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Journal Abstract Search

116 related items for PubMed ID: 2633993

  • 1. Hydroxyprolinemia.
    Swarna M, Rao DN, Kumari CK, Reddy PP.
    Indian J Pediatr; 1989; 56(4):527-8. PubMed ID: 2633993
    [No Abstract] [Full Text] [Related]

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  • 4. Hydroxyproline metabolism in two sisters with hydroxyprolinemia.
    Roesel RA, Blankenship PR, Lynch WR, Coryell ME, Thevaos TG, Hall WK.
    Hum Hered; 1979; 29(6):364-70. PubMed ID: 511192
    [Abstract] [Full Text] [Related]

  • 5. 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; 39(5):625-632. PubMed ID: 27139199
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  • 7. Hydroxyprolinemia: a case report.
    Rama Rao BS, Subhash MN, Narayanan HS.
    Indian Pediatr; 1974 Dec; 11(12):829-30. PubMed ID: 4448548
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  • 9. Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry.
    Baykal T, Karaaslan I, Gokcay G, Demir F, Laleli Y, Demirkol M.
    J Inherit Metab Dis; 2004 Dec; 27(6):781-2. PubMed ID: 15617190
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  • 10. [Familial hyperprolinemia].
    Dogan K, Dogan S, Lipovac K.
    Neuropsihijatrija; 1968 Dec; 16(1):15-23. PubMed ID: 5191809
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  • 12. [Hydroxyprolinemia].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Dec; (18 Pt 1):158-9. PubMed ID: 9590015
    [No Abstract] [Full Text] [Related]

  • 13. [Familial encephalopathy, imino-glycinuria, hydroxyprolinemia].
    Ghisolfi J, Augier D, Fabre J, Delsol G, Régnier C.
    Arch Fr Pediatr; 1972 Apr; 29(4):336-7. PubMed ID: 5053204
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  • 15. [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]

  • 16. Isovaleric acidemia.
    Efron ML.
    Am J Dis Child; 1967 Jan 28; 113(1):74-6. PubMed ID: 6015910
    [No Abstract] [Full Text] [Related]

  • 17. Nonketotic hyperglycinaemia. Clinical findings and amino acid analyses on the plasma of a new case.
    Ferdinand W, Gordon RR, Owen G.
    Clin Chim Acta; 1970 Dec 28; 30(3):745-9. PubMed ID: 5493897
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  • 18. Variations in clinical and laboratory findings in histidinemia.
    Waisman HA.
    Am J Dis Child; 1967 Jan 28; 113(1):93-4. PubMed ID: 6015914
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  • 19. Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
    Oyanagi K, Miura R, Yamanouchi T.
    J Pediatr; 1970 Aug 28; 77(2):259-66. PubMed ID: 5431208
    [No Abstract] [Full Text] [Related]

  • 20. Hereditary disorders of amino acid metabolism associated with mental deficiency.
    Berry HK.
    Ann N Y Acad Sci; 1969 Sep 30; 166(1):66-73. PubMed ID: 5262032
    [No Abstract] [Full Text] [Related]

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