Association of chorea and motor neuron disease.
Identifieur interne : 000744 ( Ncbi/Curation ); précédent : 000743; suivant : 000745Association of chorea and motor neuron disease.
Auteurs : Pierre-François Pradat [France] ; François Salachas ; Lucette Lacomblez ; Nathalie Patte ; Nadine Leforestier ; Véronique Gaura ; Vincent MeiningerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2002.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Chorea, Motor Neuron Disease.
- pathology : Brain.
- Adult, Atrophy, Follow-Up Studies, Humans, Magnetic Resonance Imaging, Male, Neurologic Examination.
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.
PubMed: 11921138
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pubmed:11921138Le document en format XML
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sortKey="Patte, Nathalie" sort="Patte, Nathalie" uniqKey="Patte N" first="Nathalie" last="Patte">Nathalie Patte</name></author><author><name sortKey="Leforestier, Nadine" sort="Leforestier, Nadine" uniqKey="Leforestier N" first="Nadine" last="Leforestier">Nadine Leforestier</name></author><author><name sortKey="Gaura, Veronique" sort="Gaura, Veronique" uniqKey="Gaura V" first="Véronique" last="Gaura">Véronique Gaura</name></author><author><name sortKey="Meininger, Vincent" sort="Meininger, Vincent" uniqKey="Meininger V" first="Vincent" last="Meininger">Vincent Meininger</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2002">2002</date><idno type="RBID">pubmed:11921138</idno><idno type="pmid">11921138</idno><idno type="wicri:Area/PubMed/Corpus">003B07</idno><idno type="wicri:Area/PubMed/Curation">003B07</idno><idno type="wicri:Area/PubMed/Checkpoint">003B89</idno><idno type="wicri:Area/Ncbi/Merge">000744</idno><idno 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last="Lacomblez">Lucette Lacomblez</name></author><author><name sortKey="Patte, Nathalie" sort="Patte, Nathalie" uniqKey="Patte N" first="Nathalie" last="Patte">Nathalie Patte</name></author><author><name sortKey="Leforestier, Nadine" sort="Leforestier, Nadine" uniqKey="Leforestier N" first="Nadine" last="Leforestier">Nadine Leforestier</name></author><author><name sortKey="Gaura, Veronique" sort="Gaura, Veronique" uniqKey="Gaura V" first="Véronique" last="Gaura">Véronique Gaura</name></author><author><name sortKey="Meininger, Vincent" sort="Meininger, Vincent" uniqKey="Meininger V" first="Vincent" last="Meininger">Vincent Meininger</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="ISSN">0885-3185</idno><imprint><date when="2002" type="published">2002</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Atrophy</term><term>Brain (pathology)</term><term>Chorea (diagnosis)</term><term>Follow-Up Studies</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Motor Neuron Disease (diagnosis)</term><term>Neurologic Examination</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Chorea</term><term>Motor Neuron Disease</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Atrophy</term><term>Follow-Up Studies</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Neurologic Examination</term></keywords></textClass></profileDesc></teiHeader><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.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.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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