Hostname: page-component-848d4c4894-wzw2p Total loading time: 0 Render date: 2024-05-16T03:40:06.941Z Has data issue: false hasContentIssue false
  • English
  • Français

Summary and Concluding Remarks

Published online by Cambridge University Press:  05 January 2016

Donald B. Calne  and
Bruce S. Schoenberg
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
Other
Information
Canadian Journal of Neurological Sciences , Volume 14 , Issue S3 , August 1987 , pp. 555 - 556
Copyright
Copyright © Canadian Neurological Sciences Federation 1987

References

REFERENCES

1.Kurland, LT and Mulder, DW.Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregation indicative of dominant inheritance. Neurology 1955: 5: 182–96.CrossRefGoogle ScholarPubMed
2.Kurland, LT.Introductory remarks. Proceedings of the 3rd Conference on the toxicity of cycads. Fed Proc 1964: 23: 1337–1339.Google Scholar
3.Reed, D.Plato, C.Elizan, T, et al. The amyotrophic lateral sclerosis/parkinsonism-dementia complex: A ten-year follow-up on Guam. Am J of Epid 1966: 83, 1: 54–73.CrossRefGoogle Scholar
4.Whiting, MG.Toxicity of Cycads. Econ Bot 1963: 17: 271–302.CrossRefGoogle Scholar
5.Reed, DM, Brody, JA.Amyotrophic lateral sclerosis and parkinsonism-dementia on Guam. 1945–1972. I. Descriptive epidemiology. Am J of Epid 1975: 101. 4: 287–301.CrossRefGoogle Scholar
6.Garruto, RM.Yanagihara, R.Gajdusek, DC.Disappearance of highincidence amyotrophic lateral sclerosis and parkinsonism-dementia on Guam. Neurol 1985: 35: 193–198.CrossRefGoogle ScholarPubMed
7.Rodgers-Johnson, P, Garruto, RM, Yanagihara, R.et al. Amyotrophic lateral sclerosis and parkinsonism-dementia on Guam: A 30 yearold evaluation of clinical and neuropathologic trends. Neurol 1986; 36: 7–13.CrossRefGoogle Scholar
8.Spencer, PS.Schaumburg, HH.The pathogenesis of motor neuron disease: Perspectives from neurotoxicology. In: Human Motor Neuron Disease. Rowland, LP.Advances in Neurology, vol 36. Raven Press. N.Y.. 1982: 249.Google Scholar
9.Vega, A, Bell, EA.α-Amino-β-methylaminopropionic acid, a new amino acid from seeds of Cycas circinalis. Phytochemistry (Oxf) 1967; 6: 759–762.Google Scholar
10.Spencer, PS, Hugon, J, Ludolph, A.et al. Discovery and partial characterization of primate motor-system toxins. In: Bock, G.O’Connor, M. eds.. Selective Neuronal Death. Ciba Foundation Symposium, Wiley Interscience 1987: 221–238.Google Scholar
11.Richardson, JC, Steele, JC, Olszewski, J.Supranuclear opthalmoplegia pseudolbar palsy, nuchal dystonia and dementia: A clinical report on eight cases of “heterogeneous degeneration”. Trans Amer Neurol Assoc 1963; 88: 25–29.Google Scholar