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29. [Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption]. Nüssli R Helv Paediatr Acta; 1971 Dec; 26(5):637-47. PubMed ID: 5142943 [No Abstract] [Full Text] [Related]
30. Glucose-galactose malabsorption. Report of a case with autoradiographic studies of a mucosal biopsy. Schneider AJ; Kinter WB; Stirling CE N Engl J Med; 1966 Feb; 274(6):305-12. PubMed ID: 5903212 [No Abstract] [Full Text] [Related]
31. [Infantile scurvy in glucose-galactose malabsorption]. Majewski A; Burdelski M; Hampel V Rontgenblatter; 1982 Dec; 35(12):447-9. PubMed ID: 7178769 [No Abstract] [Full Text] [Related]
32. Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene. Atay FY; Derme T; Uras N; Ceylaner G; Ceylaner S; Sari FN; Oguz SS Dig Dis Sci; 2017 Jan; 62(1):280-281. PubMed ID: 27783308 [No Abstract] [Full Text] [Related]
34. Congenital glucose-galactose malabsorption: A rare and severe cause of infant diarrhea. Pascual Pérez AI; Martínez Velasco S; García Volpe C Med Clin (Barc); 2019 May; 152(10):e55-e56. PubMed ID: 30409526 [No Abstract] [Full Text] [Related]
36. Direct and maternal aspects of the risk of cataract with partial disorders of galactose metabolism. Winder AF; Fielder AR; Mount JN; Menzies JS Clin Genet; 1985 Sep; 28(3):199-206. PubMed ID: 4064358 [TBL] [Abstract][Full Text] [Related]