Seizures in juvenile Huntington's disease: Frequency and characterization in a multicenter cohort-Reference-Cited by-同舟云学术

Seizures in juvenile Huntington's disease: Frequency and characterization in a multicenter cohort

Published:2012-11-02 Issue:14 Volume:27 Page:1797-1800
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Cloud Leslie J.,Rosenblatt Adam,Margolis Russel L.,Ross Christopher A.,Pillai Jagan A.,Corey-Bloom Jody,Tully Hannah M.,Bird Thomas,Panegyres Peter K.,Nichter Charles A.,Higgins Donald S.,Helmers Sandra L.,Factor Stewart A.,Jones Randi,Testa Claudia M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25237/fullpdf

Reference10 articles.

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3. Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent;Telenius;Hum Mol Genet,1993

4. Factors influencing dementia and epilepsy in Huntington's disease of early onset;Brackenridge;Acta Neurol Scand,1980

5. EEG characteristics in juvenile Huntington's disease: a case report and review of the literature;Landau;Epileptic Disord,2003

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