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23. 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]
24. Fruit flies and milk sugar. Harrington M Lab Anim (NY); 2010 Jul; 39(7):196. PubMed ID: 20567220 [No Abstract] [Full Text] [Related]
25. Komrower Lecture. Galactosaemia today: the enigma and the challenge. Segal S J Inherit Metab Dis; 1998 Aug; 21(5):455-71. PubMed ID: 9728327 [No Abstract] [Full Text] [Related]
26. Another aspect of the galactosemia enigma. Segal S Mol Genet Metab; 2004 Mar; 81(3):253-4; author reply 255-7. PubMed ID: 14972332 [No Abstract] [Full Text] [Related]
27. Galactose metabolism in transferase-deficient galactosaemic and normal long-term lymphoid cell lines. Beratis NG; Wilbur L J Inherit Metab Dis; 1987; 10(4):347-58. PubMed ID: 2831430 [TBL] [Abstract][Full Text] [Related]
28. [Classical galactosemia and the Duarte variant of transferase in a family]. Jurcić Z; Dogan K; Rudar D; Lipovac K; Cepelak I Acta Med Iugosl; 1978; 32(1):93-101. PubMed ID: 645435 [No Abstract] [Full Text] [Related]
29. Failure to identify heterozygotes for galactosaemia in women with premature ovarian failure. Fraser IS; Shearman RP; Wilcken B; Brown A; Davis K Lancet; 1987 Sep; 2(8558):566. PubMed ID: 2887854 [No Abstract] [Full Text] [Related]
33. Spontaneous pregnancy in a patient with classical galactosaemia. de Jongh S; Vreken P; IJst L; Wanders RJ; Jakobs C; Bakker HD J Inherit Metab Dis; 1999 Aug; 22(6):754-5. PubMed ID: 10472536 [No Abstract] [Full Text] [Related]
34. [Gene frequencies of both forms of galactosaemia in the western Hungarian province of Vas (author's transl)]. Sitzmann FC; Istvan L; Teubl I; Kaloud H; Cholnoky P Wien Klin Wochenschr; 1978 Jan; 90(1):16-20. PubMed ID: 204112 [TBL] [Abstract][Full Text] [Related]
35. Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency. Maceratesi P; Sangiuolo F; Novelli G; Ninfali P; Magnani M; Reichardt JK; Dallapiccola B Hum Mutat; 1996; 8(4):369-72. PubMed ID: 8956044 [No Abstract] [Full Text] [Related]
36. Of mice and men: galactosemia. Segal S Mol Genet Metab; 2006 Dec; 89(4):401-2. PubMed ID: 16914342 [No Abstract] [Full Text] [Related]
37. [Determination of reference ranges for the activity of galactose-1-phosphate uridyltransferase (E.C. 2.7.7.12) in the blood using a simple optimized method of determination and comparison with the results of a half-quantitative screening method]. Ahlbehrendt I; Wagenknecht C Z Med Lab Diagn; 1984; 25(5):257-62. PubMed ID: 6091357 [No Abstract] [Full Text] [Related]
38. Pregnancy and delivery after stimulation with rFSH of a galatosemia patient suffering hypergonadotropic hypogonadism: case report. Menezo YJ; Lescaille M; Nicollet B; Servy EJ J Assist Reprod Genet; 2004 Mar; 21(3):89-90. PubMed ID: 15202737 [TBL] [Abstract][Full Text] [Related]
39. [Galactosemia; variability in clinical aspects and problems in the diagnosis]. van Wijk-Hoek JM; de Klerk JB; Cats BP; Gerards LJ; van der Heiden C Ned Tijdschr Geneeskd; 1985 Sep; 129(38):1836-40. PubMed ID: 2997633 [No Abstract] [Full Text] [Related]
40. Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase. Allerdice PW; Tedesco TA Lancet; 1975 Jul; 2(7923):39. PubMed ID: 49636 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]