MovDisordV3, PubMed, Corpus, bibRecord, 000B21

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Identifieur interne : 000B21 ( PubMed/Corpus ); précédent : 000B20; suivant : 000B22

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Auteurs : Mwiza Ushe ; Joel S. Perlmutter

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.

RBID : pubmed:23283653

English descriptors

KwdEn :
- Atrophy, Dystonia (diagnosis), Dystonia (etiology), Dystonia (genetics), Female, Genetic Predisposition to Disease (genetics), Humans, Middle Aged, Spinocerebellar Degenerations (complications), Spinocerebellar Degenerations (genetics).
MESH :
- complications : Spinocerebellar Degenerations.
- diagnosis : Dystonia.
- etiology : Dystonia.
- genetics : Dystonia, Genetic Predisposition to Disease, Spinocerebellar Degenerations.
- Atrophy, Female, Humans, Middle Aged.

DOI: 10.1002/mds.25295
PubMed: 23283653

Links to Exploration step

pubmed:23283653

Le document en format XML

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<author><name sortKey="Ushe, Mwiza" sort="Ushe, Mwiza" uniqKey="Ushe M" first="Mwiza" last="Ushe">Mwiza Ushe</name>
<affiliation><nlm:affiliation>Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.</nlm:affiliation>
</affiliation>
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<author><name sortKey="Perlmutter, Joel S" sort="Perlmutter, Joel S" uniqKey="Perlmutter J" first="Joel S" last="Perlmutter">Joel S. Perlmutter</name>
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<term>Female</term>
<term>Genetic Predisposition to Disease (genetics)</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Spinocerebellar Degenerations (complications)</term>
<term>Spinocerebellar Degenerations (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Spinocerebellar Degenerations</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Dystonia</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonia</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonia</term>
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<term>Spinocerebellar Degenerations</term>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Handb Clin Neurol. 2011;100:481-511</RefSource>
<PMID Version="1">21496604</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neuropsychol Rev. 2010 Sep;20(3):261-70</RefSource>
<PMID Version="1">20811947</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Parkinsonism Relat Disord. 2010 May;16(4):288-9</RefSource>
<PMID Version="1">19913450</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neurology. 2006 Nov 28;67(10):1769-73</RefSource>
<PMID Version="1">17130408</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Handb Clin Neurol. 2012;103:493-505</RefSource>
<PMID Version="1">21827909</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):459-65</RefSource>
<PMID Version="1">14966165</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Cerebellum. 2005;4(1):2-6</RefSource>
<PMID Version="1">15895552</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neuroimage. 2012 Oct 1;62(4):2261-70</RefSource>
<PMID Version="1">22206967</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neurology. 2006 Oct 24;67(8):1479-81</RefSource>
<PMID Version="1">17060579</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Mov Disord. 2006 Mar;21(3):293-8</RefSource>
<PMID Version="1">16211610</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="CommentIn"><RefSource>Mov Disord. 2012 Dec;27(14):1743</RefSource>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001284">Atrophy</DescriptorName>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Source :

English descriptors

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki