ParkinsonFranceV1, PubMed, Curation, bibRecord, 000670

The multiple faces of the ATP1A3-related dystonic movement disorder.

Identifieur interne : 000670 ( PubMed/Curation ); précédent : 000669; suivant : 000671

The multiple faces of the ATP1A3-related dystonic movement disorder.

Auteurs : Anne Roubergue [France] ; Emmanuel Roze ; Sandrine Vuillaumier-Barrot ; Marie-Joséphine Fontenille ; Aurélie Méneret ; Marie Vidailhet ; Bertrand Fontaine ; Diane Doummar ; Bertrand Philibert ; Florence Riant ; Sophie Nicole

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:23483595

English descriptors

KwdEn :
- Adolescent, Adult, Age of Onset, Child, Preschool, Dystonic Disorders (genetics), Dystonic Disorders (physiopathology), Family, Female, Hemiplegia (genetics), Hemiplegia (physiopathology), Humans, Male, Middle Aged, Mutation (genetics), Parkinson Disease (genetics), Parkinson Disease (physiopathology), Polymerase Chain Reaction, Sodium-Potassium-Exchanging ATPase (genetics), Young Adult.
MESH :
- chemical , genetics : Sodium-Potassium-Exchanging ATPase.
- genetics : Dystonic Disorders, Hemiplegia, Mutation, Parkinson Disease.
- physiopathology : Dystonic Disorders, Hemiplegia, Parkinson Disease.
- Adolescent, Adult, Age of Onset, Child, Preschool, Family, Female, Humans, Male, Middle Aged, Polymerase Chain Reaction, Young Adult.

DOI: 10.1002/mds.25396
PubMed: 23483595

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pubmed:23483595

Le document en format XML

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<affiliation wicri:level="1"><nlm:affiliation>AP-HP, Service de Neuropédiatrie, Hôpital Armand Trousseau Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>AP-HP, Service de Neuropédiatrie, Hôpital Armand Trousseau Paris</wicri:regionArea>
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<author><name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name>
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<author><name sortKey="Vuillaumier Barrot, Sandrine" sort="Vuillaumier Barrot, Sandrine" uniqKey="Vuillaumier Barrot S" first="Sandrine" last="Vuillaumier-Barrot">Sandrine Vuillaumier-Barrot</name>
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<author><name sortKey="Fontenille, Marie Josephine" sort="Fontenille, Marie Josephine" uniqKey="Fontenille M" first="Marie-Joséphine" last="Fontenille">Marie-Joséphine Fontenille</name>
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<author><name sortKey="Meneret, Aurelie" sort="Meneret, Aurelie" uniqKey="Meneret A" first="Aurélie" last="Méneret">Aurélie Méneret</name>
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<author><name sortKey="Fontaine, Bertrand" sort="Fontaine, Bertrand" uniqKey="Fontaine B" first="Bertrand" last="Fontaine">Bertrand Fontaine</name>
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<author><name sortKey="Doummar, Diane" sort="Doummar, Diane" uniqKey="Doummar D" first="Diane" last="Doummar">Diane Doummar</name>
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<author><name sortKey="Philibert, Bertrand" sort="Philibert, Bertrand" uniqKey="Philibert B" first="Bertrand" last="Philibert">Bertrand Philibert</name>
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<author><name sortKey="Fontenille, Marie Josephine" sort="Fontenille, Marie Josephine" uniqKey="Fontenille M" first="Marie-Joséphine" last="Fontenille">Marie-Joséphine Fontenille</name>
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<author><name sortKey="Doummar, Diane" sort="Doummar, Diane" uniqKey="Doummar D" first="Diane" last="Doummar">Diane Doummar</name>
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<author><name sortKey="Philibert, Bertrand" sort="Philibert, Bertrand" uniqKey="Philibert B" first="Bertrand" last="Philibert">Bertrand Philibert</name>
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<author><name sortKey="Riant, Florence" sort="Riant, Florence" uniqKey="Riant F" first="Florence" last="Riant">Florence Riant</name>
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<author><name sortKey="Nicole, Sophie" sort="Nicole, Sophie" uniqKey="Nicole S" first="Sophie" last="Nicole">Sophie Nicole</name>
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<term>Dystonic Disorders (physiopathology)</term>
<term>Family</term>
<term>Female</term>
<term>Hemiplegia (genetics)</term>
<term>Hemiplegia (physiopathology)</term>
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<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (physiopathology)</term>
<term>Polymerase Chain Reaction</term>
<term>Sodium-Potassium-Exchanging ATPase (genetics)</term>
<term>Young Adult</term>
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<term>Hemiplegia</term>
<term>Mutation</term>
<term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Dystonic Disorders</term>
<term>Hemiplegia</term>
<term>Parkinson Disease</term>
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<term>Adult</term>
<term>Age of Onset</term>
<term>Child, Preschool</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>The multiple faces of the ATP1A3-related dystonic movement disorder.</ArticleTitle>
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<Author ValidYN="Y"><LastName>Méneret</LastName>
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<ChemicalList><Chemical><RegistryNumber>EC 3.6.3.9</RegistryNumber>
<NameOfSubstance UI="C488756">ATP1A3 protein, human</NameOfSubstance>
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The multiple faces of the ATP1A3-related dystonic movement disorder.

The multiple faces of the ATP1A3-related dystonic movement disorder.

Source :

English descriptors

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

Links to Exploration step

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