Typical progression of myoclonic epilepsy of the Lafora type: a case report-Reference-Cited by-同舟云学术

Typical progression of myoclonic epilepsy of the Lafora type: a case report

Published:2008-02 Issue:2 Volume:4 Page:106-111
ISSN:1745-834X
Container-title:Nature Clinical Practice Neurology
language:en
Short-container-title:Nat Rev Neurol

Author:

Striano Pasquale,Zara Federico,Turnbull Julie,Girard Jean-Marie,Ackerley Cameron A,Cervasio Mariarosaria,De Rosa Gaetano,Del Basso-De Caro Maria Laura,Striano Salvatore,Minassian Berge A

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

Link

http://www.nature.com/articles/ncpneuro0706.pdf

Reference19 articles.

1. Lafora GR and Glueck B (1911) Contribution to the histopathology of the myoclonic epilepsies [German]. Z Gesamte Neurol Psychiatr 6: 1–14

2. Lohi H et al. (2006) On the road to tractability: the current biochemical understanding of progressive myoclonus epilepsies. Adv Neurol 97: 399–415

3. Boccella P et al. (2003) Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters. Clin Neurol Neurosurg 106: 55–59

4. Canafoglia L et al. (2004) Sensorimotor cortex excitability in Unverricht–Lundborg disease and Lafora body disease. Neurology 63: 2309–2315

5. Panzica F et al. (2003) Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG–EMG relationship estimated using autoregressive models. Clin Neurophysiol 114: 1041–1052

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