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27. [Problems of phenotypic similarity and differential diagnostic of hereditary diseases in children]. Barashnev IuI Vestn Akad Med Nauk SSSR; 1982; (6):47-51. PubMed ID: 7051616 [No Abstract] [Full Text] [Related]
28. [Studies on lipid metabolism in childhood. On the significance of lecithin: cholesterol fatty acyl transferase determination in various child liver diseases]. Imamura S Sapporo Igaku Zasshi; 1968; 34(2):90-8. PubMed ID: 5753282 [No Abstract] [Full Text] [Related]
29. [Study of the alkaline phophatase and 5-nucleotidase activity of the serum. Clinical and experimental results]. Housset E; Etienne JP ETITE JP Rev Int Hepatol; 1967 May; 17(6):519-36. PubMed ID: 5585947 [No Abstract] [Full Text] [Related]
30. [Hereditary intolerance to fructose]. Mariani R; Siino A; Richert J; Bernard R Mars Med; 1969; 106(2):127-43. PubMed ID: 5768598 [No Abstract] [Full Text] [Related]
31. Therapy in congenital hyperbilirubinemia: phenobarbital and diethylnicotinamide. Ertel IJ; Newton WA Pediatrics; 1969 Jul; 44(1):43-8. PubMed ID: 5795402 [No Abstract] [Full Text] [Related]
32. [Intestinal disaccharidases enzyme activity. Its reduction in enteropathy caused by gluten and in other conditions of malabsorption]. De Larrechea I; Sampayo RR; Sosa Miatello C; Ibarra R Prensa Med Argent; 1966 Jul; 53(26):1421-5. PubMed ID: 5999675 [No Abstract] [Full Text] [Related]
33. [Hereditary fructose intolerance]. Vaisman N; Cooper M; Garti R Harefuah; 1981 May; 100(10):464-6. PubMed ID: 7308886 [No Abstract] [Full Text] [Related]
34. [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]
35. [Congenital disorders of carbohydrate metabolism in children]. Rosenkranz A Wien Med Wochenschr; 1965 Nov; 115(45):953-7. PubMed ID: 5221113 [No Abstract] [Full Text] [Related]
37. [Determination of blood serum 5'-nucleotidase activity in differential diagnosis of jaundice]. Braginskiĭ DM; Paktoris EA; Sinaĭko GA; Shakhgil'ian IV Sov Med; 1980; (6):49-52. PubMed ID: 6251570 [No Abstract] [Full Text] [Related]
38. 'In vitro' assay of bilirubin-UDP glucuronyl transferase activity in the liver of patients with Gilbert's syndrome and a variety of hepatic disorders. Black M; Billing BH Gut; 1968 Dec; 9(6):728-9. PubMed ID: 5717986 [No Abstract] [Full Text] [Related]
39. [Serum 5'nucleotidases: experimental and clinical study]. Pappo E; Christoforov B; Petite JP; Boulu R; Etienne JP; Housset E Actual Hepatogastroenterol (Paris); 1969; 5(7):B289+. PubMed ID: 5378655 [No Abstract] [Full Text] [Related]
40. [Hereditary fructose intolerance. Early manifestation in newborns and young infants (author's transl)]. Vieweg B; Posselt HG; Streb H; Strobel S Monatsschr Kinderheilkd; 1982 Jan; 130(1):21-6. PubMed ID: 7062914 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]