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Journal Abstract Search
322 related items for PubMed ID: 568459
1. 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 [Abstract] [Full Text] [Related]
7. [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 [Abstract] [Full Text] [Related]
8. Estimation of amniotic cell galactose-1-phosphate uridyltransferase for prenatal diagnosis of galactosemia in Taiwan. Chen SC, Chu WC, Yang ML, Ng HT. Taiwan Yi Xue Hui Za Zhi; 1984 Jan; 83(1):113-8. PubMed ID: 6327878 [No Abstract] [Full Text] [Related]
16. [Efficacy of dietetic treatment in a case of galactosemia diagnosed late]. Sebastio G, Albini F, di Martino L, Magurno T, Baffa E, Ciaffoni F. Pediatr Med Chir; 1982 Jun; 4(6):685-6. PubMed ID: 6927423 [Abstract] [Full Text] [Related]
19. A new variant of galactosemia: galactose-1-phosphate uridylytransferase sensitive to product inhibition by glucose 1-phosphate. Lang A, Groebe H, Hellkuhl B, von Figura K. Pediatr Res; 1980 May; 14(5):729-34. PubMed ID: 6247691 [Abstract] [Full Text] [Related]
20. [Late diagnosis of classical galactosemia. An adult with special biochemistry]. Weits-Binnerts JJ, Hordijk R, Smit GP, van der Veer E, Reijngoud DJ, Berger R. Tijdschr Kindergeneeskd; 1993 Oct; 61(5):188-90. PubMed ID: 8266315 [Abstract] [Full Text] [Related] Page: [Next] [New Search]