LabCAST


SessionReferences
  1. Seeberger, L. Huntington's disease. In Medlink-Neurobase (www.medlink.com), 2nd ed., ed. S. Gilman. 2000. San Diego: Arbor Publishing Corp.
  2. Leavitt, B.R. et al., Clinical and Neuropathological Features of Huntington's Disease. Seminars in Neurology 1999; 19(4).
  3. Riley, D.E. and Lang, A.E. Movement Disorders. In Neurology in Clinical Practice, 3rd ed., Vol II, ed. W.G. Bradley et al., 1889-1930. 2000. Boston: Butterworth-Heinemann.
  4. Leavitt, B.R. et al., Recent Insights From A Human Database of HD Patients. Seminars in Neurology 1999; 19(4).
  5. Rosenblatt, A. et al., Genetics. In A Physician's Guide to the Management of Huntington's Disease, 2nd ed., 9-12. 1999. Huntington's Disease Society of America.
  6. Almqvist, E.W. et al. A Worldwide Assesment of the Frequency of Suicide, Suicide Attempts, or Psychiatric Hospitalization after Predictive Testing for Huntington Disease. American Journal of Human Genetics 1999; 64:1293-1304.
  7. Harper, P.S. and Newcombe, R.G. Age at onset and life table risks in genetic counselling for Huntington's disease. Journal of Medical Genetics 1992; 29:239-242.
  8. Nance, M.A. and the US Huntington's Disease Genetic Testing Group. Genetic testing of children at risk for Huntington's disease. Neurology 1997; 49:1048-1053.
  9. Huntington's disease treatments. dnaMD-Genetic Conditions. http://www.dnamd.com/dnamd/content/conditions/treatmentdetailphys.asp?
    id=15&condition_name=Huntington%20Disease
    . 2000.