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Journal Abstract Search

150 related items for PubMed ID: 4365835

  • 41. Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract.
    Harley JD, Mutton P, Irvine S, Gupta JD.
    Lancet; 1974 Aug 03; 2(7875):259-61. PubMed ID: 4136146
    [No Abstract] [Full Text] [Related]

  • 42. [Early detection of hereditary metabolic diseases (author's transl)].
    Steuer W.
    Offentl Gesundheitswes; 1980 Dec 03; 42(12):949-54. PubMed ID: 6451829
    [No Abstract] [Full Text] [Related]

  • 43. [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 03; 29(7):713-36. PubMed ID: 4644461
    [No Abstract] [Full Text] [Related]

  • 44. [Activity of galaktose-1-phosphate-uridyltransferase in erythrozytes of galactosemia heterocygotes of different ages (author's transl)].
    Kaloud H, Sitzmann FC.
    Padiatr Padol; 1971 Dec 03; 6(3):268-73. PubMed ID: 5164142
    [No Abstract] [Full Text] [Related]

  • 45. Detection of heterozygotes for galactokinase deficiency in a human population.
    Mayes JS, Guthrie R.
    Biochem Genet; 1968 Nov 03; 2(3):219-30. PubMed ID: 5715186
    [No Abstract] [Full Text] [Related]

  • 46. A simple assay for galactokinase using DEAE-cellulose column chromatography.
    Shin-Buehring YS, Osang M, Ziegler R, Schaub J.
    Clin Chim Acta; 1977 Jan 03; 74(1):1-5. PubMed ID: 12888
    [No Abstract] [Full Text] [Related]

  • 47. Studies of amniotic fluid and cord blood in an infant with alpha 1-antitrypsin deficiency.
    Kaiser D, Rennert OM, Goedde HW, Benkmann HG, Wuilloud H, Kehrli P, Sollberger H.
    Humangenetik; 1974 Jan 03; 25(3):241-5. PubMed ID: 4548687
    [No Abstract] [Full Text] [Related]

  • 48. [Clinical and biochemical findings in a child with hereditary galactokinase defect].
    Kaloud H, Sitzmann FC, Mayer R, Paltauf F.
    Klin Padiatr; 1973 Jan 03; 185(1):18-22. PubMed ID: 4734834
    [No Abstract] [Full Text] [Related]

  • 49. [Pyruvate kinase deficiciency (author's transl)].
    Miwa S.
    Rinsho Ketsueki; 1973 Dec 03; 14(0):1325-30. PubMed ID: 4807678
    [No Abstract] [Full Text] [Related]

  • 50. On the screening for inborn errors of galactose metabolism.
    Vaca G, Sànchez-Corona J, Olivares N, Medina C, Ibarra B, Cantú JM.
    Ann Genet; 1983 Dec 03; 26(3):191-2. PubMed ID: 6606384
    [Abstract] [Full Text] [Related]

  • 51. [Biochemical and clinical findings in congenital abnormalities of galactose metabolism (author's transl)].
    Sitzmann FC, Kaloud H, Istvan L.
    Wien Klin Wochenschr; 1975 Jan 10; 87(1):12-8. PubMed ID: 1130073
    [Abstract] [Full Text] [Related]

  • 52. Alpha-1-antitrypsin deficiency and disease.
    Alper CA, Johnson AM.
    Pediatrics; 1970 Dec 10; 46(6):837-40. PubMed ID: 4923511
    [No Abstract] [Full Text] [Related]

  • 53. Cataracts and galactokinase deficiency.
    Beutler E.
    N Engl J Med; 1972 Jul 27; 287(4):202-3. PubMed ID: 5033541
    [No Abstract] [Full Text] [Related]

  • 54. [Studies on a family with galactosemia].
    von Berg W.
    Dtsch Med Wochenschr; 1969 Jan 27; 94(2):61-5. PubMed ID: 5782691
    [No Abstract] [Full Text] [Related]

  • 55. Hereditary deficiency of adenylate kinase in red blood cell.
    Szeinberg A, Kahana D, Gavendo S, Zaidman J, Ben-Ezzer J.
    Acta Haematol; 1969 Jan 27; 42(2):111-26. PubMed ID: 4982580
    [No Abstract] [Full Text] [Related]

  • 56. Screening for susceptibility to drug reactions. Cholinesterase mutants.
    Szeinberg A.
    Isr J Med Sci; 1973 Jan 27; 9(9):1355-7. PubMed ID: 4775117
    [No Abstract] [Full Text] [Related]

  • 57. [Deficiency of erythrocytic catalase activity in the city of Puebla, Mexico (author's transl)].
    Saldívar AA, Díaz Carrasco RM, Ruiz Reyes G.
    Rev Invest Clin; 1974 Jan 27; 26(1):47-52. PubMed ID: 4453675
    [No Abstract] [Full Text] [Related]

  • 58. [Alpha1-antitrypsin deficiency, Pi groups and chronic bronchopneumopathy].
    Vidal J, Cazal P, Robinet-Levy M, Michel FB.
    Presse Med (1893); 1970 Apr 04; 78(17):783-6. PubMed ID: 5439754
    [No Abstract] [Full Text] [Related]

  • 59. [Reagin asthma and familial alpha 1 antitrypsin deficiency].
    Bruttmann G.
    Nouv Presse Med; 1974 Mar 09; 3(10):589-91. PubMed ID: 4545038
    [No Abstract] [Full Text] [Related]

  • 60. [Prenatal diagnosis of inborn errors of metabolism. 155 cases (author's transl)].
    Boué J, Nicolas H, Cheruy C, Couillin P, Boué A.
    Nouv Presse Med; 1982 Mar 20; 11(13):979-83. PubMed ID: 7070985
    [Abstract] [Full Text] [Related]

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