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29. Defect in uptake of galactose-1-phosphate into liver nucleotides in congenital galactosemia. ANDERSON EP; ISSELBACHER KJ; KALCKAR HM Science; 1957 Jan; 125(3238):113-4. PubMed ID: 13390971 [No Abstract] [Full Text] [Related]
30. Galactosemia in an eight day old infant. SMITH FM J La State Med Soc; 1955 Feb; 107(2):49-52. PubMed ID: 13233668 [No Abstract] [Full Text] [Related]
34. Galactosemia. A family study. CHRISTIAN JR; DIAMOND EF Am J Dis Child; 1961 Jan; 101():75-7. PubMed ID: 13693393 [No Abstract] [Full Text] [Related]
35. [Diagnosis and therapy of galactosemia and phenylketonuria]. BICKEL H Monatsschr Kinderheilkd (1902); 1955 Feb; 103(2):81-4. PubMed ID: 14383678 [No Abstract] [Full Text] [Related]
36. Amino-aciduria in galactosemia. YI-YUNG HSIA D; HSIA HH; GREEN S; KAY M; GELLIS SS AMA Am J Dis Child; 1954 Oct; 88(4):458-65. PubMed ID: 13196667 [No Abstract] [Full Text] [Related]
37. Studies on the heterozygous carrier in galactosemia. HUANG I; HUGH-JONES K; HSIA DY J Lab Clin Med; 1959 Oct; 54():585-92. PubMed ID: 14403637 [No Abstract] [Full Text] [Related]
38. Galactosemia, a congenital defect in a nucleotide transferase. KALCKAR HM; ANDERSON EP; ISSELBACHER KJ Biochim Biophys Acta; 1956 Apr; 20(1):262-8. PubMed ID: 13315373 [No Abstract] [Full Text] [Related]