MovDisordV3, Main, Exploration, bibRecord, 001907

“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update

Identifieur interne : 001907 ( Main/Exploration ); précédent : 001906; suivant : 001908

“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update

Auteurs : Maja Kojovic [Royaume-Uni] ; Mikko Kuoppam Ki [Finlande] ; Niall Quinn [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]

Source :

Movement Disorders [ 0885-3185 ] ; 2010-12-15.

RBID : ISTEX:5781A57D377F1DFFE1D64674BBA92BCBDDF40555

Descripteurs français

Pascal (Inist)
- Dystonie, Mutation, Pathologie du système nerveux.

English descriptors

KwdEn :
- Anoxia (complications), Anoxia (pathology), Brain (pathology), Disease Progression, Dystonia, Dystonic Disorders (etiology), Dystonic Disorders (pathology), Female, Genetic Predisposition to Disease, Humans, Magnetic Field Therapy, Mutation, Nervous system diseases, Neurologic Examination, Phosphotransferases (Alcohol Group Acceptor) (genetics).
MESH :
- chemical , genetics : Phosphotransferases (Alcohol Group Acceptor).
- complications : Anoxia.
- etiology : Dystonic Disorders.
- pathology : Anoxia, Brain, Dystonic Disorders.
- Disease Progression, Female, Genetic Predisposition to Disease, Humans, Magnetic Field Therapy, Mutation, Neurologic Examination.

Url:

https://api.istex.fr/document/5781A57D377F1DFFE1D64674BBA92BCBDDF40555/fulltext/pdf

DOI: 10.1002/mds.23153

Affiliations:

Le document en format XML

<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update</title>
<author><name sortKey="Kojovic, Maja" sort="Kojovic, Maja" uniqKey="Kojovic M" first="Maja" last="Kojovic">Maja Kojovic</name>
</author>
<author><name sortKey="Kuoppam Ki, Mikko" sort="Kuoppam Ki, Mikko" uniqKey="Kuoppam Ki M" first="Mikko" last="Kuoppam Ki">Mikko Kuoppam Ki</name>
</author>
<author><name sortKey="Quinn, Niall" sort="Quinn, Niall" uniqKey="Quinn N" first="Niall" last="Quinn">Niall Quinn</name>
</author>
<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:5781A57D377F1DFFE1D64674BBA92BCBDDF40555</idno>
<date when="2010" year="2010">2010</date>
<idno type="doi">10.1002/mds.23153</idno>
<idno type="url">https://api.istex.fr/document/5781A57D377F1DFFE1D64674BBA92BCBDDF40555/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002757</idno>
<idno type="wicri:Area/Istex/Curation">002757</idno>
<idno type="wicri:Area/Istex/Checkpoint">000586</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Kojovic M:progressive:delayed:onset</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:20925075</idno>
<idno type="wicri:Area/PubMed/Corpus">001527</idno>
<idno type="wicri:Area/PubMed/Curation">001527</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001A92</idno>
<idno type="wicri:Area/Ncbi/Merge">002E90</idno>
<idno type="wicri:Area/Ncbi/Curation">002E90</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002E90</idno>
<idno type="wicri:Area/Main/Merge">001D43</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:11-0065140</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000761</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002557</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000C50</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Kojovic M:progressive:delayed:onset</idno>
<idno type="wicri:Area/Main/Merge">002837</idno>
<idno type="wicri:Area/Main/Curation">001907</idno>
<idno type="wicri:Area/Main/Exploration">001907</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update</title>
<author><name sortKey="Kojovic, Maja" sort="Kojovic, Maja" uniqKey="Kojovic M" first="Maja" last="Kojovic">Maja Kojovic</name>
<affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London</wicri:regionArea>
<placeName><settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Kuoppam Ki, Mikko" sort="Kuoppam Ki, Mikko" uniqKey="Kuoppam Ki M" first="Mikko" last="Kuoppam Ki">Mikko Kuoppam Ki</name>
<affiliation wicri:level="3"><country xml:lang="fr">Finlande</country>
<wicri:regionArea>Orion Pharma, CNS Development, R&D, Turku</wicri:regionArea>
<placeName><settlement type="city">Turku</settlement>
<region type="région" nuts="2">Finlande occidentale</region>
</placeName>
</affiliation>
<affiliation wicri:level="3"><country xml:lang="fr">Finlande</country>
<wicri:regionArea>Department of Neurology, Turku University Hospital, University of Turku, Turku</wicri:regionArea>
<placeName><settlement type="city">Turku</settlement>
<region type="région" nuts="2">Finlande occidentale</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Quinn, Niall" sort="Quinn, Niall" uniqKey="Quinn N" first="Niall" last="Quinn">Niall Quinn</name>
<affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London</wicri:regionArea>
<placeName><settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
<affiliation wicri:level="3"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London</wicri:regionArea>
<placeName><settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</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="2010-12-15">2010-12-15</date>
<biblScope unit="vol">25</biblScope>
<biblScope unit="issue">16</biblScope>
<biblScope unit="page" from="2889">2889</biblScope>
<biblScope unit="page" to="2891">2891</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">5781A57D377F1DFFE1D64674BBA92BCBDDF40555</idno>
<idno type="DOI">10.1002/mds.23153</idno>
<idno type="ArticleID">MDS23153</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anoxia (complications)</term>
<term>Anoxia (pathology)</term>
<term>Brain (pathology)</term>
<term>Disease Progression</term>
<term>Dystonia</term>
<term>Dystonic Disorders (etiology)</term>
<term>Dystonic Disorders (pathology)</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Magnetic Field Therapy</term>
<term>Mutation</term>
<term>Nervous system diseases</term>
<term>Neurologic Examination</term>
<term>Phosphotransferases (Alcohol Group Acceptor) (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Phosphotransferases (Alcohol Group Acceptor)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Anoxia</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Anoxia</term>
<term>Brain</term>
<term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Disease Progression</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Magnetic Field Therapy</term>
<term>Mutation</term>
<term>Neurologic Examination</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dystonie</term>
<term>Mutation</term>
<term>Pathologie du   système nerveux</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Finlande</li>
<li>Royaume-Uni</li>
</country>
<region><li>Angleterre</li>
<li>Finlande occidentale</li>
<li>Grand Londres</li>
</region>
<settlement><li>Londres</li>
<li>Turku</li>
</settlement>
</list>
<tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Kojovic, Maja" sort="Kojovic, Maja" uniqKey="Kojovic M" first="Maja" last="Kojovic">Maja Kojovic</name>
</region>
<name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
<name sortKey="Quinn, Niall" sort="Quinn, Niall" uniqKey="Quinn N" first="Niall" last="Quinn">Niall Quinn</name>
</country>
<country name="Finlande"><region name="Finlande occidentale"><name sortKey="Kuoppam Ki, Mikko" sort="Kuoppam Ki, Mikko" uniqKey="Kuoppam Ki M" first="Mikko" last="Kuoppam Ki">Mikko Kuoppam Ki</name>
</region>
<name sortKey="Kuoppam Ki, Mikko" sort="Kuoppam Ki, Mikko" uniqKey="Kuoppam Ki M" first="Mikko" last="Kuoppam Ki">Mikko Kuoppam Ki</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 001907 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001907 | 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:5781A57D377F1DFFE1D64674BBA92BCBDDF40555
   |texte=   “Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—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)

“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update

“Progressive delayed‐onset postanoxic dystonia” diagnosed with PANK2 mutations 26 years after onset—An update

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

	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.