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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. Galactose-1-phosphate uridyl transferase in fibroblasts: isozymes in normal and variant states. Hammersen G; Mandell R; Levy HL Ann Hum Genet; 1975 Oct; 39(2):147-50. PubMed ID: 1052762 [TBL] [Abstract][Full Text] [Related]
25. Polymorphism of human galactose-1-phosphate uridyl transferase. Mulley JC Hum Hered; 1982; 32(1):42-5. PubMed ID: 6279487 [TBL] [Abstract][Full Text] [Related]
26. Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers. Murphy M; McHugh B; Tighe O; Mayne P; O'Neill C; Naughten E; Croke DT Eur J Hum Genet; 1999 Jul; 7(5):549-54. PubMed ID: 10439960 [TBL] [Abstract][Full Text] [Related]
27. Cataracts related to enzymes of galactose metabolism. Schoon DV Metab Pediatr Ophthalmol; 1981; 5(3-4):219-23. PubMed ID: 6273670 [No Abstract] [Full Text] [Related]
28. Development of a protocol for newborn screening for disorders of the galactose metabolic pathway. Bowling FG; Brown AR J Inherit Metab Dis; 1986; 9(1):99-104. PubMed ID: 3014213 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. [Premature ovarian failure in galactosaemia: pathophysiology and clinical management]. Forges T; Monnier-Barbarino P Pathol Biol (Paris); 2003 Feb; 51(1):47-56. PubMed ID: 12628293 [TBL] [Abstract][Full Text] [Related]
31. Galactose-1-phosphate uridylyltransferase activity in chronic lymphocytic leukemia. Johnson LD Cancer Biochem Biophys; 1979; 3(2):75-9. PubMed ID: 233300 [TBL] [Abstract][Full Text] [Related]
32. Regulation of galactose metabolism: implications for therapy. Segal S; Rogers S J Inherit Metab Dis; 1990; 13(4):487-500. PubMed ID: 2122115 [TBL] [Abstract][Full Text] [Related]
34. Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiency. Vaca G; Sanchez-Corona J; Medina C; Olivares N; Rivera H; Hernández A; Ibarra B; Sotomayor JM; Cantú JM Arch Invest Med (Mex); 1978; 9(3):477-84. PubMed ID: 568459 [TBL] [Abstract][Full Text] [Related]
35. Galactose-1 phosphate uridyl transferase deficiency in the western grey kangaroo (Macropus fuliginosus; marsupialia): a model system for gene therapy studies. Richardson BJ; Inglis B; Poole WE; Rolfe B Aust J Exp Biol Med Sci; 1979 Feb; 57(1):43-9. PubMed ID: 383061 [TBL] [Abstract][Full Text] [Related]
36. Comparison of galactose-1-phosphate uridyl transferase in fetal and adult tissues. Hammersen G; Levy HL; Frigoletto F; Mandell R Clin Chim Acta; 1975 May; 60(3):281-4. PubMed ID: 1139775 [TBL] [Abstract][Full Text] [Related]
37. Association of presenile cataracts with heterozygosity for galactosaemic states and with riboflavin deficiency. Prchal JT; Conrad ME; Skalka HW Lancet; 1978 Jan; 1(8054):12-3. PubMed ID: 74495 [TBL] [Abstract][Full Text] [Related]
38. [Identification of inborn errors of galactose metabolism in patients with cataracts]. Vaca-Pacheco G; Medina C; García-Cruz D; Sánchez-Corona J; Chávez-Anaya E; Jaimes C; Hernández-Córdova A Arch Invest Med (Mex); 1990; 21(2):127-32. PubMed ID: 2103700 [TBL] [Abstract][Full Text] [Related]
39. Impaired hexose uptake by diploid skin fibroblasts from galactosaemic patients. Connection with cell growth and amino acid metabolism, and possible bearing on late-onset clinical symptoms. Wolfrom C; Raynaud N; Kadhom N; Poggi J; Soni T; Gautier M J Inherit Metab Dis; 1993; 16(1):78-90. PubMed ID: 8098071 [TBL] [Abstract][Full Text] [Related]
40. Galactose-1-phosphate uridyl transferase in density-fractionated erythrocytes. Studies of normal and mutant enzymes. Kelley RI; Feinberg DM; Segal S Hum Genet; 1989 May; 82(2):99-103. PubMed ID: 2542154 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]