BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 872429)

  • 1. Starch gel electrophoresis for galactose-1-phosphate uridylyl-transferase applied to dried filter paper blood specimens.
    Hammersen G; Levy HL
    Clin Chim Acta; 1977 Jun; 77(3):295-9. PubMed ID: 872429
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.
    Bowling FG; Brown AR
    J Inherit Metab Dis; 1986; 9(1):99-104. PubMed ID: 3014213
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Quantitative Beutler test for newborn mass screening of galactosemia using a fluorometric microplate reader.
    Fujimoto A; Okano Y; Miyagi T; Isshiki G; Oura T
    Clin Chem; 2000 Jun; 46(6 Pt 1):806-10. PubMed ID: 10839768
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rennes-like variant of galactosemia: clinical and biochemical studies.
    Hammersen G; Houghton S; Levy HL
    J Pediatr; 1975 Jul; 87(1):50-57. PubMed ID: 1151546
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison of galactose-1-phosphate uridyl transferase in fetal and adult tissues.
    Hammersen G; Levy HL; Frigoletto F; Mandell R
    Clin Chim Acta; 1975 May; 60(3):281-4. PubMed ID: 1139775
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [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; 70(46):1881-2. PubMed ID: 1186586
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular studies on galactose 1 phosphate uridylyl transferase from normal and mutant subjects. An immunological approach.
    Banroques J; Schapira F; Grégori C; Dreyfus JC
    Ann Hum Genet; 1983 Jul; 47(3):177-85. PubMed ID: 6311074
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphism of human galactose-1-phosphate uridyl transferase.
    Mulley JC
    Hum Hered; 1982; 32(1):42-5. PubMed ID: 6279487
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 123(5):484-5. PubMed ID: 176579
    [No Abstract]   [Full Text] [Related]  

  • 11. [Screening of newborns for inborn errors of galactose metabolism. Methods and results].
    Gitzelmann R
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):654-7. PubMed ID: 185513
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal diagnosis of galactosemia.
    Ng WG; Donnell GN; Bergren WR; Alfi O; Golbus MS
    Clin Chim Acta; 1977 Feb; 74(3):227-35. PubMed ID: 188570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. GALT Deficiency Galactosemia.
    Anderson S
    MCN Am J Matern Child Nurs; 2018; 43(1):44-51. PubMed ID: 29215423
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Galactose-1-phosphate uridyl transferase in fibroblasts: isozymes in normal and variant states.
    Hammersen G; Mandell R; Levy HL
    Ann Hum Genet; 1975 Oct; 39(2):147-50. PubMed ID: 1052762
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. A screening procedure and a specific quantitative method for UDPglucose: alpha-D-galactose-1-phosphate uridylyltransferase (EC 2.7.7.12).
    Ibbott FA
    Clin Chem; 1977 Jul; 23(7):1348-55. PubMed ID: 872388
    [No Abstract]   [Full Text] [Related]  

  • 18. Florida newborn screening for galactosemia.
    DeClue TJ; Malone JI; Tedesco TA
    J Fla Med Assoc; 1991 Jun; 78(6):369-71. PubMed ID: 1831492
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Gonadal failure in young women and galactose-1-phosphate uridyl transferase activity.
    Hagenfeldt K; von Döbeln U; Hagenfeldt L
    Fertil Steril; 1989 Jan; 51(1):177-8. PubMed ID: 2535985
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.