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.
49. Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia. Woo HC; Phornphutkul C; Laptook AR J Perinatol; 2010 Apr; 30(4):295-7. PubMed ID: 20351709 [TBL] [Abstract][Full Text] [Related]
50. [A family with galactosemia and "Duarte variant"]. Haschemian G; Menne F Humangenetik; 1972; 15(3):223-6. PubMed ID: 5082089 [No Abstract] [Full Text] [Related]
51. A patient with hereditary galactosemia studied with a screening method for galactose in urine. Dahlqvist A; Jagenburg R; Mark A Acta Paediatr Scand; 1969 May; 58(3):237-44. PubMed ID: 4977384 [No Abstract] [Full Text] [Related]
52. Erythrocyte galactose-1-phosphate uridyl transferase activity in infants of low birth weight. Beitner R; Reisner SH; Pinsky A; Levi I Isr J Med Sci; 1969; 5(1):27-32. PubMed ID: 5796278 [No Abstract] [Full Text] [Related]
53. [Galactose-uridyl-transferase deficit in a patient with trisomy 21]. Agosti E Quad Sclavo Diagn; 1972 Mar; 8(1):199-203. PubMed ID: 4663751 [No Abstract] [Full Text] [Related]
54. Galactosemia screening of newborns in Massachusetts. Shih VE; Levy HI; Karolkewicz V; Houghton S; Efron ML; Isselbacher KJ; Beutler E; MacCready RA N Engl J Med; 1971 Apr; 284(14):753-7. PubMed ID: 4926707 [No Abstract] [Full Text] [Related]
55. 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]
56. [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]
57. Interallelic complementation in hybrid cells derived from human diploid strains deficient in galactose-1-phosphate uridyl transferase activity. Nadler HL; Chacko CM; Rachmeler M Proc Natl Acad Sci U S A; 1970 Oct; 67(2):976-82. PubMed ID: 5289034 [TBL] [Abstract][Full Text] [Related]
58. [Hereditary galactosemia in rats: biochemical mechanisms of the disease]. Solov'eva NA; Kandaurov VA; Zaĭdman AM; Salganik RI Vopr Med Khim; 1982; 28(3):15-21. PubMed ID: 6213094 [TBL] [Abstract][Full Text] [Related]