full Text] [Related]

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  • 9. [Familial hyperprolinemia--a case in a family].
    Oknińska A, Grygalewicz J, Kowalewska-Kantecka B, Iwańska J.
    Pol Arch Med Wewn; 1974 Feb 31; 51(2):189-97. PubMed ID: 4816363
    [No Abstract] [Full Text] [Related]

  • 10. [Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
    Jeune M, Collombel C, Michel M, David M, Guibaud P, Guerrier G, Albert J.
    Ann Pediatr (Paris); 1970 Feb 02; 17(2):349-63. PubMed ID: 5513158
    [No Abstract] [Full Text] [Related]

  • 11. Defective hydroxyproline metabolism in type II hyperprolinemia.
    Goodman SI, Mace JW, Miles BS, Teng CC, Brown SB.
    Biochem Med; 1974 Aug 02; 10(4):329-36. PubMed ID: 4851275
    [No Abstract] [Full Text] [Related]

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  • 14. Hyperprolinemia. I. Study of a large family.
    Potter JL, Waickman FJ.
    J Pediatr; 1973 Oct 02; 83(4):635-8. PubMed ID: 4729989
    [No Abstract] [Full Text] [Related]

  • 15. Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes.
    Valle D, Goodman SI, Applegarth DA, Shih VE, Phang JM.
    J Clin Invest; 1976 Sep 02; 58(3):598-603. PubMed ID: 956388
    [Abstract] [Full Text] [Related]

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  • 17. [Hyperprolinemia type I].
    Thomsen B, Vetner M, Rosleff F, Reske-Nielsen E.
    Ugeskr Laeger; 1974 Oct 28; 136(44):2460-1. PubMed ID: 4420280
    [No Abstract] [Full Text] [Related]

  • 18. Familial hyperprolinemia without mental retardation and hereditary nephropathy.
    Mollica F, Pavone L, Antener I.
    Monogr Hum Genet; 1972 Oct 28; 6():144-5. PubMed ID: 4663888
    [No Abstract] [Full Text] [Related]

  • 19. [Hyperprolinemia type I].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Oct 28; (18 Pt 1):152-4. PubMed ID: 9590013
    [No Abstract] [Full Text] [Related]

  • 20. [Inborn errors of imino acid metabolism].
    Endo F.
    Nihon Rinsho; 1992 Jul 28; 50(7):1568-74. PubMed ID: 1404885
    [Abstract] [Full Text] [Related]

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