Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation-Reference-Cited by-同舟云学术

Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation

Published:2013-10-30 Issue:1 Volume:29 Page:139-143
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

van Egmond Martje E.¹,Verschuuren-Bemelmans Corien C.²,Nibbeling Esther A.²,Elting Jan Willem J.¹,Sival Deborah A.³,Brouwer Oebele F.¹,de Vries Jeroen J.¹,Kremer Hubertus P.¹,Sinke Richard J.²,Tijssen Marina A.¹,de Koning Tom J.¹²

Affiliation:

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

2. Department of Genetics; University of Groningen, University Medical Center Groningen; The Netherlands

3. Department of Pediatrics; University of Groningen, University Medical Center Groningen; The Netherlands

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25704/fullpdf

Reference8 articles.

1. Dyssynergia cerebellaris myoclonica-primary atrophy of the dentate system: a contribution to the pathology and symptomatology of the cerebellum;Ramsay Hunt;Brain,1921

2. Recent advances in hereditary spinocerebellar ataxias;Warrenburg;J Neuropathol Exp Neurol,2005

3. Progressive myoclonic ataxia (the Ramsay Hunt syndrome);Marsden;Arch Neurol,1990

4. PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype;Visser;Mov Disord,2007

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