Short‐ and long‐interval intracortical inhibition in <scp>EPM1</scp> is related to genotype-Reference-Cited by-同舟云学术

Short‐ and long‐interval intracortical inhibition in EPM1 is related to genotype

Published:2022-12 Issue:1 Volume:64 Page:208-217
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Silvennoinen Katri¹²³^ORCID,Säisänen Laura⁴⁵,Hyppönen Jelena⁴,Rissanen Saara M.⁵,Karjalainen Pasi A.⁵,D'Ambrosio Sasha²⁶^ORCID,Jimenez‐Jimenez Diego²,Zagaglia Sara²,Rothwell John C.⁷,Balestrini Simona²³⁸^ORCID,Sisodiya Sanjay M.²³^ORCID,Julkunen Petro⁴⁵^ORCID,Mervaala Esa⁴⁹,Kälviäinen Reetta¹⁹^ORCID

Affiliation:

1. Kuopio Epilepsy Center, Neurocenter Member of ERN EpiCARE, Kuopio University Hospital Kuopio Finland

2. Department of Clinical and Experimental Epilepsy UCL Queen Square Institute of Neurology London UK

3. Chalfont Centre for Epilepsy UK

4. Department of Clinical Neurophysiology, Kuopio Epilepsy Center, Neurocenter Member of ERN EpiCARE, Kuopio University Hospital Kuopio Finland

5. Department of Applied Physics University of Eastern Finland Kuopio Finland

6. Dipartimento di Scienze Biomediche e Cliniche "L. Sacco" Università degli Studi di Milano Milan Italy

7. Sobell Department of Motor Neuroscience and Movement Disorders UCL Queen Square Institute of Neurology London UK

8. Neuroscience Department Member of ERN EpiCARE, Meyer Children Hospital Florence Italy

9. Institute of Clinical Medicine, School of Medicine, Faculty of Health Sciences University of Eastern Finland Kuopio Finland

Funder

Business Finland

University of Kentucky

Muir Maxwell Trust

National Brain Appeal

Academy of Finland

UCB UK

University College London Hospitals Biomedical Research Centre

Wellcome Trust

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.17466

Reference31 articles.

1. Clinical picture of EPM1-Unverricht-Lundborg disease

2. Refining the phenotype of Unverricht-Lundborg disease (EPM1): A population-wide Finnish study

3. Molecular background of EPM1—Unverricht–Lundborg disease

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

5. Cystatin B is essential for proliferation and interneuron migration in individuals with EPM 1 epilepsy

Cited by 7 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. Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic Advances;Genes;2024-01-27

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

3. In depth behavioral phenotyping unravels complex motor disturbances in Cstb−/− mouse, a model for progressive myoclonus epilepsy type 1;Frontiers in Behavioral Neuroscience;2023-12-21

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

5. Detecting negative myoclonus during long-term home measurements using wearables;Clinical Neurophysiology;2023-12