MovDisordV3, Main, Exploration, bibRecord, 001137

Dystonia in Mitochondrial Spinocerebellar Ataxia and Epilepsy Syndrome Associated with Novel Recessive POLG Mutations

Identifieur interne : 001137 ( Main/Exploration ); précédent : 001136; suivant : 001138

Dystonia in Mitochondrial Spinocerebellar Ataxia and Epilepsy Syndrome Associated with Novel Recessive POLG Mutations

Auteurs : Claire Hinnell [Royaume-Uni] ; Salman Haider [Royaume-Uni] ; Shane Delamont [Royaume-Uni] ; Chris Clough [Royaume-Uni] ; Nedim Hadzic [Royaume-Uni] ; Michael Samuel [Royaume-Uni]

Source :

Movement disorders [ 0885-3185 ] ; 2012.

RBID : Pascal:12-0106528

Descripteurs français

Pascal (Inist)
- Dystonie, Epilepsie, Pathologie du système nerveux, Mitochondrie, Ataxie spinocérébelleuse, Mutation.

English descriptors

KwdEn :
- Dystonia, Epilepsy, Mitochondria, Mutation, Nervous system diseases, Spinocerebellar ataxia.

Affiliations:

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

to stream PascalFrancis, to step Corpus: 000287
to stream PascalFrancis, to step Curation: 002A27
to stream PascalFrancis, to step Checkpoint: 000210
to stream Main, to step Merge: 001189
to stream Main, to step Curation: 001137

Le document en format XML

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<author><name sortKey="Hinnell, Claire" sort="Hinnell, Claire" uniqKey="Hinnell C" first="Claire" last="Hinnell">Claire Hinnell</name>
<affiliation wicri:level="3"><inist:fA14 i1="01"><s1>King's College Hospital, Department of Neurology</s1>
<s2>London</s2>
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<country>Royaume-Uni</country>
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<author><name sortKey="Hadzic, Nedim" sort="Hadzic, Nedim" uniqKey="Hadzic N" first="Nedim" last="Hadzic">Nedim Hadzic</name>
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<author><name sortKey="Samuel, Michael" sort="Samuel, Michael" uniqKey="Samuel M" first="Michael" last="Samuel">Michael Samuel</name>
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<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>East Kent Hospitals NHS University Trust, William Harvey Hospital</s1>
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<country>Royaume-Uni</country>
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<author><name sortKey="Haider, Salman" sort="Haider, Salman" uniqKey="Haider S" first="Salman" last="Haider">Salman Haider</name>
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<author><name sortKey="Delamont, Shane" sort="Delamont, Shane" uniqKey="Delamont S" first="Shane" last="Delamont">Shane Delamont</name>
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<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
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<author><name sortKey="Samuel, Michael" sort="Samuel, Michael" uniqKey="Samuel M" first="Michael" last="Samuel">Michael Samuel</name>
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<region type="country">Angleterre</region>
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<country>Royaume-Uni</country>
<wicri:noRegion>Ashford</wicri:noRegion>
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<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
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<seriesStmt><title level="j" type="main">Movement disorders</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dystonia</term>
<term>Epilepsy</term>
<term>Mitochondria</term>
<term>Mutation</term>
<term>Nervous system diseases</term>
<term>Spinocerebellar ataxia</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dystonie</term>
<term>Epilepsie</term>
<term>Pathologie du   système nerveux</term>
<term>Mitochondrie</term>
<term>Ataxie spinocérébelleuse</term>
<term>Mutation</term>
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<tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Hinnell, Claire" sort="Hinnell, Claire" uniqKey="Hinnell C" first="Claire" last="Hinnell">Claire Hinnell</name>
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<name sortKey="Clough, Chris" sort="Clough, Chris" uniqKey="Clough C" first="Chris" last="Clough">Chris Clough</name>
<name sortKey="Delamont, Shane" sort="Delamont, Shane" uniqKey="Delamont S" first="Shane" last="Delamont">Shane Delamont</name>
<name sortKey="Hadzic, Nedim" sort="Hadzic, Nedim" uniqKey="Hadzic N" first="Nedim" last="Hadzic">Nedim Hadzic</name>
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<name sortKey="Samuel, Michael" sort="Samuel, Michael" uniqKey="Samuel M" first="Michael" last="Samuel">Michael Samuel</name>
<name sortKey="Samuel, Michael" sort="Samuel, Michael" uniqKey="Samuel M" first="Michael" last="Samuel">Michael Samuel</name>
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</record>

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	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.

Movement Disorders (revue)

Dystonia in Mitochondrial Spinocerebellar Ataxia and Epilepsy Syndrome Associated with Novel Recessive POLG Mutations

Dystonia in Mitochondrial Spinocerebellar Ataxia and Epilepsy Syndrome Associated with Novel Recessive POLG Mutations

Source :

Descripteurs français

English descriptors

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