A clinical and neurophysiological motor signature of Unverricht–Lundborg disease-Reference-Cited by-同舟云学术

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A clinical and neurophysiological motor signature of Unverricht–Lundborg disease

Published:2018-01 Issue:1-2 Volume:174 Page:56-65
ISSN:0035-3787
Container-title:Revue Neurologique
language:en
Short-container-title:Revue Neurologique

Author:

Hainque E.,Blancher A.,Mesnage V.,Rivaud-Pechoux S.,Bertrand A.,Dupont S.,Navarro V.,Roze E.,Gourfinkel-An I.,Apartis E.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference41 articles.

1. Progressive myoclonus epilepsies: clinical and genetic aspects;Berkovic;Epilepsia,1993

2. Classification of the myoclonic epilepsies;Leppik;Epilepsia,2003

3. Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2B;Chan;Adv Neurol,2005

4. Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects;Shahwan;Lancet Neurol,2005

5. The progressive myoclonic epilepsies;Malek;Pract Neurol,2015

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rethinking the neurophysiological concept of cortical myoclonus;Clinical Neurophysiology;2023-12

2. The Unverricht-Lundborg disease as a part of the progressive myoclonic epilepsies syndrome;Almanac of Clinical Medicine;2022-12-08

3. Juvenile myoclonic epilepsy phenotype in a family with Unverricht‐Lundborg disease;Epileptic Disorders;2019-08

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