Association of chorea and motor neuron disease
Identifieur interne : 006894 ( Main/Merge ); précédent : 006893; suivant : 006895Association of chorea and motor neuron disease
Auteurs : Pierre-Francois Pradat [France] ; Francois Salachas [France] ; Stéphanie Cartalat-Carel [France] ; Lucette Lacomblez [France] ; Nathalie Patte [France] ; Nadine Leforestier [France] ; Véronique Gaura [France] ; Vincent Meininger [France]Source :
- Movement disorders [ 0885-3185 ] ; 2002.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
Abstract
Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.1 We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs.
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Pascal:02-0312612Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Association of chorea and motor neuron disease</title>
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<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
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<imprint><date when="2002">2002</date>
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<seriesStmt><title level="j" type="main">Movement disorders</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amyotrophic lateral sclerosis</term>
<term>Case study</term>
<term>Chorea</term>
<term>Concomitant disease</term>
<term>Differential diagnostic</term>
<term>Human</term>
<term>Motor neuron disease</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Video recording</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Chorée syndrome</term>
<term>Neurone moteur maladie</term>
<term>Sclérose latérale amyotrophique</term>
<term>Imagerie RMN</term>
<term>Etude cas</term>
<term>Diagnostic différentiel</term>
<term>Association morbide</term>
<term>Homme</term>
<term>Enregistrement vidéo</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
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<front><div type="abstract" xml:lang="en">Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.<sup>1</sup>
We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs.</div>
</front>
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<tree><country name="France"><noRegion><name sortKey="Pradat, Pierre Francois" sort="Pradat, Pierre Francois" uniqKey="Pradat P" first="Pierre-Francois" last="Pradat">Pierre-Francois Pradat</name>
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<name sortKey="Cartalat Carel, Stephanie" sort="Cartalat Carel, Stephanie" uniqKey="Cartalat Carel S" first="Stéphanie" last="Cartalat-Carel">Stéphanie Cartalat-Carel</name>
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<name sortKey="Leforestier, Nadine" sort="Leforestier, Nadine" uniqKey="Leforestier N" first="Nadine" last="Leforestier">Nadine Leforestier</name>
<name sortKey="Meininger, Vincent" sort="Meininger, Vincent" uniqKey="Meininger V" first="Vincent" last="Meininger">Vincent Meininger</name>
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<name sortKey="Salachas, Francois" sort="Salachas, Francois" uniqKey="Salachas F" first="Francois" last="Salachas">Francois Salachas</name>
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