Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction-Reference-Cited by-同舟云学术

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Twenty years on: Myoclonus‐dystonia and ε‐sarcoglycan — neurodevelopment, channel, and signaling dysfunction

Published:2019-08-26 Issue:11 Volume:34 Page:1588-1601
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Menozzi Elisa¹²,Balint Bettina²³,Latorre Anna²⁴^ORCID,Valente Enza Maria⁵⁶,Rothwell John C.²^ORCID,Bhatia Kailash P.²^ORCID

Affiliation:

1. Department of Biomedical, Metabolic and Neural Sciences University‐Hospital of Modena and Reggio Emilia Modena Italy

2. Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology London UK

3. Department of Neurology University Hospital Heidelberg Heidelberg Germany

4. Department of Human Neurosciences Sapienza University of Rome Rome Italy

5. Department of Molecular Medicine University of Pavia Pavia Italy

6. Neurogenetics Unit IRCCS Santa Lucia Foundation Rome Italy

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27822

Reference203 articles.

1. Myoclonic dystonia

2. Inherited myoclonus‐dystonia syndrome;Gasser T.;Adv Neurol,1998

3. Essential myoclonus and myoclonus dystonia

4. Dystonia-plus syndromes

5. Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families

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1. Deciphering the Pathophysiological Mechanisms Underpinning Myoclonus Dystonia Using Pluripotent Stem Cell-Derived Cellular Models;Cells;2024-09-10

2. Novel SGCE Mutation in a Patient With Myoclonus-Dystonia;Neurology Genetics;2024-04

3. ε-sarcoglycan myoclonus-dystonia—overview of neurophysiological, behavioral, and imaging characteristics;Dystonia;2024-02-21

4. Myoclonus: Differential diagnosis and current management;Epilepsia Open;2024-02-09

5. Genetics and Pathogenesis of Dystonia;Annual Review of Pathology: Mechanisms of Disease;2024-01-24

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