MovDisordV3, Main, Exploration, bibRecord, 001737

Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family

Identifieur interne : 001737 ( Main/Exploration ); précédent : 001736; suivant : 001738

Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family

Auteurs : Birgit Zirn [Allemagne] ; Christoph Korenke [Allemagne] ; Michael Wagner [Allemagne] ; Sabine Rudnik-Schöneborn [Allemagne] ; Ulrich Müller [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2011-02-01.

RBID : ISTEX:6FCCD7EB8652F36E37F141DB44C65E8201E45F9E

English descriptors

KwdEn :
- Adolescent, Adult, Charcot-Marie-Tooth Disease (complications), Charcot-Marie-Tooth Disease (genetics), Dystonic Disorders (complications), Dystonic Disorders (genetics), Female, Humans, Male.
MESH :
- complications : Charcot-Marie-Tooth Disease, Dystonic Disorders.
- genetics : Charcot-Marie-Tooth Disease, Dystonic Disorders.
- Adolescent, Adult, Female, Humans, Male.

Url:

https://api.istex.fr/document/6FCCD7EB8652F36E37F141DB44C65E8201E45F9E/fulltext/pdf

DOI: 10.1002/mds.23437

Affiliations:

Le document en format XML

<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family</title>
<author><name sortKey="Zirn, Birgit" sort="Zirn, Birgit" uniqKey="Zirn B" first="Birgit" last="Zirn">Birgit Zirn</name>
</author>
<author><name sortKey="Korenke, Christoph" sort="Korenke, Christoph" uniqKey="Korenke C" first="Christoph" last="Korenke">Christoph Korenke</name>
</author>
<author><name sortKey="Wagner, Michael" sort="Wagner, Michael" uniqKey="Wagner M" first="Michael" last="Wagner">Michael Wagner</name>
</author>
<author><name sortKey="Rudnik Choneborn, Sabine" sort="Rudnik Choneborn, Sabine" uniqKey="Rudnik Choneborn S" first="Sabine" last="Rudnik-Schöneborn">Sabine Rudnik-Schöneborn</name>
</author>
<author><name sortKey="Muller, Ulrich" sort="Muller, Ulrich" uniqKey="Muller U" first="Ulrich" last="Müller">Ulrich Müller</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:6FCCD7EB8652F36E37F141DB44C65E8201E45F9E</idno>
<date when="2011" year="2011">2011</date>
<idno type="doi">10.1002/mds.23437</idno>
<idno type="url">https://api.istex.fr/document/6FCCD7EB8652F36E37F141DB44C65E8201E45F9E/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002619</idno>
<idno type="wicri:Area/Istex/Curation">002619</idno>
<idno type="wicri:Area/Istex/Checkpoint">000470</idno>
<idno type="wicri:doubleKey">0885-3185:2011:Zirn B:concurrence:of:dystonia</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:21412843</idno>
<idno type="wicri:Area/PubMed/Corpus">001382</idno>
<idno type="wicri:Area/PubMed/Curation">001382</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001407</idno>
<idno type="wicri:Area/Ncbi/Merge">003042</idno>
<idno type="wicri:Area/Ncbi/Curation">003042</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">003042</idno>
<idno type="wicri:Area/Main/Merge">001791</idno>
<idno type="wicri:Area/Main/Curation">001737</idno>
<idno type="wicri:Area/Main/Exploration">001737</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family</title>
<author><name sortKey="Zirn, Birgit" sort="Zirn, Birgit" uniqKey="Zirn B" first="Birgit" last="Zirn">Birgit Zirn</name>
<affiliation wicri:level="1"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Institut für Humangenetik, Justus‐Liebig‐Universität Giessen, Giessen</wicri:regionArea>
<wicri:noRegion>Giessen</wicri:noRegion>
<wicri:noRegion>Giessen</wicri:noRegion>
</affiliation>
<affiliation wicri:level="3"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Abteilung für Neuropädiatrie, Universität Göttingen, Göttingen</wicri:regionArea>
<placeName><region type="land" nuts="2">Basse-Saxe</region>
<settlement type="city">Göttingen</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Korenke, Christoph" sort="Korenke, Christoph" uniqKey="Korenke C" first="Christoph" last="Korenke">Christoph Korenke</name>
