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Journal Abstract Search
125 related items for PubMed ID: 204112
1. [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 06; 90(1):16-20. PubMed ID: 204112 [Abstract] [Full Text] [Related]
2. [Pathobiochemistry of galactosemia and usefulness of the Gt system in expert opinions (author's transl)]. Berg K, Schwarzfischer F, Wischerath H. Med Klin; 1975 Nov 14; 70(46):1881-2. PubMed ID: 1186586 [Abstract] [Full Text] [Related]
4. [Identification of inborn errors of galactose metabolism in patients with cataracts]. Vaca-Pacheco G, Medina C, García-Cruz D, Sánchez-Corona J, Chávez-Anaya E, Jaimes C, Hernández-Córdova A. Arch Invest Med (Mex); 1990 Nov 14; 21(2):127-32. PubMed ID: 2103700 [Abstract] [Full Text] [Related]
5. [Critical comments on the isotope test for galactokinase and galactose-1-P-uridyltransferase using the DE-81-filter paper]. Osang M, Schaub J. Monatsschr Kinderheilkd (1902); 1975 May 14; 123(5):484-5. PubMed ID: 176579 [No Abstract] [Full Text] [Related]
10. [Screening of newborns for inborn errors of galactose metabolism. Methods and results]. Gitzelmann R. Monatsschr Kinderheilkd (1902); 1976 Sep 14; 129(9):654-7. PubMed ID: 185513 [Abstract] [Full Text] [Related]
11. [The galactokinase deficiency in two human populations: Styria (Austria) and Franconia (Bavaria). A comparative investigation on gen frequency (author's transl)]. Kaloud H, Sitzmann FC. Z Kinderheilkd; 1974 Feb 11; 116(3):185-91. PubMed ID: 4360413 [No Abstract] [Full Text] [Related]
12. Galactokinase deficiency as a cause of cataracts. Beutler E, Matsumoto F, Kuhl W, Krill A, Levy N, Sparkes R, Degnan M. N Engl J Med; 1973 Jun 07; 288(23):1203-6. PubMed ID: 4700553 [No Abstract] [Full Text] [Related]
13. Excretion of galactitol in the urine of heterozygotes of both forms of galactosemia. Sitzmann FC, Schmid RD, Kaloud H. Clin Chim Acta; 1977 Mar 01; 75(2):313-9. PubMed ID: 191219 [Abstract] [Full Text] [Related]
15. [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)]. Thalhammer O, Scheibenreiter S, Knoll E, Wehle E. Klin Padiatr; 1980 Nov 01; 192(6):613-9. PubMed ID: 6452554 [Abstract] [Full Text] [Related]
16. [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 Nov 01; 25(5):257-62. PubMed ID: 6091357 [No Abstract] [Full Text] [Related]
17. Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase. Allerdice PW, Tedesco TA. Lancet; 1975 Jul 05; 2(7923):39. PubMed ID: 49636 [No Abstract] [Full Text] [Related]