These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 6276048)

  • 21. Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia.
    Sitzmann FC; Kaloud H
    Clin Chim Acta; 1976 Nov; 72(3):343-51. PubMed ID: 184990
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Galactosemia: alterations in sulfate metabolism secondary to galactose-1-phosphate uridyltransferase deficiency.
    Tedesco TA; Miller KL
    Science; 1979 Sep; 205(4413):1395-7. PubMed ID: 472754
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Pathological findings in galactosemia caused by a galactose-1-phosphaturidyltransferase defect (author's transl)].
    Gathmann HA
    Klin Padiatr; 1977 Mar; 189(2):177-84. PubMed ID: 558474
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locus.
    Christensen E; Brandt NJ
    J Inherit Metab Dis; 1978; 1(4):167-9. PubMed ID: 117252
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A new method of screening for inherited disorders of galactose metabolism.
    Paigen K; Pacholec F; Levy HL
    J Lab Clin Med; 1982 Jun; 99(6):895-907. PubMed ID: 7042875
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human galactose 1-phosphate uridylyltransferase. Absence of half-reaction activity of galactosemic proteins.
    Wu JW; Tedesco TA; Kallen RG; Mellman WJ
    J Biol Chem; 1974 Nov; 249(21):7038-9. PubMed ID: 4214116
    [No Abstract]   [Full Text] [Related]  

  • 27. Inexplicable infantile cataracts and partial maternal galactose disorder.
    Brivet M; Abadie V; Soni T; Cheron G; Dufier JL
    Arch Dis Child; 1986 May; 61(5):445-8. PubMed ID: 3013103
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Deficit of uridine diphosphate galactose in galactosaemia.
    Ng WG; Xu YK; Kaufman FR; Donnell GN
    J Inherit Metab Dis; 1989; 12(3):257-66. PubMed ID: 2515367
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Borderline galactosemia.
    Pettersson R; Dahlqvist A; Hattevig G; Kjellman B
    Acta Paediatr Scand; 1980 Nov; 69(6):735-9. PubMed ID: 7211358
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurement.
    Shin-Buehring YS; Schaub J
    Clin Chim Acta; 1980 Sep; 106(2):231-4. PubMed ID: 6250747
    [No Abstract]   [Full Text] [Related]  

  • 31. Microdetermination of galactose and galactose 1-phosphate in dried blood spots.
    Fujimura Y; Ishii S; Kawamura M; Naruse H
    Anal Biochem; 1981 Oct; 117(1):187-95. PubMed ID: 7316189
    [No Abstract]   [Full Text] [Related]  

  • 32. The use of a radioisotopic method for estimation of galactose-1-phosphate in galactosemia.
    Bozkowa K; Duchnowska A
    Biochem Med; 1977 Feb; 17(1):24-30. PubMed ID: 843340
    [No Abstract]   [Full Text] [Related]  

  • 33. [Galactosemia and cow's milk intolerance (author's transl)].
    Gómez de Terreros I; Gayoso Gómez F; Senín Sánchez J; Castro Gómez A; Muñóz Conde J; de la Rosa A
    An Esp Pediatr; 1978 Feb; 11(2):157-64. PubMed ID: 655510
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M; Moatti N; Lemonnier A
    Ann Biol Clin (Paris); 1979; 37(5):259-70. PubMed ID: 232826
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Preliminary results of UDP galactose pyrophosphorylase in the erythrocytes of healthy persons and in patients with galactosaemia.
    Mańkowski T; Radomyska B; Zbieg-Sendecka E
    Mater Med Pol; 1990; 22(3):191-3. PubMed ID: 2132425
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts.
    Friedman TB; Yarkin RJ; Merril CR
    J Cell Physiol; 1975 Jun; 85(3):569-78. PubMed ID: 167035
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Radiochemical assay of minute quantities of galactose-1-phosphate uridyltransferase activity in erythrocytes and leukocytes of galactosemia patients.
    Xu YK; Kaufman FR; Donnell GN; Ng WG
    Clin Chim Acta; 1995 Mar; 235(2):125-36. PubMed ID: 7554267
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Galactosemia and its prenatal diagnosis].
    Wiśniewski L; Wrede A
    Ginekol Pol; 1978 Dec; 49(12):1097-103. PubMed ID: 748104
    [No Abstract]   [Full Text] [Related]  

  • 39. Study of a family with both galactosemic and Duarte variants of galactose-1-phospho uridyl transferase.
    Schapira F; Gregori C; Poenaru L
    Biochem Med; 1974 Sep; 11(1):87-92. PubMed ID: 4415964
    [No Abstract]   [Full Text] [Related]  

  • 40. [The frequency of uridyl transferase deficiency in patients with galactose intolerance].
    Fernekorn A; Fiehring C
    Dtsch Gesundheitsw; 1976 Dec; 31(52):2455-60. PubMed ID: 1009846
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.