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Clinical Problems of Motor System Disease

Published online by Cambridge University Press:  18 September 2015

J.C. Richardson*
Affiliation:
Section of neurology, Toronto General Hospital
*
Ste. 305-170 St. George Street, Toronto, Ontario M5R 2M8
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Summary:

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This prologue to a symposium of research studies on motor mechanisms is a general commentary by a clinical neurologist. The vast extent and intricacy of modern basic neurological scientific knowledge presents a rather bewildering challenge to reasonable clinical application. In some degree this is being handled by complex and diverse neurological subspecialization. It is recalled that many past advances in the knowledge of neurological disease were achieved by a series of alternating and supporting bedside and laboratory observations and studies.

The varied disorders of movement and muscle tone which signal disordered motor mechanisms will continue to demand explanation and will keep the human model in a leading research position. Clinical and laboratory research leading to part discoveries of mechanisms of disease is sometimes productive of dramatic new means of therapy. The story of Wilson’s disease is briefly reviewed in that context. Some recent studies on hypoxic myoclonus are described with the evidence of a serotonin defect and useful related therapy.

Type
Research Article
Copyright
Copyright © Canadian Neurological Sciences Federation 1975

References

REFERENCES

Aring, Charles D. (1965). A tribute to Sir Gordon Holmes. Journal of Nervous and Mental Disease, 5, 497502.CrossRefGoogle Scholar
Castaigne, P., Cambier, J., Escourolle, R., Cathala, H.P. et Lecasble, R. (1964). Observation anatomo-clinique d’un syndrome myoclonique post-anoxique. Revue Neurologique 3, I,6073.Google Scholar
Denny-Brown, Derek (1965). A tribute to Sir Gordon Holmes. Journal of Nervous and Mental Disease, 5, 502504.CrossRefGoogle Scholar
Holmes, Gordon (1939). The Cerebellum of Man. Brain, 62, 130.CrossRefGoogle Scholar
Lance, James W. and Adams, Raymond D. (1963). The Syndrome of Intention or Action Myoclonus as a Sequel to Hypoxic Encephalopathy. Brain, 86, 111136.CrossRefGoogle ScholarPubMed
Lhermitte, F., Peterfalvi, M., Marteau, R., Gazengel, J. et Serdaru, M. (1971). Analyse pharmacologique d’un cas de myoclonies d’intention et d’actioh postanoxiques. Revue Neurologique Paris, 124, 2131.Google Scholar
Mandelbrote, B.M., Stanier, M., Thompson, R.H.S., Thruston, M.N. (1948). Studies on copper metabolism in demyelinating diseases of central nervous system. Brain, 71, 212228.CrossRefGoogle ScholarPubMed
Sternlieb, I., Van Den Horner, C.J.A., Morell, A.G., Alpert, S., Gregoriades, G. and Scheinberg, I.H. (1973). Lysosomal Defect of Copper Excretion in Wilson’s Disease (Hepatolenticular Degeneration). Gastroenterology, 64, 1, 99105.CrossRefGoogle ScholarPubMed
Walshe, F.M.R. (1956). Preface. Selected Papers of Sir Gordon Holmes.7–9. MacMillan & Co. Ltd., New York.Google Scholar