Electroclinical features of epilepsy in patients with juvenile type dentatorubral-pallidoluysian atrophy
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2008.01701.x/fullpdf
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2. A severe case of dentatorubro-pallidoluysian atrophy (DRPLA) with microcephaly, very early onset of seizures, and cerebral white matter involvement;Brunetti-Pierri;Neuropediatrics,2006
3. Epidemiological and medical aspects of epilepsy in the elderly;Cloyd;Epilepsy Res,2006
4. An unusual case of Larofa body disease;Corkill;Eur J Neurol,1999
5. ‘Baltic’ myoclonus epilepsy: hereditary disorder of childhood made worse by phenytoin;Elridge;Lancet,1983
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1. Establishing resources and increasing awareness to advance research on Dentatorubral-pallidoluysian atrophy toward a treatment: a patient organization perspective;Therapeutic Advances in Rare Disease;2024-01
2. Progressive Myoclonic Epilepsies;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05
3. Pathophysiological Analysis and Therapeutic Intervention of Dentatorubural-Pallidoluysian Atrophy (DRPLA) Transgenic Model Mice;Journal of the Japan Epilepsy Society;2020-06-30
4. Progressive Myoclonic Epilepsies;Handbook of the Cerebellum and Cerebellar Disorders;2020
5. Dentatorubral-pallidoluysian Atrophy: An Update;TREMOR OTHER HYPERK;2018
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