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Journal Abstract Search

179 related items for PubMed ID: 4393577

  • 21. Hydroxyprolinemia. 3. The origin of free hydroxyproline in hydroxyprolinemia. Collagen turnover. Evidence for biosynthetic pathway in man.
    Efron ML, Bixby EM, Hockaday TD, Smith LH, Meshorer E.
    Biochim Biophys Acta; 1968 Sep 03; 165(2):238-50. PubMed ID: 5683524
    [No Abstract] [Full Text] [Related]

  • 22. Hydroxyproline metabolism in type II hyperprolinaemia.
    Similä S.
    Ann Clin Biochem; 1979 Jul 03; 16(4):177-81. PubMed ID: 533224
    [Abstract] [Full Text] [Related]

  • 23. Biochemical, morphological and hybrid studies in hyperprolinemic mice.
    Kanwar YS, Krakower CA, Manaligod JR, Justice P, Wong PW.
    Biomedicine; 1975 May 03; 22(3):209-16. PubMed ID: 240452
    [Abstract] [Full Text] [Related]

  • 24. [Familial iminoglycinuria].
    Ohura T.
    Ryoikibetsu Shokogun Shirizu; 1998 May 03; (19 Pt 2):569-71. PubMed ID: 9645136
    [No Abstract] [Full Text] [Related]

  • 25. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):430-1. PubMed ID: 4681731
    [No Abstract] [Full Text] [Related]

  • 26. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".
    Statter M, Ben-Zvi A, Shina A, Schein R, Russell A.
    Helv Paediatr Acta; 1976 Aug 13; 31(2):173-82. PubMed ID: 955941
    [Abstract] [Full Text] [Related]

  • 27. Glycylproline peptiduria in familial hyperostosis of obscure nature.
    Alderman MH, Frimpter GW, Isaacs M, Scheiner E.
    Metabolism; 1969 Aug 13; 18(8):692-9. PubMed ID: 4895065
    [No Abstract] [Full Text] [Related]

  • 28. Ocular manifestations of familial hyperlysinemia.
    Smith TH, Holland MG, Woody NC.
    Trans Am Acad Ophthalmol Otolaryngol; 1971 Aug 13; 75(2):355-60. PubMed ID: 5557172
    [No Abstract] [Full Text] [Related]

  • 29. [Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
    Minder FC, Dubach UC, Antener I.
    Z Klin Med; 1965 Dec 31; 158(7):601-32. PubMed ID: 5869106
    [No Abstract] [Full Text] [Related]

  • 30. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L, Navarro J, Aymard P, Baudon JJ, Mondet Y, Polonovski C, Laplane R.
    Arch Fr Pediatr; 1972 Dec 31; 29(7):713-36. PubMed ID: 4644461
    [No Abstract] [Full Text] [Related]

  • 31. Hydroxyprolinemia.
    Swarna M, Rao DN, Kumari CK, Reddy PP.
    Indian J Pediatr; 1989 Dec 31; 56(4):527-8. PubMed ID: 2633993
    [No Abstract] [Full Text] [Related]

  • 32. Hydroxyprolinemia: a case report.
    Rama Rao BS, Subhash MN, Narayanan HS.
    Indian Pediatr; 1974 Dec 31; 11(12):829-30. PubMed ID: 4448548
    [No Abstract] [Full Text] [Related]

  • 33. [Hydroxyprolinemia].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Dec 31; (18 Pt 1):158-9. PubMed ID: 9590015
    [No Abstract] [Full Text] [Related]

  • 34. Hydroxyproline metabolism in two sisters with hydroxyprolinemia.
    Roesel RA, Blankenship PR, Lynch WR, Coryell ME, Thevaos TG, Hall WK.
    Hum Hered; 1979 Dec 31; 29(6):364-70. PubMed ID: 511192
    [Abstract] [Full Text] [Related]

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