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7. [HEREDITARY INTOLERANCE TO FRUCTOSE]. ROYER P; LESTRADET H; HABIB R; LARDINOIS R; DESBUQUOIS B Bull Mem Soc Med Hop Paris; 1964 Jun 5-12; 115():805-23. PubMed ID: 14186900 [No Abstract] [Full Text] [Related]
8. [CARBOHYDRATE METABOLISM DISORDERS CAUSED BY ENZYME DEFICIENCIES]. CHMIELOWA M Pol Arch Med Wewn; 1964; 34():1359-65. PubMed ID: 14273186 [No Abstract] [Full Text] [Related]
9. 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]
10. STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME. HSIA DY; INOUYE T; WONG P; SOUTH A N Engl J Med; 1964 May; 270():1085-8. PubMed ID: 14121488 [No Abstract] [Full Text] [Related]
11. ENZYMES IN MENTAL RETARDATION. II. ROSANOVA AR; NEIMEYER H; COMPALL T; MICHAELSON AS IMJ Ill Med J; 1964 Sep; 126():335-41. PubMed ID: 14199874 [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. ERYTHROCYTIC GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE LEVELS IN HEPATIC CIRRHOSIS. FISHER MM; SPEAR S; SAMOLS E; SHERLOCK S Gut; 1964 Apr; 5(2):170-2. PubMed ID: 14159408 [No Abstract] [Full Text] [Related]
14. [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]
15. Biochemical properties of human red cell galactose-1-phosphate uridyl transferase (UDP glucose: alpha-D-galactose-1-phosphate uridyltransferase E.C.2.7.7.12) from normal and mutant subjects. Beutler E; Baluda MC; Halasz A J Lab Clin Med; 1966 Jun; 67(6):947-54. PubMed ID: 5916143 [No Abstract] [Full Text] [Related]
16. [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]
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. Human galactose 1-phosphate uridyltransferase. Purification, antibody production, and comparison of the wild type, Duarte variant, and galactosemic gene products. Tedesco TA J Biol Chem; 1972 Oct; 247(20):6631-6. PubMed ID: 4627742 [No Abstract] [Full Text] [Related]
19. [Determination of galactose-1-phosphate-uridyl-transferase activity in children with galactosemia and their relatives]. Knapp W; Winkler G Padiatr Grenzgeb; 1972; 11(1):35-47. PubMed ID: 5042112 [No Abstract] [Full Text] [Related]
20. [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] [Next] [New Search]