These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
210 related articles for article (PubMed ID: 6927423)
1. [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]
2. [Clinical and biochemical diagnosis of galactosemia among our cases]. Bozkowa K; Zbieg-Sendecka E; Grodzka Z; Cabalska B Probl Med Wieku Rozwoj; 1979; 8():63-9. PubMed ID: 263527 [TBL] [Abstract][Full Text] [Related]
3. 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]
6. 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]
7. [From gene to disease; galactosemia and galactose-1-phosphate uridyltransferase deficiency]. Bosch AM; Waterham HR; Bakker HD Ned Tijdschr Geneeskd; 2004 Jan; 148(2):80-1. PubMed ID: 14753129 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. [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]
10. 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]
11. [Galactosemia]. Grodzka Z; Zbieg-Sendecka E Probl Med Wieku Rozwoj; 1979; 8():70-6. PubMed ID: 263529 [TBL] [Abstract][Full Text] [Related]
12. [Late diagnosis of classical galactosemia. An adult with special biochemistry]. Weits-Binnerts JJ; Hordijk R; Smit GP; van der Veer E; Reijngoud DJ; Berger R Tijdschr Kindergeneeskd; 1993 Oct; 61(5):188-90. PubMed ID: 8266315 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients. Mirzajani F; Mirfakhraie R; Nabati F; Tabatabaei NN; Talachian E; Houshmand M Clin Biochem; 2006 Jul; 39(7):697-9. PubMed ID: 16765930 [TBL] [Abstract][Full Text] [Related]