<affiliation wicri:level="1"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Abteilung für Neuropädiatrie, Oldenburg</wicri:regionArea>
<wicri:noRegion>Oldenburg</wicri:noRegion>
<wicri:noRegion>Oldenburg</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Wagner, Michael" sort="Wagner, Michael" uniqKey="Wagner M" first="Michael" last="Wagner">Michael Wagner</name>
<affiliation wicri:level="1"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Sozialpädiatrisches Zentrum, Oldenburg</wicri:regionArea>
<wicri:noRegion>Oldenburg</wicri:noRegion>
<wicri:noRegion>Oldenburg</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Rudnik Choneborn, Sabine" sort="Rudnik Choneborn, Sabine" uniqKey="Rudnik Choneborn S" first="Sabine" last="Rudnik-Schöneborn">Sabine Rudnik-Schöneborn</name>
<affiliation wicri:level="1"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Institut für Humangenetik, RWTH Aachen</wicri:regionArea>
<wicri:noRegion>RWTH Aachen</wicri:noRegion>
<wicri:noRegion>RWTH Aachen</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Muller, Ulrich" sort="Muller, Ulrich" uniqKey="Muller U" first="Ulrich" last="Müller">Ulrich Müller</name>
<affiliation wicri:level="1"><country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Institut für Humangenetik and JLU‐Giessen, bio.logis, Zentrum für Humangenetik, Frankfurt</wicri:regionArea>
<wicri:noRegion>Frankfurt</wicri:noRegion>
<wicri:noRegion>Frankfurt</wicri:noRegion>
</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="2011-02-01">2011-02-01</date>
<biblScope unit="vol">26</biblScope>
<biblScope unit="issue">2</biblScope>
<biblScope unit="page" from="361">361</biblScope>
<biblScope unit="page" to="362">362</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">6FCCD7EB8652F36E37F141DB44C65E8201E45F9E</idno>
<idno type="DOI">10.1002/mds.23437</idno>
<idno type="ArticleID">MDS23437</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Charcot-Marie-Tooth Disease (complications)</term>
<term>Charcot-Marie-Tooth Disease (genetics)</term>
<term>Dystonic Disorders (complications)</term>
<term>Dystonic Disorders (genetics)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Charcot-Marie-Tooth Disease</term>
<term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Charcot-Marie-Tooth Disease</term>
<term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Allemagne</li>
</country>
<region><li>Basse-Saxe</li>
</region>
<settlement><li>Göttingen</li>
</settlement>
</list>
<tree><country name="Allemagne"><noRegion><name sortKey="Zirn, Birgit" sort="Zirn, Birgit" uniqKey="Zirn B" first="Birgit" last="Zirn">Birgit Zirn</name>
</noRegion>
<name sortKey="Korenke, Christoph" sort="Korenke, Christoph" uniqKey="Korenke C" first="Christoph" last="Korenke">Christoph Korenke</name>
<name sortKey="Muller, Ulrich" sort="Muller, Ulrich" uniqKey="Muller U" first="Ulrich" last="Müller">Ulrich Müller</name>
<name sortKey="Rudnik Choneborn, Sabine" sort="Rudnik Choneborn, Sabine" uniqKey="Rudnik Choneborn S" first="Sabine" last="Rudnik-Schöneborn">Sabine Rudnik-Schöneborn</name>
<name sortKey="Wagner, Michael" sort="Wagner, Michael" uniqKey="Wagner M" first="Michael" last="Wagner">Michael Wagner</name>
<name sortKey="Zirn, Birgit" sort="Zirn, Birgit" uniqKey="Zirn B" first="Birgit" last="Zirn">Birgit Zirn</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 001737 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001737 | 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:6FCCD7EB8652F36E37F141DB44C65E8201E45F9E
   |texte=   Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family
}}

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)

Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family

Concurrence of dystonia 1 and Charcot‐Marie‐Tooth Neuropathy, type 1 A, in a large family

Source :

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

	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.