Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force-Reference-Cited by-同舟云学术

Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force

Published:2019-10-04 Issue:11 Volume:34 Page:1602-1613
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Veen Sterre¹,Zutt Rodi¹²,Klein Christine³,Marras Connie⁴,Berkovic Samuel F.⁵,Caviness John N.⁶,Shibasaki Hiroshi⁷,Koning Tom J.¹⁸,Tijssen Marina A.J.¹^ORCID

Affiliation:

1. Department of Neurology University Groningen, University Medical Center Groningen Groningen Netherlands

2. Department of Neurology Haga Teaching Hospital The Hague The Netherlands

3. Institute of Neurogenetics University of Lübeck Lübeck Germany

4. Edmond J. Safra Program in Parkinson's Disease Toronto Western Hospital, University of Toronto Toronto Ontario Canada

5. Epilepsy Research Center, Department of Medicine University of Melbourne, Austin Health Heidelberg Victoria Australia

6. Department of Neurology Mayo Clinic Scottsdale Arizona USA

7. Kyoto University Graduate School of Medicine Kyoto Japan

8. Department of Genetics University of Groningen, University Medical Centre Groningen Groningen The Netherlands

Funder

International Parkinson and Movement Disorder Society

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27828

Reference110 articles.

1. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

2. The genetic nomenclature of recessive cerebellar ataxias

3. Myoclonus.

4. The Neurologic Examination

5. Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment

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