Univerricht-Lundborg Disease: Underdiagnosed in the Netherlands-Reference-Cited by-同舟云学术

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Univerricht-Lundborg Disease: Underdiagnosed in the Netherlands

Published:2004-09 Issue:9 Volume:45 Page:1061-1063
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

de Haan Gerrit-Jan,Halley Dicky J.J.,Doelman Jan C.,Geesink Huibert H.,Augustijn Paul B.,Jager-Jongkind Anke D.,Majoie Marianne,Bader Adri J.,Doeschate Lian A.W.M. Leliefeld-ten,Deelen Wout H.,Bertram Ed,Lehesjoki Anna E.,Lindhout Dick

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0013-9580.2004.43703.x/fullpdf

Reference10 articles.

1. Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type

2. NEW EMBO MEMBER'S REVIEW: Molecular background of progressive myoclonus epilepsy

3. Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)

Cited by 26 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. The Roles of Cystatin B in the Brain and Pathophysiological Mechanisms of Progressive Myoclonic Epilepsy Type 1;Cells;2024-01-16

2. Negative myoclonus causes locomotory disability in progressive myoclonus epilepsy type EPM1‐ Unverricht‐Lundborg disease;Epileptic Disorders;2023-05-22

3. Clinical and molecular characterization of Unverricht–Lundborg disease among Egyptian patients;Epilepsy Research;2021-10

4. Prognosis;The Importance of Photosensitivity for Epilepsy;2020-12-24

5. Genetic testing and the phenotype of Polish patients with Unverricht–Lundborg disease (EPM1) — A cohort study;Epilepsy & Behavior;2020-11

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