MovDisordV3, Main, Exploration, bibRecord, 002194

Myoclonus‐dystonia: An update

Identifieur interne : 002194 ( Main/Exploration ); précédent : 002193; suivant : 002195

Myoclonus‐dystonia: An update

Auteurs : Kiyoka Kinugawa [France] ; Marie Vidailhet [France] ; Fabienne Clot [France] ; Emmanuelle Apartis [France] ; David Grabli [France] ; Emmanuel Roze [France]

Source :

Movement Disorders [ 0885-3185 ] ; 2009-03-15.

RBID : ISTEX:25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3

Descripteurs français

Pascal (Inist)
- Dystonie, Myoclonie, Neurologie, Pathologie du système nerveux, Physiopathologie.
Wicri :
- topic : Neurologie.

English descriptors

KwdEn :
- Diagnosis, Differential, Dystonia, Dystonia (complications), Dystonia (diagnosis), Dystonia (genetics), Dystonia (therapy), Humans, Magnetic Resonance Imaging (methods), Movement Disorders (genetics), Movement Disorders (physiopathology), Movement Disorders (therapy), Mutation (genetics), Myoclonus, Myoclonus (complications), Myoclonus (diagnosis), Myoclonus (genetics), Myoclonus (therapy), Nervous system diseases, Neurology, Pathophysiology, Sarcoglycans (genetics), clinical neurology, epsilon‐sarcoglycan, genetics, myoclonus‐dystonia, pathophysiology, primary dystonia.
MESH :
- chemical , genetics : Sarcoglycans.
- complications : Dystonia, Myoclonus.
- diagnosis : Dystonia, Myoclonus.
- genetics : Dystonia, Movement Disorders, Mutation, Myoclonus.
- methods : Magnetic Resonance Imaging.
- physiopathology : Movement Disorders.
- therapy : Dystonia, Movement Disorders, Myoclonus.
- Diagnosis, Differential, Humans.

Abstract

Our knowledge of the clinical, neurophysiological, and genetic aspects of myoclonus‐dystonia (M‐D) has improved markedly in the recent years. Basic research has provided new insights into the complex dysfunctions involved in the pathogenesis of M‐D. On the basis of a comprehensive literature search, this review summarizes current knowledge on M‐D, with a focus on recent findings. We also propose modified diagnostic criteria and recommendationsfor clinical management. © 2008 Movement Disorder Society

Url:

https://api.istex.fr/document/25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3/fulltext/pdf

DOI: 10.1002/mds.22425

Affiliations:

