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]