Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-25T19:46:56.094Z Has data issue: false hasContentIssue false
  • English
  • Français

Fructose intolerance: diet and inheritance

Published online by Cambridge University Press:  28 February 2007

Timothy M Cox
Timothy M Cox
Affiliation:
Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke' Hospital, Hills Road, Cambridge CB2 2QQ
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Symposium on ‘Health implications of nutrient-gene interactions’
Information
Proceedings of the Nutrition Society , Volume 50 , Issue 2 , August 1991 , pp. 305 - 309
Copyright
The Nutrition Society

References

Chambers, R. A., & Pratt, R. T. C. (1956). Idiosyncrasy to fructose. Lancet ii, 340.CrossRefGoogle Scholar
Cox, T. M. (1988). Hereditary fructose intolerance. Quarterly Journal of Medicine 68, 585–594.Google ScholarPubMed
Cox, T. M. O'Donnell, M. W., Camilleri, M. & Burghes, A. H. (1983). Isolation and characterization of a mutant liver aldolasa it adult hereditary fructose intolerance. Journal of Clinical Investigation 72, 201–213.CrossRefGoogle Scholar
Cross, N. C. P., de Franchis, R., Sehastio, G., Dazzo, C., Tolan, D. R., Gregori, C., Odiévre, M., Vidaihet Romano, C., Musumeci, S., Steinman, B., Gitzemann, R. & Cox, T. M. (1990). Molecular analysis of aldolase B genes in hereditary fructose intocular analysis of aldolasa B genes in hereditary fructose intolerance. Lancet 335, 606–309.CrossRefGoogle Scholar
Cross, N. C. P. Tolan, D. R. & Cox, T. M. (1988). Catalytic deficiency of human aldolase B in hereditary fructose intoerance caused by a common missense mutation. Cell 53, 881–885.CrossRefGoogle ScholarPubMed
Froesch, E. R., Wolf, H. P., Baitsch, H., Prader, A. & Labhart, H. (1963). Hereditary fructose intolerance An inborn defect of fructose-1-phosphate splitting alsolase. American Journal of Medicine 34, 151–167.CrossRefGoogle Scholar
Gitzelmann, R., Steinmann, B. & Van den Berge, G. (1989). Hereditary fructose intolerance. In the Metabolic Basis of Inherited Disease, pp. 399–424 [Scriver, C. R. Beaudet, A. L. Sly, W. S. and Walle, D. editors] New York: McGraw-Hill.Google Scholar
Grégori, C., Shapira, F., Kahn, A., Delpech, M. & Dreyfus, J.-C. (1982). Molecular studies of liver aldolase B in hereditary fructose intolerance using blotting and immunological techniques. Annuls Human Genetics 46, 281–292.CrossRefGoogle ScholarPubMed
Hers, H.-G. & Joassin, G. (1961). Anomalie de I'aldolase hepatique dans I'intolerance au fructose. (An anomaly in hepatic aldolase during fructose intolerance). Enzymologia Biologicu Clinica 1, 4–14.CrossRefGoogle Scholar
Nordmann, Y., Shapira, F., & Dreyfus, J. -C.. (1968). A structurally modified liver aldolase in hereditary fructose intolerance: Immunological and kinetic evidence. Biochemical and Biophysical Research Communications 31, 884–889.CrossRefGoogle ScholarPubMed
Odiévre, M., Gentil, C. Gautier, M. & Alagille, D. (1978). Hereditary fructose intolerance in childhood: diagnosisi, Managemetn and course in 55 patients. American Journal of Diseases of Children 132, 605–608.CrossRefGoogle Scholar
Tolan, D. R. & Penhoet, E. E. (1986). Characterization of the human aldolase B gene. Molecular Biology and Medicine 3, 245–264.Google ScholarPubMed