Serveur d'exploration sur le patient édenté

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.

SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report

Identifieur interne : 002F17 ( Istex/Corpus ); précédent : 002F16; suivant : 002F18

SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report

Auteurs : Alastair Wilkins ; Jerry M. Brown ; Roger A. Barker

Source :

RBID : ISTEX:60163DD9E3887A992F60E772EFEFFCCE890DA0E7

English descriptors

Abstract

We report on a young woman from the United Kingdom with L‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society

Url:
DOI: 10.1002/mds.10715

Links to Exploration step

ISTEX:60163DD9E3887A992F60E772EFEFFCCE890DA0E7

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report</title>
<author>
<name sortKey="Wilkins, Alastair" sort="Wilkins, Alastair" uniqKey="Wilkins A" first="Alastair" last="Wilkins">Alastair Wilkins</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Brown, Jerry M" sort="Brown, Jerry M" uniqKey="Brown J" first="Jerry M." last="Brown">Jerry M. Brown</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Barker, Roger A" sort="Barker, Roger A" uniqKey="Barker R" first="Roger A." last="Barker">Roger A. Barker</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>E-mail: rab46@cus.cam.ac.uk</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Correspondence address: Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:60163DD9E3887A992F60E772EFEFFCCE890DA0E7</idno>
<date when="2004" year="2004">2004</date>
<idno type="doi">10.1002/mds.10715</idno>
<idno type="url">https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002F17</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002F17</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
<ref type="note" target="#fn1"></ref>
</title>
<author>
<name sortKey="Wilkins, Alastair" sort="Wilkins, Alastair" uniqKey="Wilkins A" first="Alastair" last="Wilkins">Alastair Wilkins</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Brown, Jerry M" sort="Brown, Jerry M" uniqKey="Brown J" first="Jerry M." last="Brown">Jerry M. Brown</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Barker, Roger A" sort="Barker, Roger A" uniqKey="Barker R" first="Roger A." last="Barker">Roger A. Barker</name>
<affiliation>
<mods:affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>E-mail: rab46@cus.cam.ac.uk</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Correspondence address: Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</mods:affiliation>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j" type="main">Movement Disorders</title>
<title level="j" type="alt">MOVEMENT DISORDERS</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<biblScope unit="vol">19</biblScope>
<biblScope unit="issue">5</biblScope>
<biblScope unit="page" from="593">593</biblScope>
<biblScope unit="page" to="595">595</biblScope>
<biblScope unit="page-count">2</biblScope>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2004-05">2004-05</date>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Abnormal</term>
<term>Abnormal activity</term>
<term>Abnormal movements</term>
<term>Acta</term>
<term>Acta neuropathol</term>
<term>Allele</term>
<term>Anterocollis</term>
<term>Ataxia</term>
<term>Atrophy</term>
<term>Autosomal</term>
<term>Axial right</term>
<term>Basal</term>
<term>Basal ganglia</term>
<term>Biceps brachii</term>
<term>Bilateral</term>
<term>Bilateral stimulation</term>
<term>Bilaterally</term>
<term>Botox</term>
<term>Botulinum</term>
<term>Botulinum toxin</term>
<term>Botulinum toxin type</term>
<term>Bradykinesia</term>
<term>Case report</term>
<term>Caudate</term>
<term>Caudate nucleus</term>
<term>Cerebellar</term>
<term>Cerebellar ataxia</term>
<term>Cervical</term>
<term>Cervical dystonia</term>
<term>Chorea</term>
<term>Choreic movements</term>
<term>Choreiform</term>
<term>Choreiform movements</term>
<term>Clinical features</term>
<term>Clinical outcome</term>
<term>Cogwheel rigidity</term>
<term>Colli</term>
<term>Contralateral</term>
<term>Cyclohydrolase</term>
<term>Deep brain stimulation</term>
<term>Degenerative ataxias</term>
<term>Dentatorubral</term>
<term>Dentatorubral pallidoluysian atrophy</term>
<term>Disord</term>
<term>Disorder</term>
<term>Dopamine</term>
<term>Drpla</term>
