Alterations of motor cortical excitability and anatomy in Unverricht-Lundborg disease-Reference-Cited by-同舟云学术

Alterations of motor cortical excitability and anatomy in Unverricht-Lundborg disease

Published:2013-08-07 Issue:13 Volume:28 Page:1860-1867
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Danner Nils¹²,Julkunen Petro²,Hyppönen Jelena²,Niskanen Eini³⁴,Säisänen Laura¹²,Könönen Mervi²³,Koskenkorva Päivi³,Vanninen Ritva¹³,Kälviäinen Reetta¹⁵,Mervaala Esa¹²

Affiliation:

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

2. Department of Clinical Neurophysiology; Kuopio University Hospital; Kuopio Finland

3. Department of Clinical Radiology; Kuopio University Hospital; Kuopio Finland

4. Department of Applied Physics; University of Eastern Finland; Kuopio Finland

5. Department of Neurology; Kuopio University Hospital; Kuopio Finland

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25615/fullpdf

Reference59 articles.

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

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

3. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy;Lalioti;Nature.,1997

4. Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1;Virtaneva;Nat Genet.,1997

5. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1);Pennacchio;Science.,1996

Cited by 19 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. Detecting negative myoclonus during long-term home measurements using wearables;Clinical Neurophysiology;2023-12

2. Progressive myoclonic epilepsy type 1 (EPM1) patients present with abnormal 1H MRS brain metabolic profiles associated with cognitive function;NeuroImage: Clinical;2023

3. Short‐ and long‐interval intracortical inhibition in EPM1 is related to genotype;Epilepsia;2022-12

4. Cognitive functioning in progressive myoclonus epilepsy type 1 (Unverricht-Lundborg Disease, EPM1);Epilepsy & Behavior;2021-09

5. Transcranial magnetic stimulation as a tool to understand genetic conditions associated with epilepsy;Epilepsia;2020-08-12