Genetic disease since 1945 (original) (raw)

References

  1. Rosenberg, C. & Golden, J. (eds) Framing Disease: Studies in Cultural History (Rutgers Univ. Press, New Brunswick, New Jersey, 1992).
    Book Google Scholar
  2. Epstein, S. Impure Science: AIDS, Activism, and the Politics of Knowledge (Berkeley, Univ. of California Press, 1996).
    Google Scholar
  3. Aronowitz, R. Making Sense of Illness: Science, Society and Disease (Cambridge Univ. Press, Cambridge, 1998).
    Google Scholar
  4. Jacobs Brumberg, J. Fasting Girls: The Emergence of Anorexia Nervosa as a Modern Disease (Harvard Univ. Press, Cambridge, Massachusetts, 1988).
    Google Scholar
  5. McKusick, V. The growth and development of human genetics as a clinical discipline. Am. J. Hum. Genet. 27, 261–273 (1975).
    CAS PubMed PubMed Central Google Scholar
  6. Axelrod, F. B., Porges, R. F. & Sein, M. E. Neonatal recognition of familial dysautonomia. J. Pediatr. 110, 946–948 (1987).
    Article CAS Google Scholar
  7. Riley, C. M. A short history of Familial dysautonomia. A report to the Dysautonomia Foundation 19 November (1979).
    Google Scholar
  8. Riley, C. M., Day, R. L., Greeley, D. M. & Langford, W. S. Central autonomic dysfunction with defective lacrimation: report of five cases . Pediatrics 3, 468–481 (1949).
    CAS PubMed Google Scholar
  9. The Dysautonomia treatment and Evaluation Center at NYU Medical Center, Genesis: Newsletter of the Genetics Network of the Empire State 11, (New York State Department of Health, 1980).
  10. Axelrod, F. Familial dysautonomia: Manual of Comprehensive Care (Dysautonomia Foundation, New York, 1997).
    Book Google Scholar
  11. Guzzetta, F., Tortorella, G., Cardia, E. & Ferriere, G. Familial dysautonomia in a non-Jewish girl. Dev. Med. Child Neurol. 28, 62–68 ( 1986).
    Article CAS Google Scholar
  12. Brunt, P. W. & McKusick, V. A. Familial dysautonomia: A report of genetic and clinical studies, with a review of the literature. Medicine 49, 343–374 ( 1970).
    Article CAS Google Scholar
  13. Blumenfeld, A. et al. Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genet. 4, 160–164 ( 1993).
    Article CAS Google Scholar
  14. Yoxen, E. in The Problem of Medical Knowledge: Examining the Social Construction of Medicine (eds Wright, P. & Treacher, A.) 144–161 (Edinburgh Univ. Press, Edinburgh, 1982).
    Google Scholar
  15. Hormuth, R. P. United States Children's Bureau, to M. Beaudet, 6 December 1965, 20–212 1963–1966, Box 1097, NN3–102, Records of the U. S. Children's Bureau, Central File, RG 102, National Archives and Records Administration, Washington, D. C.
  16. Scriver, C. R. Whatever happened to PKU? Clin. Biochem. 28, 137–144 (1995).
    Article CAS Google Scholar
  17. Faden, R. R., Holtzman, N. & Chwalow, J. Parental rights, child welfare and public health: the case of PKU screening. Am. J. Public Health 72, 1396–1400 (1982).
    Article CAS Google Scholar
  18. Bessman, S. & Swazey, J. in Human Aspects of Biomedical Innovation (eds Mendelsohn, E. et al.) 49–76 (Harvard Univ. Press, Cambridge, Massachusetts, 1971).
    Google Scholar
  19. Paul, D. & Edelson, P. J. in Molecularizing Biology and Medicine: New Practices and Alliances, 1910s–1970s (eds de Chadarevian, S. & Kamminga, H.) 203–220 (Harwood Academic, Reading, 1998).
    Book Google Scholar
  20. Committee for the Study of Inborn Errors of Metabolism in Genetic Screening: Programs, Principles and Research 92 –93 (Natl Acad. Sci., Washington DC, 1975).
  21. Folling, A. Phenylpyruvic acid as a metabolic anomaly in connection with imbecility. Nord. Med. Tidskr. 8, 1054–1059 (1934). (A paper with the same title also appeared in the German Zeitschrift fur Physiologische Chemie 227, 169–176 (1934).)
    Google Scholar
  22. Louis, W. & Vulliamy, D. B. Phenylketonuria with a study of the effect upon it of glutamic acid. Arch. Dis. Childh. 26, 487–494 (1951).
    Article Google Scholar
  23. Bickel, H. Gerrard, J. & Hickmans, E. M. Influence of phenylalanine intake on phenylketonuria . Lancet 2, 812–813 (1953).
    Article Google Scholar
  24. Blumenfield, A. et al. Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on chromosome 9q31. Am. J. Hum. Genet. 64, 1110–1118 (1999).
    Article Google Scholar
  25. Porter, I. in Maxcy–Rosenau Public Health and Preventive Medicine 11th Edn (ed. Last, J. M.) 1375–1422 (Appleton-Century–Crofts, New York, 1980).
    Google Scholar
  26. Knoppers, B. M. in New Horizons in Neonatal Screening (eds Farriaux, J. P. & Dhondt, J.-L.) 257–277 (Proc. Ninth Int. Neonatal Screening Symposium and the Second Meeting of the Int. Soc. for Neonatal Screening, Lille, France, 13–17 September 1993).
    Google Scholar
  27. McKusick, V. The growth and development of human genetics as a clinical discipline. Am. J. Hum. Genet. 27, 261–273 (1975).
    CAS PubMed PubMed Central Google Scholar

Download references