White matter alterations in familial cortical myoclonic tremor with epilepsy type 1

Author:

Wang Bo1,Wang Haotian1,Cen Zhidong1,Yuan Jiachen1,Yang Dehao1,Chen Xinhui1,Xie Fei2,Wang Lebo1,Wu Sheng1,Ouyang Zhiyuan1,Zang Yu‐Feng34,Luo Wei1ORCID

Affiliation:

1. Department of Neurology Second Affiliated Hospital Zhejiang University School of Medicine Hangzhou China

2. Department of Neurology Sir Run Run Shaw Hospital Zhejiang University School of Medicine Hangzhou China

3. Center for Cognition and Brain Disorders Institute of Psychological Sciences Hangzhou Normal University Hangzhou China

4. Zhejiang Key Laboratory for Research in Assessment of Cognitive Impairments Hangzhou China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference35 articles.

1. Familial cortical myoclonic tremor and epilepsy, an enigmatic disorder: from phenotypes to pathophysiology and genetics. A systematic review;Ende T;Tremor Other Hyperkinet Mov,2018

2. Nationwide survey in Japan endorsed diagnostic criteria of benign adult familial myoclonus epilepsy

3. Electroencephalographic features of benign adult familial myoclonic epilepsy

4. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy

5. Familial cortical myoclonic tremor with epilepsy and cerebellar changes: description of a new pathology case and review of the literature;Sharifi S;Tremor Other Hyperkinet Mov,2012

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