BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 602584)

  • 1. [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]  

  • 2. [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]  

  • 3. [Galactosemia caused by galactosephosphate uridylyltransferase].
    Lachmajer-Lutosławska M; Hoppe A
    Pediatr Pol; 1978 Jan; 53(1):85-8. PubMed ID: 643406
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [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]  

  • 6. Galactosemia: alterations in sulfate metabolism secondary to galactose-1-phosphate uridyltransferase deficiency.
    Tedesco TA; Miller KL
    Science; 1979 Sep; 205(4413):1395-7. PubMed ID: 472754
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. 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]  

  • 9. Galactosemia: a psycho-social perspective.
    Gershen JA
    Ment Retard; 1975 Aug; 13(4):20-3. PubMed ID: 1160608
    [No Abstract]   [Full Text] [Related]  

  • 10. [Galactose-1-phosphate uridyltransferase deficiency].
    Okano Y; Isshiki G
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):15-21. PubMed ID: 9589977
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Cataracts related to enzymes of galactose metabolism.
    Schoon DV
    Metab Pediatr Ophthalmol; 1981; 5(3-4):219-23. PubMed ID: 6273670
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. [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; 192(6):613-9. PubMed ID: 6452554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The diagnosis of galactosemia: screening or clinical diagnosis?].
    Derksen-Lubsen G
    Ned Tijdschr Geneeskd; 1980 Jul; 124(30):1250-6. PubMed ID: 7412896
    [No Abstract]   [Full Text] [Related]  

  • 19. Duarte variant-galactosemia heterozygote. Repository identification No. GM-1996.
    Donnell GN; Ng WG; Alfi OS; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1977; 19(1):53-4. PubMed ID: 891264
    [No Abstract]   [Full Text] [Related]  

  • 20. Newborn screening for galactosemia in Tennessee.
    Ulm JE
    J Tenn Med Assoc; 1992 Nov; 85(11):520-2. PubMed ID: 1434621
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.