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55 - Progressive Myoclonic Ataxia and Coeliac Disease

from Section 6 - Myoclonus

Published online by Cambridge University Press:  04 July 2017

Kailash P. Bhatia ,
Roberto Erro  and
Maria Stamelou
By
Roberto Erro  and
Kailash P. Bhatia
Kailash P. Bhatia
Affiliation:
Institute of Neurology, University College London
Roberto Erro
Affiliation:
Università degli Studi di Salerno, Italy
Maria Stamelou
Affiliation:
University of Athens, Greece
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Case Studies in Movement Disorders
Common and Uncommon Presentations
 , pp. 123 - 124
Publisher: Cambridge University Press
Print publication year: 2017

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References

Suggested Readings

Bhatia, KP, Brown, P, Gregory, R, et al. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain. 1995;118:1087–93.CrossRefGoogle ScholarPubMed
Ganos, C, Kassavetis, P, Erro, R, Edwards, MJ, Rothwell, J, Bhatia, KP. The role of the cerebellum in the pathogenesis of cortical myoclonus. Mov Disord. 2014;29:437–43.CrossRefGoogle ScholarPubMed
Lu, CS, Thompson, PD, Quinn, NP, Parkes, JD, Marsden, CD. Ramsay Hunt syndrome and coeliac disease: a new association? Mov Disord. 1986;1:209–19.CrossRefGoogle ScholarPubMed

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