Hostname: page-component-848d4c4894-r5zm4 Total loading time: 0 Render date: 2024-06-28T15:05:30.656Z Has data issue: false hasContentIssue false
  • English
  • Français

The dietary treatment of inborn errors of metabolism

Published online by Cambridge University Press:  28 February 2007

L. I. Woolf
L. I. Woolf
Affiliation:
Kinsmen Laboratory of Neurological Research, Department of Psychiatry, University of British Columbia, Vancouver V6T 1W5, British Columbia, Canada
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
Meeting Report
Information
Proceedings of the Nutrition Society , Volume 35 , Issue 1 , May 1976 , pp. 31 - 36
Copyright
Copyright © The Nutrition Society 1976

References

Allan, J. D. & Brown, J. K. (1968). In Symposium on Some Recent Advances in Inborn Errors of Metabolism, p. 14 [Holt, K. S. and Coffey, V. P., editors]. Edinburgh: Livingstone.Google Scholar
Arakawa, T. (1970). Am. J. Med. 48, 594.CrossRefGoogle Scholar
Armstrong, M. D. & Tyler, F. H. (1955). J. clin. Invest. 34, 565.Google Scholar
Arthur, L. J. H. & Hulme, J. D. (1970). Pediatrics, Springfield 46, 235.CrossRefGoogle Scholar
Auerbach, V. H. & Di George, A. M. (1973). In Inborn Errors of Metabolism, p. 337 [Hommes, F. A. and van den Berg, C. J., editors]. London and New York: Academic Press.Google Scholar
Baumeister, A. A. (1967). Am. J. ment. Defic. 71, 840.Google Scholar
Bickel, H. (1967). In Phenylketonuria and Allied Metabolic Diseases, p. 177 [Anderson, J. A. and Swaiman, K. F., editors]. Washington, DC: US Government Printing Office.Google Scholar
Bickel, H., Gerrard, J. & Hickmans, E. M. (1953). Lancet ii, 812.CrossRefGoogle Scholar
Bickel, H., Hudson, F. P. & Woolf, L. I. (editors) (1971). Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism. Stuttgart: Thieme Verlag.Google Scholar
Bruhl, H. H. (editor) (1966). Symposium on Nutrition and Inherited Diseases of Man as Related to Public Health. Minneapolis: Minnesota Department of Health.Google Scholar
Coates, S. (1961). Br. med. J. i, 767.Google Scholar
Crome, L., Tymms, V. & Woolf, L. I. (1962). J. Neurol. Neurosurg. Psychiat. 25, 143.Google Scholar
Dahlqvist, A. & Asp, N.-G. (1975). Biochem. Soc. Trans. 3, 227.Google Scholar
Dent, C. E. & Westall, R. G. (1961). Archs Dis. Childh. 36, 259.Google Scholar
Fisch, R. O. & Anderson, J. A. (1971). In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 73 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Fischler, K. (1971). In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 213 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Holzel, A. (1962). In Erbliche Stoffwechselkrankheiten, p. 219 [Linneweh, F., editor]. Munich: Urban and Schwarzenberg.Google Scholar
Howell, R. R. & Stevenson, R. E. (1971). Social Biol. 18, S19.Google Scholar
Hsia, D. Y.-Y. (editor) (1969). Galactosemia. Springfield, Illinois: C. C. Thomas.Google Scholar
Hudson, F. P. (1971). In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 273 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Hudson, F. P. & Hawcroft, J. (1973). In Treatment of Inborn Errors of Metabolism, p. 51 [Seakins, J. W. T., Saunders, R. A. and Toothill, C., editors]. Edinburgh and London: Churchill Livingstone.Google Scholar
Kalckar, H. M., Kinoshita, J. H. & Donnell, G. N. (1973). In Biology of Brain Dysfunction, vol. 1, p. 31 [Gaull, G. E., editor]. New York: Plenum Press.CrossRefGoogle Scholar
Knox, W. E. (1972). In The Metabolic Basis of Inherited Disease, 3rd ed., p. 266 [Stanbury, J. B., Wyngaarden, J. B. and Fredrickson, D. S., editors]. New York: McGraw-Hill.Google Scholar
Koch, R., Dobson, J. C., Blaskovics, M., Williamson, M. L., Ernest, A. E., Friedman, E. G. & Parker, C. E. (1973). In Treatment of Inborn Errors of Metabolism p. 3 [Seakins, J. W. T., Saunders, R. A. and Toothill, C., editors]. Edinburgh and London: Churchill Livingstone.Google Scholar
Luhby, A. L., Eagle, F. J.. Roth, E. & Cooperman, J. M. (1961). Am. J. Dis. Child. 102, 482.Google Scholar
McBean, M. S. In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 280 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Mackenzie, D. Y. & Woolf, L. I. (1959). Br. med. J. i, 9.Google Scholar
Mudd, S. H., Uhlendorf, B. W., Freeman, J. M., Finkelstein, J. D. & Shih, V. E. (1972). Biochem. biophys. Res. Commun. 46, 905.Google Scholar
Murphy, D. (1963). Ir. J. med. Sci. 6, 355.Google Scholar
Murphy, D. (1969). Ir. J. med. Sci. 8, 177.Google Scholar
Partington, M. W. (1971). In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 26 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Prader, A. & Auricchio, S. (1965). A. Rev. Med. 16, 345.CrossRefGoogle Scholar
Rosenberg, L. E. & Mahoney, M. J. (1973). In Inborn Errors of Metabolism, p. 303 [Hommens, F. A. and van den Berg, C. J., editors]. London and New York: Academic Press.Google Scholar
Seriver, C. R., Mackenzie, S., Clow, C. L. & Delvin, E. (1971). Lancet i, 310.Google Scholar
Segal, S. (1972). In The Metabolic Basis of Inherited Disease, 3rd ed., p. 174 [Stanbury, J. B., Wyngaarden, J. B. and Fredrickson, D. S., editors]. New York: McGraw-Hill.Google Scholar
Snyderman, S. E. (1971). In Phenylketonuria and Some Other Inborn Errors of Amino Acid Metabolism, p. 283 [Bickel, H., Hudson, F. P. and Woolf, L. I., editors]. Stuttgart: Thieme Verlag.Google Scholar
Solomons, G., Keleske, L. & Opitz, E. (1966). J. Pediat. 69, 596.CrossRefGoogle Scholar
Walters, T. R. (1967). J. Pediat. 70, 686.Google Scholar
Woolf, L. I. (1962). Adv. clin. Chem. 5, 1.Google Scholar
Woolf, L. I. (1973). In Treatment of Inborn Errors of Metabolism, p. 57 [Seakins, J. W. T., Saunders, R. A. and Toothill, C., editors]. Edinburgh and London: Churchill Livingstone.Google Scholar
Woolf, L. I., Griffiths, R. & Moncrieff, A. A. (1955). Br. med. J. i, 57.Google Scholar
Woolf, L. I., Griffiths, R., Moncrieff, A. A., Coates, S. & Dillistone, F. (1958). Archs Dis. Childh. 33, 31.Google Scholar
Woolf, L. I. & Vulliamy, D. (1951). Archs Dis. Childh. 26, 487.CrossRefGoogle Scholar