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.
8. Genetic studies in galactosemia. I. The oral galactose tolerance test and the heterozygous state. DONNELL GN; BERGREN WR; ROLDAN M Pediatrics; 1959 Sep; 24():418-26. PubMed ID: 13817544 [No Abstract] [Full Text] [Related]
10. 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]
11. Galactosemia, a case presentation. HAYES MS J Christ Med Assoc India; 1955 May; 30(3):115-6. PubMed ID: 13242643 [No Abstract] [Full Text] [Related]
12. [Galactosemia; death despite supression of dietary galactose]. MONNET P; LARBRE F; COTTE J; TISSOT A Pediatrie; 1959; 14(1):63-6. PubMed ID: 13633382 [No Abstract] [Full Text] [Related]
13. Congenital galactosemia, a single enzymatic block in galactose metabolism. ISSELBACHER KJ; ANDERSON EP; KURAHASHI K; KALCKAR HM Science; 1956 Apr; 123(3198):635-6. PubMed ID: 13311516 [No Abstract] [Full Text] [Related]
16. [Galactosemia or galactose diabetes]. ROMANI L Clin Nuova Rass Prog Med Int; 1954 Jun; 18(11):521-4. PubMed ID: 13199905 [No Abstract] [Full Text] [Related]
17. Detection of congenital galactosemia and the carrier state using galactose C14 and blood cells. WEINBERG AN Metabolism; 1961 Sep; 10():728-34. PubMed ID: 14005688 [No Abstract] [Full Text] [Related]