France
Paris

Le document en format XML

<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Myoclonus‐dystonia: An update</title>
<author><name sortKey="Kinugawa, Kiyoka" sort="Kinugawa, Kiyoka" uniqKey="Kinugawa K" first="Kiyoka" last="Kinugawa">Kiyoka Kinugawa</name>
</author>
<author><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
</author>
<author><name sortKey="Clot, Fabienne" sort="Clot, Fabienne" uniqKey="Clot F" first="Fabienne" last="Clot">Fabienne Clot</name>
</author>
<author><name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name>
</author>
<author><name sortKey="Grabli, David" sort="Grabli, David" uniqKey="Grabli D" first="David" last="Grabli">David Grabli</name>
</author>
<author><name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3</idno>
<date when="2009" year="2009">2009</date>
<idno type="doi">10.1002/mds.22425</idno>
<idno type="url">https://api.istex.fr/document/25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001984</idno>
<idno type="wicri:Area/Istex/Curation">001984</idno>
<idno type="wicri:Area/Istex/Checkpoint">000D96</idno>
<idno type="wicri:doubleKey">0885-3185:2009:Kinugawa K:myoclonus:dystonia:an</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:19117361</idno>
<idno type="wicri:Area/PubMed/Corpus">001E86</idno>
<idno type="wicri:Area/PubMed/Curation">001E86</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001D01</idno>
<idno type="wicri:Area/Ncbi/Merge">002478</idno>
<idno type="wicri:Area/Ncbi/Curation">002478</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002478</idno>
<idno type="wicri:Area/Main/Merge">002A55</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:09-0171583</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000F45</idno>
<idno type="wicri:Area/PascalFrancis/Curation">001D74</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000D95</idno>
<idno type="wicri:doubleKey">0885-3185:2009:Kinugawa K:myoclonus:dystonia:an</idno>
<idno type="wicri:Area/Main/Merge">002E92</idno>
<idno type="wicri:Area/Main/Curation">002194</idno>
<idno type="wicri:Area/Main/Exploration">002194</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Myoclonus‐dystonia: An update</title>
<author><name sortKey="Kinugawa, Kiyoka" sort="Kinugawa, Kiyoka" uniqKey="Kinugawa K" first="Kiyoka" last="Kinugawa">Kiyoka Kinugawa</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>INSERM U679, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>University Paris 6‐Pierre et Marie Curie, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>INSERM U679, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>University Paris 6‐Pierre et Marie Curie, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Department of Neurology, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Clot, Fabienne" sort="Clot, Fabienne" uniqKey="Clot F" first="Fabienne" last="Clot">Fabienne Clot</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Department of Genetics and Cytogenetics, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>University Paris 6‐Pierre et Marie Curie, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Department of Physiology, Saint‐Antoine Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Grabli, David" sort="Grabli, David" uniqKey="Grabli D" first="David" last="Grabli">David Grabli</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>INSERM U679, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>University Paris 6‐Pierre et Marie Curie, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Department of Neurology, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>University Paris 6‐Pierre et Marie Curie, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>Department of Neurology, Pitié‐Salpêtrière Hospital, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">France</country>
<wicri:regionArea>CNRS UMR 7102, Paris</wicri:regionArea>
<placeName><settlement type="city">Paris</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2009-03-15">2009-03-15</date>
<biblScope unit="vol">24</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="479">479</biblScope>
<biblScope unit="page" to="489">489</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3</idno>
<idno type="DOI">10.1002/mds.22425</idno>
<idno type="ArticleID">MDS22425</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Dystonia</term>
<term>Dystonia (complications)</term>
<term>Dystonia (diagnosis)</term>
<term>Dystonia (genetics)</term>
<term>Dystonia (therapy)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging (methods)</term>
<term>Movement Disorders (genetics)</term>
<term>Movement Disorders (physiopathology)</term>
<term>Movement Disorders (therapy)</term>
<term>Mutation (genetics)</term>
<term>Myoclonus</term>
<term>Myoclonus (complications)</term>
<term>Myoclonus (diagnosis)</term>
<term>Myoclonus (genetics)</term>
<term>Myoclonus (therapy)</term>
<term>Nervous system diseases</term>
<term>Neurology</term>
<term>Pathophysiology</term>
<term>Sarcoglycans (genetics)</term>
<term>clinical neurology</term>
<term>epsilon‐sarcoglycan</term>
<term>genetics</term>
<term>myoclonus‐dystonia</term>
<term>pathophysiology</term>
<term>primary dystonia</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Sarcoglycans</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Dystonia</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Dystonia</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonia</term>
<term>Movement Disorders</term>
<term>Mutation</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Magnetic Resonance Imaging</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Movement Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Dystonia</term>
<term>Movement Disorders</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dystonie</term>
<term>Myoclonie</term>
<term>Neurologie</term>
<term>Pathologie du   système nerveux</term>
<term>Physiopathologie</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Neurologie</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Our knowledge of the clinical, neurophysiological, and genetic aspects of myoclonus‐dystonia (M‐D) has improved markedly in the recent years. Basic research has provided new insights into the complex dysfunctions involved in the pathogenesis of M‐D. On the basis of a comprehensive literature search, this review summarizes current knowledge on M‐D, with a focus on recent findings. We also propose modified diagnostic criteria and recommendationsfor clinical management. © 2008 Movement Disorder Society</div>
</front>
</TEI>
<affiliations><list><country><li>France</li>
</country>
<settlement><li>Paris</li>
</settlement>
</list>
<tree><country name="France"><noRegion><name sortKey="Kinugawa, Kiyoka" sort="Kinugawa, Kiyoka" uniqKey="Kinugawa K" first="Kiyoka" last="Kinugawa">Kiyoka Kinugawa</name>
</noRegion>
<name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name>
<name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name>
<name sortKey="Clot, Fabienne" sort="Clot, Fabienne" uniqKey="Clot F" first="Fabienne" last="Clot">Fabienne Clot</name>
<name sortKey="Grabli, David" sort="Grabli, David" uniqKey="Grabli D" first="David" last="Grabli">David Grabli</name>
<name sortKey="Grabli, David" sort="Grabli, David" uniqKey="Grabli D" first="David" last="Grabli">David Grabli</name>
<name sortKey="Grabli, David" sort="Grabli, David" uniqKey="Grabli D" first="David" last="Grabli">David Grabli</name>
<name sortKey="Kinugawa, Kiyoka" sort="Kinugawa, Kiyoka" uniqKey="Kinugawa K" first="Kiyoka" last="Kinugawa">Kiyoka Kinugawa</name>
<name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
<name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
<name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
<name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
<name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
<name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002194 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002194 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:25FC68EE5B2EA1207E550F435CA1EAEB75FA6FF3
   |texte=   Myoclonus‐dystonia: An update
}}

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024

Movement Disorders (revue)

Myoclonus‐dystonia: An update

Myoclonus‐dystonia: An update

Source :

Descripteurs français

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

	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.