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25. Early cataract formation due to galactokinase deficiency: impact of newborn screening. Janzen N; Illsinger S; Meyer U; Shin YS; Sander J; Lücke T; Das AM Arch Med Res; 2011 Oct; 42(7):608-12. PubMed ID: 22154682 [TBL] [Abstract][Full Text] [Related]
26. Galactose metabolism in mice with galactose-1-phosphate uridyltransferase deficiency: sucklings and 7-week-old animals fed a high-galactose diet. Ning C; Reynolds R; Chen J; Yager C; Berry GT; Leslie N; Segal S Mol Genet Metab; 2001 Apr; 72(4):306-15. PubMed ID: 11286504 [TBL] [Abstract][Full Text] [Related]
27. [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]
28. Ultra fast and sensitive liquid chromatography tandem mass spectrometry based assay for galactose-1-phosphate uridylyltransferase and galactokinase deficiencies. Li Y; Ptolemy AS; Harmonay L; Kellogg M; Berry GT Mol Genet Metab; 2011 Jan; 102(1):33-40. PubMed ID: 20863731 [TBL] [Abstract][Full Text] [Related]
29. [Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism]. Kadhom N; Brivet M; Baptista J; Gautier M; Lemonnier A C R Acad Sci III; 1989; 308(17):453-8. PubMed ID: 2543487 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies. Levy HL; Sepe SJ; Walton DS; Shih VE; Hammersen G; Houghton S; Beutler E J Pediatr; 1978 Mar; 92(3):390-3. PubMed ID: 632977 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. [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]
35. Multiplex enzyme assay for galactosemia using ultraperformance liquid chromatography-tandem mass spectrometry. Ko DH; Jun SH; Park HD; Song SH; Park KU; Kim JQ; Song YH; Song J Clin Chem; 2010 May; 56(5):764-71. PubMed ID: 20299679 [TBL] [Abstract][Full Text] [Related]
37. Galactose and cataract. Stambolian D Surv Ophthalmol; 1988; 32(5):333-49. PubMed ID: 3043741 [TBL] [Abstract][Full Text] [Related]
38. Plasma galactose and galactitol concentration in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia: determination by gas chromatography/mass spectrometry. Ning C; Segal S Metabolism; 2000 Nov; 49(11):1460-6. PubMed ID: 11092512 [TBL] [Abstract][Full Text] [Related]
39. [Determination of galactose-1-phosphate-uridyl-transferase activity in children with galactosemia and their relatives]. Knapp W; Winkler G Padiatr Grenzgeb; 1972; 11(1):35-47. PubMed ID: 5042112 [No Abstract] [Full Text] [Related]
40. Erythrocyte Galactose-1-phosphate measurement by GC-MS in the monitoring of classical galactosemia. Cangemi G; Barco S; Barbagallo L; Di Rocco M; Paci S; Giovannini M; Biasucci G; Lia R; Melioli G Scand J Clin Lab Invest; 2012 Feb; 72(1):29-33. PubMed ID: 22017166 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]