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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

321 related articles for article (PubMed ID: 568459)

  • 1. 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]  

  • 2. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K; Shin YS; Schwinger E
    Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Prenatal diagnosis of galactose-1-phosphate uridyltransferase (GALT)-deficient galactosemia.
    Elsas LJ
    Prenat Diagn; 2001 Apr; 21(4):302-3. PubMed ID: 11288121
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. [Investigation of the frequency of heterozygotes for galactose-1-phosphate-uridyl-transferase-deficiency(galactosemia) in the Vienna area. Comparison with the frequency of homozygotes found by newborn screening (author's transl)].
    Scheibenreiter S; Scheiber V; Kiefer A
    Padiatr Padol; 1976; 11(1):305-12. PubMed ID: 1250629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Estimation of amniotic cell galactose-1-phosphate uridyltransferase for prenatal diagnosis of galactosemia in Taiwan.
    Chen SC; Chu WC; Yang ML; Ng HT
    Taiwan Yi Xue Hui Za Zhi; 1984 Jan; 83(1):113-8. PubMed ID: 6327878
    [No Abstract]   [Full Text] [Related]  

  • 9. Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia.
    Sitzmann FC; Kaloud H
    Clin Chim Acta; 1976 Nov; 72(3):343-51. PubMed ID: 184990
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variants.
    Andersen MW; Williams VP; Sparkes MC; Sparkes RS
    Hum Genet; 1984; 65(3):287-90. PubMed ID: 6321325
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Genetic basis of galactosemia.
    Reichardt JK
    Hum Mutat; 1992; 1(3):190-6. PubMed ID: 1301925
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of galactosemia.
    Schapira F; Gregori C; Boué J; Henrion R; Vigneron C; Vidailhet M
    Biomedicine; 1978 Jun; 29(4):136-8. PubMed ID: 687757
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [Screening for galactose-1-phosphate uridyltransferase deficiency (classic galactosemia) in newborns].
    Ahlbehrendt I; Wagenknecht C
    Acta Biol Med Ger; 1977; 36(5-6):797-800. PubMed ID: 602584
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. A new variant of galactosemia: galactose-1-phosphate uridylytransferase sensitive to product inhibition by glucose 1-phosphate.
    Lang A; Groebe H; Hellkuhl B; von Figura K
    Pediatr Res; 1980 May; 14(5):729-34. PubMed ID: 6247691
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 17.