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23. Classic galactosemia presenting with unilateral Peters' anomaly. Faras H; Al-Raqum F; Ramadan D Med Princ Pract; 2010; 19(4):324-6. PubMed ID: 20516712 [TBL] [Abstract][Full Text] [Related]
24. On the screening for inborn errors of galactose metabolism. Vaca G; SĂ nchez-Corona J; Olivares N; Medina C; Ibarra B; CantĂș JM Ann Genet; 1983; 26(3):191-2. PubMed ID: 6606384 [TBL] [Abstract][Full Text] [Related]
26. A case of cataract formation during the lactating period associated with galactose-1-phosphate uridyl transferase deficiency. Avisar RA; Schwartzman S; Levinsky H; Allalouf D; Goldman J; Ninio A; Savir H Metab Pediatr Syst Ophthalmol; 1982; 6(1):45-8. PubMed ID: 6290834 [No Abstract] [Full Text] [Related]
27. GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE ASSAY BY USE OF RADIOACTIVE GALACTOSE-1-PHOSPHATE. NG WG; BERGEN WR; DONNELL GN Clin Chim Acta; 1964 Oct; 10():337-43. PubMed ID: 14219578 [No Abstract] [Full Text] [Related]
28. Galactosaemia and the problem of galactose toxicity. Schwarz V Biochem Soc Trans; 1975; 3(2):234-8. PubMed ID: 165990 [No Abstract] [Full Text] [Related]
29. 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]
30. Florida newborn screening for galactosemia. DeClue TJ; Malone JI; Tedesco TA J Fla Med Assoc; 1991 Jun; 78(6):369-71. PubMed ID: 1831492 [TBL] [Abstract][Full Text] [Related]
32. Introduction of newborn screening for galactosemia to Arkansas. West R; Gibson JB J Ark Med Soc; 1996 Mar; 92(10):501-4. PubMed ID: 8867237 [No Abstract] [Full Text] [Related]
33. Abnormal galactosylation of complex carbohydrates in cultured fibroblasts from patients with galactose-1-phosphate uridyltransferase deficiency. Ornstein KS; McGuire EJ; Berry GT; Roth S; Segal S Pediatr Res; 1992 May; 31(5):508-11. PubMed ID: 1603629 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Investigation of the frequency of heterozygotes for galactose-1-phosphate-uridyl-transferase-deficiency(galactosemia) in the Vienna area. Comparison with the frequency of homozygotes found by newborn screening (author's transl)]. Scheibenreiter S; Scheiber V; Kiefer A Padiatr Padol; 1976; 11(1):305-12. PubMed ID: 1250629 [TBL] [Abstract][Full Text] [Related]
36. Estimation of amniotic cell galactose-1-phosphate uridyltransferase for prenatal diagnosis of galactosemia in Taiwan. Chen SC; Chu WC; Yang ML; Ng HT Taiwan Yi Xue Hui Za Zhi; 1984 Jan; 83(1):113-8. PubMed ID: 6327878 [No Abstract] [Full Text] [Related]
37. Newborn screening for galactosemia: a new method used in Manitoba. Greenberg CR; Dilling LA; Thompson R; Ford JD; Seargeant LE; Haworth JC Pediatrics; 1989 Aug; 84(2):331-5. PubMed ID: 2748263 [TBL] [Abstract][Full Text] [Related]
39. [Efficacy of dietetic treatment in a case of galactosemia diagnosed late]. Sebastio G; Albini F; di Martino L; Magurno T; Baffa E; Ciaffoni F Pediatr Med Chir; 1982; 4(6):685-6. PubMed ID: 6927423 [TBL] [Abstract][Full Text] [Related]