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5. 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]
6. [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]
7. Stable-isotope dilution analysis of galactose metabolites in human erythrocytes. Schadewaldt P; Kamalanathan L; Hammen HW; Wendel U Rapid Commun Mass Spectrom; 2003; 17(24):2833-8. PubMed ID: 14673834 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Impaired NADPH oxidase activity in peripheral blood lymphocytes of galactosemia patients. Al-Essa M; Dhaunsi GS; Al-Qabandi W; Khan I Exp Biol Med (Maywood); 2013 Jul; 238(7):779-86. PubMed ID: 23828587 [TBL] [Abstract][Full Text] [Related]
11. Biochemical changes and clinical outcomes in 34 patients with classic galactosemia. Yuzyuk T; Viau K; Andrews A; Pasquali M; Longo N J Inherit Metab Dis; 2018 Mar; 41(2):197-208. PubMed ID: 29350350 [TBL] [Abstract][Full Text] [Related]
12. Outcomes of siblings with classical galactosemia. Hughes J; Ryan S; Lambert D; Geoghegan O; Clark A; Rogers Y; Hendroff U; Monavari A; Twomey E; Treacy EP J Pediatr; 2009 May; 154(5):721-6. PubMed ID: 19181333 [TBL] [Abstract][Full Text] [Related]
13. Serum markers of bone turnover in children and adolescents with classic galactosemia. Gajewska J; Ambroszkiewicz J; Radomyska B; Chełchowska M; Ołtarzewski M; Laskowska-Klita T; Milanowski A Adv Med Sci; 2008; 53(2):214-20. PubMed ID: 18650146 [TBL] [Abstract][Full Text] [Related]
14. Galactosemia in Thai patient at Phramongkutklao Hospital: a case report. Boonyawat B; Kamolsilp M; Phavichitr N J Med Assoc Thai; 2005 Nov; 88 Suppl 3():S275-80. PubMed ID: 16858969 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Transient galactosemia detected by neonatal mass screening. Ono H; Mawatari H; Mizoguchi N; Eguchi T; Sakura N; Hamakawa M Pediatr Int; 1999 Jun; 41(3):281-4. PubMed ID: 10365579 [TBL] [Abstract][Full Text] [Related]
17. [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]
18. Methionine/galactose ratio on newborn blood spots useful for reduction of false positives for homocystinuria and galactosemia by high-performance anion-exchange chromatography with pulsed amperometric detection. Lee JY; Sim HJ; Kwon HJ; Lee YM; Yoon HR; Hong SP Clin Chim Acta; 2012 Jan; 413(1-2):182-6. PubMed ID: 21951896 [TBL] [Abstract][Full Text] [Related]
19. A new method of screening for inherited disorders of galactose metabolism. Paigen K; Pacholec F; Levy HL J Lab Clin Med; 1982 Jun; 99(6):895-907. PubMed ID: 7042875 [TBL] [Abstract][Full Text] [Related]
20. Microassay for screening newborns for galactosemia with use of a fluorometric microplate reader. Yamaguchi A; Fukushi M; Mizushima Y; Shimizu Y; Takasugi N; Arashima S; Ohyanagi K Clin Chem; 1989 Sep; 35(9):1962-4. PubMed ID: 2776326 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]