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 *

123 related articles for article (PubMed ID: 290838)

  • 1. [Enzymatic analysis for the diagnosis of inborn errors of carbohydrate metabolism].
    Kusunoki T; Soyama K; Oya N; Kinugasa A
    Nihon Rinsho; 1979 Jun; Suppl():1619-23. PubMed ID: 290838
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M; Moatti N; Lemonnier A
    Ann Biol Clin (Paris); 1979; 37(5):259-70. PubMed ID: 232826
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Reagent that restores galactose-1-phosphate uridylyltransferase activity in dry blood spots.
    Berry HK; Croft CC
    Clin Chem; 1987 Aug; 33(8):1471-2. PubMed ID: 3038378
    [No Abstract]   [Full Text] [Related]  

  • 5. The use of glucose-1-[32P]phosphate for the determination of hexose-1-phosphate uridyl transferase activity in red blood cells.
    Grodzka Z; Chojnacki T
    Biochem Med; 1976 Dec; 16(3):182-6. PubMed ID: 1016259
    [No Abstract]   [Full Text] [Related]  

  • 6. The glycogenoses and other inherited disorders of carbohydrate metabolism.
    Senior B; Sadeghi-Nejad A
    Clin Perinatol; 1976 Mar; 3(1):79-98. PubMed ID: 182428
    [No Abstract]   [Full Text] [Related]  

  • 7. [Diagnostic problems of hereditary intolerance to fructose in young infants].
    Odievre M
    Arch Fr Pediatr; 1969 Jan; 26(1):5-19. PubMed ID: 5254366
    [No Abstract]   [Full Text] [Related]  

  • 8. Enzymatic micromethod for measuring galactose-1-phosphate uridylyltransferase activity in human erythrocytes.
    Pesce MA; Bodourian SH; Harris RC; Nicholson JF
    Clin Chem; 1977 Sep; 23(9):1711-7. PubMed ID: 890916
    [No Abstract]   [Full Text] [Related]  

  • 9. [Importance of the culture of cells in vitro for the diagnosis and study of metabolic diseases].
    Esposito G
    Pediatria (Napoli); 1971; 79(2):270-83. PubMed ID: 4255382
    [No Abstract]   [Full Text] [Related]  

  • 10. [Galactose 1-phosphate level in children with various types of hexosephosphate uridylyltransferase deficiency].
    Grodzka Z; Zbieg-Sendecka E; Mańkowski T
    Pediatr Pol; 1985 Sep; 60(9):631-7. PubMed ID: 3008074
    [No Abstract]   [Full Text] [Related]  

  • 11. Disorders of carbohydrate metabolism.
    Howanitz PJ; Howanitz JH
    Clin Lab Med; 1981 Jun; 1(2):419-32. PubMed ID: 7049524
    [No Abstract]   [Full Text] [Related]  

  • 12. Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurement.
    Shin-Buehring YS; Schaub J
    Clin Chim Acta; 1980 Sep; 106(2):231-4. PubMed ID: 6250747
    [No Abstract]   [Full Text] [Related]  

  • 13. [Current problems in liver and bile duct diseases in childhood. 2].
    Gudowski G; Tambor U; Laske G
    Z Arztl Fortbild (Jena); 1976 Aug; 70(15):825-30. PubMed ID: 1068600
    [No Abstract]   [Full Text] [Related]  

  • 14. Study of a family with Los Angeles, Duarte, and classical galactosemia variants of galactose-1-phosphate uridyl transferase.
    Applegarth DA; Donnell GN; Mullinger M; Ng WG; Lowry AB
    Biochem Med; 1976 Apr; 15(2):206-11. PubMed ID: 962903
    [No Abstract]   [Full Text] [Related]  

  • 15. Inborn errors of carbohydrate metabolism.
    Mayatepek E; Hoffmann B; Meissner T
    Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):607-18. PubMed ID: 20955963
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A preliminary study of the electrophoresis of nucleoside phosphorylase, 2,3-diphosphoglycerate mutase, triosephosphate isomerase and galctose-1-uridyle transferase: technical notes.
    Kishimoto S; Iwasaki Y; Tsuchihashi Y; Daitoku K; Yamada T
    Hiroshima J Med Sci; 1976 Mar; 25(1):63-72. PubMed ID: 135747
    [No Abstract]   [Full Text] [Related]  

  • 17. Fructose I,6 diphosphatase deficiency.
    Tarlow MJ; Patrick AD; Carlton DR; Barton ME
    Proc Nutr Soc; 1979 Dec; 38(3):111A. PubMed ID: 231259
    [No Abstract]   [Full Text] [Related]  

  • 18. [Clinical and pathobiochemical findings in genetic diseases of carbohydrate and lipid metabolism].
    Beyreiss K
    Zentralbl Pathol; 1992 Jun; 138(3):154-67. PubMed ID: 1525131
    [No Abstract]   [Full Text] [Related]  

  • 19. Human erythrocyte galactose-1-phosphate uridylyltransferase. Evidence for a uridylyl-enzyme intermediate by kinetic and exchange reaction studies.
    Markus HB; Wu JW; Boches FS; Tedesco TA; Mellman WJ; Kallen RG
    J Biol Chem; 1977 Aug; 252(15):5363-9. PubMed ID: 889611
    [No Abstract]   [Full Text] [Related]  

  • 20. [SOME NOTIONS ON INBORN ERRORS OF CARBOHYDRATE METABOLISM].
    LUST M
    Scalpel (Brux); 1963 Oct; 116():835-45. PubMed ID: 14096212
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.