MovDisordV3, Main, Exploration, bibRecord, 000D79

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.

Identifieur interne : 000D79 ( Main/Exploration ); précédent : 000D78; suivant : 000D80

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.

Auteurs : Aurélie Méneret ; Cyril Mignot ; Isabelle An ; Marie-Odile Habert ; Aurélia Jacquette ; Marie Vidailhet ; Thierry Bienvenu ; Emmanuel Roze

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.

RBID : pubmed:21953941

English descriptors

KwdEn :
- Adult, Athetosis (complications), Athetosis (genetics), Athetosis (pathology), Brain (pathology), Dystonic Disorders (complications), Dystonic Disorders (genetics), Dystonic Disorders (pathology), Female, Forkhead Transcription Factors (genetics), Humans, Magnetic Resonance Imaging, Mutation (genetics), Nerve Tissue Proteins (genetics), Parkinsonian Disorders (complications), Parkinsonian Disorders (genetics), Parkinsonian Disorders (pathology).
MESH :
- chemical , genetics : Forkhead Transcription Factors, Nerve Tissue Proteins.
- complications : Athetosis, Dystonic Disorders, Parkinsonian Disorders.
- genetics : Athetosis, Dystonic Disorders, Mutation, Parkinsonian Disorders.
- pathology : Athetosis, Brain, Dystonic Disorders, Parkinsonian Disorders.
- Adult, Female, Humans, Magnetic Resonance Imaging.

DOI: 10.1002/mds.23956
PubMed: 21953941

Affiliations:

Le document en format XML

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<author><name sortKey="Mignot, Cyril" sort="Mignot, Cyril" uniqKey="Mignot C" first="Cyril" last="Mignot">Cyril Mignot</name>
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<author><name sortKey="An, Isabelle" sort="An, Isabelle" uniqKey="An I" first="Isabelle" last="An">Isabelle An</name>
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<author><name sortKey="Habert, Marie Odile" sort="Habert, Marie Odile" uniqKey="Habert M" first="Marie-Odile" last="Habert">Marie-Odile Habert</name>
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<author><name sortKey="Jacquette, Aurelia" sort="Jacquette, Aurelia" uniqKey="Jacquette A" first="Aurélia" last="Jacquette">Aurélia Jacquette</name>
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<author><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
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<author><name sortKey="Bienvenu, Thierry" sort="Bienvenu, Thierry" uniqKey="Bienvenu T" first="Thierry" last="Bienvenu">Thierry Bienvenu</name>
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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="An, Isabelle" sort="An, Isabelle" uniqKey="An I" first="Isabelle" last="An">Isabelle An</name>
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<author><name sortKey="Habert, Marie Odile" sort="Habert, Marie Odile" uniqKey="Habert M" first="Marie-Odile" last="Habert">Marie-Odile Habert</name>
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<author><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
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<author><name sortKey="Bienvenu, Thierry" sort="Bienvenu, Thierry" uniqKey="Bienvenu T" first="Thierry" last="Bienvenu">Thierry Bienvenu</name>
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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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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Athetosis (complications)</term>
<term>Athetosis (genetics)</term>
<term>Athetosis (pathology)</term>
<term>Brain (pathology)</term>
<term>Dystonic Disorders (complications)</term>
<term>Dystonic Disorders (genetics)</term>
<term>Dystonic Disorders (pathology)</term>
<term>Female</term>
<term>Forkhead Transcription Factors (genetics)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Mutation (genetics)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Parkinsonian Disorders (complications)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Parkinsonian Disorders (pathology)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Forkhead Transcription Factors</term>
<term>Nerve Tissue Proteins</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Athetosis</term>
<term>Dystonic Disorders</term>
<term>Parkinsonian Disorders</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Athetosis</term>
<term>Dystonic Disorders</term>
<term>Mutation</term>
<term>Parkinsonian Disorders</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Athetosis</term>
<term>Brain</term>
<term>Dystonic Disorders</term>
<term>Parkinsonian Disorders</term>
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<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
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<tree><noCountry><name sortKey="An, Isabelle" sort="An, Isabelle" uniqKey="An I" first="Isabelle" last="An">Isabelle An</name>
<name sortKey="Bienvenu, Thierry" sort="Bienvenu, Thierry" uniqKey="Bienvenu T" first="Thierry" last="Bienvenu">Thierry Bienvenu</name>
<name sortKey="Habert, Marie Odile" sort="Habert, Marie Odile" uniqKey="Habert M" first="Marie-Odile" last="Habert">Marie-Odile Habert</name>
<name sortKey="Jacquette, Aurelia" sort="Jacquette, Aurelia" uniqKey="Jacquette A" first="Aurélia" last="Jacquette">Aurélia Jacquette</name>
<name sortKey="Meneret, Aurelie" sort="Meneret, Aurelie" uniqKey="Meneret A" first="Aurélie" last="Méneret">Aurélie Méneret</name>
<name sortKey="Mignot, Cyril" sort="Mignot, Cyril" uniqKey="Mignot C" first="Cyril" last="Mignot">Cyril Mignot</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>
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</record>

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Movement Disorders (revue)

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.

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

Pour générer des pages wiki

	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.