136 related articles for article (PubMed ID: 5289034)
21. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
Heyne K; Shin YS; Schwinger E
Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
[TBL] [Abstract][Full Text] [Related]
22. Polymorphism of erythrocyte galactose-1-phosphate uridyl-transferase in Italy: segregation analysis in 693 families.
Vaccaro AM; Mandara I; Muscillo M; Ciaffoni F; De Pellegrin S; Benincasa A; Novelletto A; Terrenato L
Hum Hered; 1984; 34(4):197-206. PubMed ID: 6090305
[TBL] [Abstract][Full Text] [Related]
23. [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]
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. Galactose-1-phosphate uridyltransferase and galactokinase activity in cultured human diploid fibroblasts and peripheral blood leukocytes. I. Analysis of transferase genotypes by the ratio of the activities of the two enzymes.
Tedesco TA; Mellman WJ
J Clin Invest; 1969 Dec; 48(12):2390-7. PubMed ID: 5355349
[TBL] [Abstract][Full Text] [Related]
26. Loss of transferase enzyme activity of transfused erythrocytes in galactosemia.
Schwartz RP; Roesel RA; Blankenship PR; Hall WK
South Med J; 1975 Mar; 68(3):301-2. PubMed ID: 1118770
[TBL] [Abstract][Full Text] [Related]
27. Evaluation of reduced activity galactose-1-phosphate uridyl transferase by combined radioisotopic assay and high-resolution isoelectric focusing.
Kelley RI; Segal S
J Lab Clin Med; 1989 Aug; 114(2):152-6. PubMed ID: 2546999
[TBL] [Abstract][Full Text] [Related]
28. The molecular relationship between deficient UDP-galactose uridyl transferase (GALT) and ceramide galactosyltransferase (CGT) enzyme function: a possible cause for poor long-term prognosis in classic galactosemia.
Lebea PJ; Pretorius PJ
Med Hypotheses; 2005; 65(6):1051-7. PubMed ID: 16125333
[TBL] [Abstract][Full Text] [Related]
29. A new variant of galactosemia: galactose-1-phosphate uridylytransferase sensitive to product inhibition by glucose 1-phosphate.
Lang A; Groebe H; Hellkuhl B; von Figura K
Pediatr Res; 1980 May; 14(5):729-34. PubMed ID: 6247691
[TBL] [Abstract][Full Text] [Related]
30. Problems in the diagnosis of transferase and galactokinase deficient galactosemia.
Pesce MA; Bodourian SH
Ann Clin Lab Sci; 1980; 10(1):26-32. PubMed ID: 7362195
[TBL] [Abstract][Full Text] [Related]
31. Interallelic complementation in hybrid cells derived from Chinese hamster diploid clones deficient in hypoxanthine-guanine phosphoribosyl-transferase activity.
Sekiguchi T; Sekiguchi F
Exp Cell Res; 1973 Mar; 77(1):391-403. PubMed ID: 4570359
[No Abstract] [Full Text] [Related]
32. 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]
33. [Determination of galactose-1-phosphate uridyl transferase in capillary blood in galactosemia. Use in family examinations].
Colombo JP; Moser H; Rosin S; Richterich R; Rossi E
Klin Wochenschr; 1965 Oct; 43(20):1074-81. PubMed ID: 5866779
[No Abstract] [Full Text] [Related]
34. Simultaneous amplification, detection, and analysis of common mutations in the galactose-1-phosphate uridyl transferase gene.
Jama M; Nelson L; Pont-Kingdon G; Mao R; Lyon E
J Mol Diagn; 2007 Nov; 9(5):618-23. PubMed ID: 17884932
[TBL] [Abstract][Full Text] [Related]
35. Partial galactose-1-phosphate uridyltransferase deficiency due to a variant enzyme.
Gitzelmann R; Poley JR; Prader A
Helv Paediatr Acta; 1967 Jul; 22(3):252-7. PubMed ID: 5590140
[No Abstract] [Full Text] [Related]
36. Uridine diphosphoglucose pyrophosphorylase and uridine diphosphogalactose pyrophosphorylase in human skin fibroblasts derived from normal and galactosemic individuals.
Chacko CM; McCrone L; Nadler HL
Biochim Biophys Acta; 1972 Apr; 268(1):113-20. PubMed ID: 5018270
[No Abstract] [Full Text] [Related]
37. [Correction of the symptoms of hereditary galactosemia in W/SSM strain rats by enzymatic imprinting].
Salganik RI; Solov'eva NA; Kandaurov VV
Genetika; 1982 Mar; 18(3):428-33. PubMed ID: 7200439
[TBL] [Abstract][Full Text] [Related]
38. [Galactosemia: a hereditary galactose intolerance].
Sychlowy A
Pediatr Pol; 1972 Jul; 47(7):901-6. PubMed ID: 4559957
[No Abstract] [Full Text] [Related]
39. Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) gene.
Tyfield L; Reichardt J; Fridovich-Keil J; Croke DT; Elsas LJ; Strobl W; Kozak L; Coskun T; Novelli G; Okano Y; Zekanowski C; Shin Y; Boleda MD
Hum Mutat; 1999; 13(6):417-30. PubMed ID: 10408771
[TBL] [Abstract][Full Text] [Related]
40. [Galactosemia].
Grodzka Z; Zbieg-Sendecka E
Probl Med Wieku Rozwoj; 1979; 8():70-6. PubMed ID: 263529
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
