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58 - Familial Cortical ‘Tremor’

from Section 6 - Myoclonus

Published online by Cambridge University Press:  04 July 2017

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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Summary

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Chapter
Information
Case Studies in Movement Disorders
Common and Uncommon Presentations
, pp. 129 - 130
Publisher: Cambridge University Press
Print publication year: 2017

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References

Suggested Readings

Cen, Z, Huang, C, Yin, H, et al. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy. Mov Disord. 2016;31:17041710.Google Scholar
Gao, L, Li, L, Ye, J, et al. Identification of a novel mutation in PLA2G6 gene in a Chinese pedigree with familial cortical myoclonic tremor with epilepsy. Seizure. 2016;41:81–5.CrossRefGoogle Scholar
Martí-Massó, JF, Bergareche, A, Makarov, V, et al. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. J Mol Med (Berl). 2013;91:1399–406.CrossRefGoogle Scholar
Stogmann, E, Reinthaler, E, Eltawil, S, et al. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain. 2013;136:1155–60.Google Scholar
van Rootselaar, AF, van Schaik, IN, van den Maagdenberg, AM, et al. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov Disord. 2005;20:665–73.Google Scholar

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