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 *

148 related articles for article (PubMed ID: 5784816)

  • 1. [Galactosemia: 14C galactose metabolism in blood cells. Application to the detection of heterozygotes].
    Tron P; Milhaud G
    Rev Fr Etud Clin Biol; 1969 Jan; 14(1):12-8. PubMed ID: 5784816
    [No Abstract]   [Full Text] [Related]  

  • 2. Galactose metabolism by the mouse with galactose-1-phosphate uridyltransferase deficiency.
    Ning C; Reynolds R; Chen J; Yager C; Berry GT; McNamara PD; Leslie N; Segal S
    Pediatr Res; 2000 Aug; 48(2):211-7. PubMed ID: 10926297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterozygous state of galactosemia with clinical signs of the disease?
    Ionăşescu V; Luca N
    J Genet Hum; 1969 May; 17(1):53-64. PubMed ID: 5808540
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Pathways of galactose metabolism by galactosemics: evidence for galactose conversion to hepatic UDPglucose.
    Segal S; Wehrli S; Yager C; Reynolds R
    Mol Genet Metab; 2006 Feb; 87(2):92-101. PubMed ID: 16260165
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Galactose metabolism and its regulation.
    Cohn RM; Segal S
    Metabolism; 1973 Apr; 22(4):627-42. PubMed ID: 4348859
    [No Abstract]   [Full Text] [Related]  

  • 7. [Correction of the symptoms of hereditary galactosemia in W/SSM strain rats by enzymatic imprinting].
    Salganik RI; Solov'eva NA; Kandaurov VV
    Genetika; 1982 Mar; 18(3):428-33. PubMed ID: 7200439
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Biochemical mechanisms of the development of hereditary galactosemia in W/SSM strain rats].
    Solov'eva NA; Salganik RI
    Genetika; 1982 Mar; 18(3):420-7. PubMed ID: 7200438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Studies on a family with galactosemia].
    von Berg W
    Dtsch Med Wochenschr; 1969 Jan; 94(2):61-5. PubMed ID: 5782691
    [No Abstract]   [Full Text] [Related]  

  • 10. [Galactosemia: detection of galactokinase deficiency].
    Klethi J
    C R Seances Soc Biol Fil; 1973; 167(6):1048-51. PubMed ID: 4371918
    [No Abstract]   [Full Text] [Related]  

  • 11. [Clinical and morphological findings in during galactosemia].
    Roschlau G; Hinkel GK; Gottschalk B
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):7-13. PubMed ID: 5407995
    [No Abstract]   [Full Text] [Related]  

  • 12. [Galactosemia: detection of galactose-phosphate-uridyltransferase deficiency].
    Klethi J
    C R Seances Soc Biol Fil; 1973; 167(10):1461-6. PubMed ID: 4793567
    [No Abstract]   [Full Text] [Related]  

  • 13. [Galactosemia: a hereditary galactose intolerance].
    Sychlowy A
    Pediatr Pol; 1972 Jul; 47(7):901-6. PubMed ID: 4559957
    [No Abstract]   [Full Text] [Related]  

  • 14. [Detection of heterozygotes of galactosemia].
    Camus B; Farriaux JP; Fontaine G
    Ann Biol Clin (Paris); 1968; 26(10):1223-32. PubMed ID: 4387236
    [No Abstract]   [Full Text] [Related]  

  • 15. [Metabolically conditioned forms of imbecility and their diagnosis. II. Galactosemia].
    Grümer HD
    Z Klin Chem Klin Biochem; 1966 May; 4(3):123-6. PubMed ID: 4296924
    [No Abstract]   [Full Text] [Related]  

  • 16. Human UDP-galactose 4' epimerase (GALE) gene and identification of five missense mutations in patients with epimerase-deficiency galactosemia.
    Maceratesi P; Daude N; Dallapiccola B; Novelli G; Allen R; Okano Y; Reichardt J
    Mol Genet Metab; 1998 Jan; 63(1):26-30. PubMed ID: 9538513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detection of galactosemia in heterozygotes].
    László A; Zoltán H; Havass Z
    Orv Hetil; 1979 Aug; 120(32):1931-4. PubMed ID: 503460
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. Galactose utilization in galactosemia.
    Petricciani JC; Binder MK; Merril CR; Geier MR
    Science; 1972 Mar; 175(4028):1368-70. PubMed ID: 5059566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.