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23. Haemorrhagic diathesis as a possible early sign of hereditary fructose intolerance. Hosková A, Mrskos A. Eur J Pediatr; 1977 Dec 30; 127(1):63-5. PubMed ID: 606560 [Abstract] [Full Text] [Related]
24. [Diagnostic procedures in hereditary fructose intolerance (author's transl)]. Thanner F. Klin Wochenschr; 1977 Aug 15; 55(16):787-90. PubMed ID: 904245 [Abstract] [Full Text] [Related]
25. Pseudodominant transmission of fructose intolerance in an adult and three offspring: Heterozygote detection by intestinal biopsy. Cox TM, Camilleri M, O'Donnell MW, Chadwick VS. N Engl J Med; 1982 Aug 26; 307(9):537-40. PubMed ID: 7099225 [No Abstract] [Full Text] [Related]
26. Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intolerance. Gitzelmann R, Steinmann B, Bally C, Lebherz HG. Biochem Biophys Res Commun; 1974 Aug 19; 59(4):1270-7. PubMed ID: 4212946 [No Abstract] [Full Text] [Related]
34. Fanconi's syndrome in an adult. A case history. Naidoo PM. S Afr Med J; 1975 Jul 19; 49(31):1269-72. PubMed ID: 239454 [Abstract] [Full Text] [Related]
35. [Case of defibrination syndrome in an infant presenting with hereditary intolerance to fructose]. Lebranchu Y, Seigneurin D, Rambaud P, Kolodie L. Pediatrie; 1976 Jul 19; 31(4):389-97. PubMed ID: 958790 [No Abstract] [Full Text] [Related]
36. An experimental renal acidification defect in patients with hereditary fructose intolerance. II. Its distinction from classic renal tubular acidosis; its resemblance to the renal acidification defect associated with the Fanconi syndrome of children with cystinosis. Morris RC. J Clin Invest; 1968 Jul 19; 47(7):1648-63. PubMed ID: 5658593 [Abstract] [Full Text] [Related]
37. Possible role of thiol groups in the abnormal kinetics of aldolase in hereditary fructose intolerance. Lemonnier F, Gregori C, Schapira F. Biochem Biophys Res Commun; 1974 Nov 06; 61(1):306-12. PubMed ID: 4441399 [No Abstract] [Full Text] [Related]