MovDisordV3, Main, Exploration, bibRecord, 000571

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.

Identifieur interne : 000571 ( Main/Exploration ); précédent : 000570; suivant : 000572

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.

Auteurs : Lynn Rochester [Royaume-Uni] ; Brook Galna ; Sue Lord ; Dadirayi Mhiripiri ; Gail Eglon ; Patrick F. Chinnery

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.

RBID : pubmed:24301795

English descriptors

KwdEn :
- Adult, Aged, Calcium Channels (genetics), Disease Progression, Female, Gait Disorders, Neurologic (complications), Humans, Male, Middle Aged, Severity of Illness Index, Spinocerebellar Ataxias (complications), Spinocerebellar Ataxias (genetics).
MESH :
- chemical , genetics : Calcium Channels.
- complications : Gait Disorders, Neurologic, Spinocerebellar Ataxias.
- genetics : Spinocerebellar Ataxias.
- Adult, Aged, Disease Progression, Female, Humans, Male, Middle Aged, Severity of Illness Index.

Abstract

Spinocerebellar ataxia type 6 (SCA6) is an inherited ataxia with no established treatment. Gait ataxia is a prominent feature causing substantial disability. Understanding the evolution of the gait disturbance is a key step in developing treatment strategies.

DOI: 10.1002/mds.25706
PubMed: 24301795

Affiliations:

Royaume-Uni

Le document en format XML

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<author><name sortKey="Rochester, Lynn" sort="Rochester, Lynn" uniqKey="Rochester L" first="Lynn" last="Rochester">Lynn Rochester</name>
<affiliation wicri:level="1"><nlm:affiliation>Institute for Ageing and Health, Clinical Ageing Research Unit, Newcastle University, Newcastle upon Tyne, United Kingdom.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, Clinical Ageing Research Unit, Newcastle University, Newcastle upon Tyne</wicri:regionArea>
<wicri:noRegion>Newcastle upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Galna, Brook" sort="Galna, Brook" uniqKey="Galna B" first="Brook" last="Galna">Brook Galna</name>
</author>
<author><name sortKey="Lord, Sue" sort="Lord, Sue" uniqKey="Lord S" first="Sue" last="Lord">Sue Lord</name>
</author>
<author><name sortKey="Mhiripiri, Dadirayi" sort="Mhiripiri, Dadirayi" uniqKey="Mhiripiri D" first="Dadirayi" last="Mhiripiri">Dadirayi Mhiripiri</name>
</author>
<author><name sortKey="Eglon, Gail" sort="Eglon, Gail" uniqKey="Eglon G" first="Gail" last="Eglon">Gail Eglon</name>
</author>
<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F" last="Chinnery">Patrick F. Chinnery</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.</title>
<author><name sortKey="Rochester, Lynn" sort="Rochester, Lynn" uniqKey="Rochester L" first="Lynn" last="Rochester">Lynn Rochester</name>
<affiliation wicri:level="1"><nlm:affiliation>Institute for Ageing and Health, Clinical Ageing Research Unit, Newcastle University, Newcastle upon Tyne, United Kingdom.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, Clinical Ageing Research Unit, Newcastle University, Newcastle upon Tyne</wicri:regionArea>
<wicri:noRegion>Newcastle upon Tyne</wicri:noRegion>
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<author><name sortKey="Galna, Brook" sort="Galna, Brook" uniqKey="Galna B" first="Brook" last="Galna">Brook Galna</name>
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<author><name sortKey="Lord, Sue" sort="Lord, Sue" uniqKey="Lord S" first="Sue" last="Lord">Sue Lord</name>
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<author><name sortKey="Mhiripiri, Dadirayi" sort="Mhiripiri, Dadirayi" uniqKey="Mhiripiri D" first="Dadirayi" last="Mhiripiri">Dadirayi Mhiripiri</name>
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<author><name sortKey="Eglon, Gail" sort="Eglon, Gail" uniqKey="Eglon G" first="Gail" last="Eglon">Gail Eglon</name>
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<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F" last="Chinnery">Patrick F. Chinnery</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2014" type="published">2014</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Calcium Channels (genetics)</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Gait Disorders, Neurologic (complications)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Severity of Illness Index</term>
<term>Spinocerebellar Ataxias (complications)</term>
<term>Spinocerebellar Ataxias (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Calcium Channels</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Gait Disorders, Neurologic</term>
<term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Severity of Illness Index</term>
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<front><div type="abstract" xml:lang="en">Spinocerebellar ataxia type 6 (SCA6) is an inherited ataxia with no established treatment. Gait ataxia is a prominent feature causing substantial disability. Understanding the evolution of the gait disturbance is a key step in developing treatment strategies.</div>
</front>
</TEI>
<affiliations><list><country><li>Royaume-Uni</li>
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<tree><noCountry><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F" last="Chinnery">Patrick F. Chinnery</name>
<name sortKey="Eglon, Gail" sort="Eglon, Gail" uniqKey="Eglon G" first="Gail" last="Eglon">Gail Eglon</name>
<name sortKey="Galna, Brook" sort="Galna, Brook" uniqKey="Galna B" first="Brook" last="Galna">Brook Galna</name>
<name sortKey="Lord, Sue" sort="Lord, Sue" uniqKey="Lord S" first="Sue" last="Lord">Sue Lord</name>
<name sortKey="Mhiripiri, Dadirayi" sort="Mhiripiri, Dadirayi" uniqKey="Mhiripiri D" first="Dadirayi" last="Mhiripiri">Dadirayi Mhiripiri</name>
</noCountry>
<country name="Royaume-Uni"><noRegion><name sortKey="Rochester, Lynn" sort="Rochester, Lynn" uniqKey="Rochester L" first="Lynn" last="Rochester">Lynn Rochester</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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Movement Disorders (revue)

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.

Gait impairment precedes clinical symptoms in spinocerebellar ataxia type 6.

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

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

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.