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Journal Abstract Search

170 related items for PubMed ID: 5425825

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  • 5. [The family of a patient with galactokinase-defect 2nd communication (author's transl)].
    Kaloud H, Sitzmann FC, Paltauf F, Mayer R.
    Klin Padiatr; 1974 Jan; 186(1):33-6. PubMed ID: 4365835
    [No Abstract] [Full Text] [Related]

  • 6. Galactokinase deficiency in twins: clinical and biochemical studies.
    Olambiwonnu NO, McVie R, Ng WG, Frasier SD, Donnell GN.
    Pediatrics; 1974 Mar; 53(3):314-8. PubMed ID: 4360930
    [No Abstract] [Full Text] [Related]

  • 7. [Study of the utilization of galactose injected intra-venous in the premature, the newborn and young cildren].
    Lestradet H, Gentil M, Prochorow M, Tichet J.
    Arch Fr Pediatr; 1969 Mar; 26(6):621-31. PubMed ID: 5802057
    [No Abstract] [Full Text] [Related]

  • 8. Galactose metabolism in the newborn infant.
    Donnell GN, Ng WG, Hodgman JE, Bergren WR.
    Pediatrics; 1967 Jun; 39(6):829-37. PubMed ID: 6026549
    [No Abstract] [Full Text] [Related]

  • 9. The inherited defects of erythrocyte metabolism.
    Fornaini G, Bossu M.
    Ital J Biochem; 1969 Jun; 18(4):185-326. PubMed ID: 4243574
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  • 10. Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studies.
    Benson PF, Brown SP, Cree J, Fensom AH, Grant AR.
    Birth Defects Orig Artic Ser; 1976 Jun; 12(3):305-12. PubMed ID: 182297
    [Abstract] [Full Text] [Related]

  • 11. A patient with hereditary galactokinase deficiency.
    Dahlqvist A, Gamstorp I, Madsen H.
    Acta Paediatr Scand; 1970 Nov; 59(6):669-75. PubMed ID: 5482251
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  • 12. Galactokinase-deficiency cataracts in identical twins.
    Oberman AE, Wilson WA, Frasier SD, Donnell GN, Bergren WR.
    Am J Ophthalmol; 1972 Nov; 74(5):887-92. PubMed ID: 4644736
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [Galactokinase defect in a newborn infant].
    Linneweh F, Schaumlöffel E, Vetrella M.
    Klin Wochenschr; 1970 Jan 01; 48(1):31-3. PubMed ID: 5522111
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  • 15. Hypergalactosemia and galactosuria due to galactokinase deficiency in a newborn.
    Thalhammer O, Gitzelmann R, Pantlitschko M.
    Pediatrics; 1968 Sep 01; 42(3):441-5. PubMed ID: 5695665
    [No Abstract] [Full Text] [Related]

  • 16. [Familial diphosphoglycerate mutase deficiency: hematological and biochemical study].
    Cartier P, Labie D, Leroux JP, Najman A, Demaugre F.
    Nouv Rev Fr Hematol; 1972 Sep 01; 12(3):269-87. PubMed ID: 4266202
    [No Abstract] [Full Text] [Related]

  • 17. [An unusual form of galactose metabolism disorder].
    Rubecz I, Ritecz E, Méhes K, Csordás J.
    Orv Hetil; 1971 Dec 19; 112(51):3051-4. PubMed ID: 5136647
    [No Abstract] [Full Text] [Related]

  • 18. [Clinical and biochemical findings in a child with hereditary galactokinase defect].
    Kaloud H, Sitzmann FC, Mayer R, Paltauf F.
    Klin Padiatr; 1973 Jan 19; 185(1):18-22. PubMed ID: 4734834
    [No Abstract] [Full Text] [Related]

  • 19. Galactose metabolism in a patient with hereditary galactokinase deficiency.
    Gitzelmann R, Wells HJ, Segal S.
    Eur J Clin Invest; 1974 Apr 19; 4(2):79-84. PubMed ID: 4365005
    [No Abstract] [Full Text] [Related]

  • 20. Some inferences from galactokinase deficiency.
    Sidbury JB.
    Pediatrics; 1974 Mar 19; 53(3):309-10. PubMed ID: 4360929
    [No Abstract] [Full Text] [Related]

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