<term>Dyskinesia</term>
<term>Dystonia</term>
<term>Dystonic</term>
<term>Dystonic posture</term>
<term>Extrapyramidal</term>
<term>Familial cases</term>
<term>Family history</term>
<term>Ganglion</term>
<term>Genet</term>
<term>Genetic studies</term>
<term>Globus</term>
<term>Globus pallidum</term>
<term>Globus pallidus</term>
<term>Globus pallidus internus</term>
<term>Hereditary</term>
<term>Imaging</term>
<term>Inclusion</term>
<term>Interscience</term>
<term>Intramuscular</term>
<term>Intranuclear</term>
<term>Intranuclear inclusions</term>
<term>Involuntary movements</term>
<term>Jerk</term>
<term>Lancet</term>
<term>Longus</term>
<term>Longus colli</term>
<term>Magnetic resonance imaging</term>
<term>Moderate improvement</term>
<term>Movement disorder society</term>
<term>Movement disorders</term>
<term>Mutant</term>
<term>Mutation</term>
<term>Myoclonus</term>
<term>Nding</term>
<term>Ndings</term>
<term>Neurol</term>
<term>Neurol neurosurg psychiatry</term>
<term>Neurological</term>
<term>Neurology</term>
<term>Neuron</term>
<term>Neuronal</term>
<term>Neuropathological</term>
<term>Neuropathological features</term>
<term>Neurosurg</term>
<term>Normal values</term>
<term>October</term>
<term>Online</term>
<term>Oromandibular dystonia</term>
<term>Pallidal</term>
<term>Pallidal stimulation</term>
<term>Pallidoluysian</term>
<term>Pallidum</term>
<term>Pallidus</term>
<term>Parkinsonism</term>
<term>Perfusion</term>
<term>Phenotype</term>
<term>Propriospinal</term>
<term>Propriospinal myoclonus</term>
<term>Puncture site</term>
<term>Putamen</term>
<term>Radcliffe oxford</term>
<term>Rectus</term>
<term>Rectus abdominis</term>
<term>Rectus femoris</term>
<term>Right longus colli muscle</term>
<term>Rinsho shinkeigaku</term>
<term>Sca1</term>
<term>Sca2</term>
<term>Sca2 allele</term>
<term>Senile chorea</term>
<term>Several years</term>
<term>Severe anterocollis</term>
<term>Side effects</term>
<term>Single photon emission tomography</term>
<term>Spasmodic torticollis</term>
<term>Spet</term>
<term>Spinal</term>
<term>Spinocerebellar</term>
<term>Spinocerebellar ataxia</term>
<term>Spinocerebellar ataxia type</term>
<term>Sporadic case</term>
<term>Sporadic cases</term>
<term>Sternocleidomastoid</term>
<term>Sternocleidomastoid muscle</term>
<term>Sternocleidomastoid muscles</term>
<term>Sternocleidomastoideus</term>
<term>Stimulation</term>
<term>Stimulator</term>
<term>Subthalamic</term>
<term>Subthalamic nucleus</term>
<term>Symptom</term>
<term>Tardive</term>
<term>Tardive dyskinesia</term>
<term>Thalamic</term>
<term>Thalamic stimulation</term>
<term>Thalamus</term>
<term>Tohoku university school</term>
<term>Tomography</term>
<term>Torticollis</term>
<term>Toxin</term>
<term>Tremor</term>
<term>Trinucleotide</term>
<term>Trinucleotide expansion</term>
<term>Unilateral stimulation</term>
<term>Ventralis oralis</term>
<term>Video</term>
<term>Video segment</term>
<term>Videotape</term>
<term>Wiley interscience</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en">
<term>Abnormal</term>
<term>Abnormal activity</term>
<term>Abnormal movements</term>
<term>Acta</term>
<term>Acta neuropathol</term>
<term>Allele</term>
<term>Anterocollis</term>
<term>Ataxia</term>
<term>Atrophy</term>
<term>Autosomal</term>
<term>Axial right</term>
<term>Basal</term>
<term>Basal ganglia</term>
<term>Biceps brachii</term>
<term>Bilateral</term>
<term>Bilateral stimulation</term>
<term>Bilaterally</term>
<term>Botox</term>
<term>Botulinum</term>
<term>Botulinum toxin</term>
<term>Botulinum toxin type</term>
<term>Bradykinesia</term>
<term>Case report</term>
<term>Caudate</term>
<term>Caudate nucleus</term>
<term>Cerebellar</term>
<term>Cerebellar ataxia</term>
<term>Cervical</term>
<term>Cervical dystonia</term>
<term>Chorea</term>
<term>Choreic movements</term>
<term>Choreiform</term>
<term>Choreiform movements</term>
<term>Clinical features</term>
<term>Clinical outcome</term>
<term>Cogwheel rigidity</term>
<term>Colli</term>
<term>Contralateral</term>
<term>Cyclohydrolase</term>
<term>Deep brain stimulation</term>
<term>Degenerative ataxias</term>
<term>Dentatorubral</term>
<term>Dentatorubral pallidoluysian atrophy</term>
<term>Disord</term>
<term>Disorder</term>
<term>Dopamine</term>
<term>Drpla</term>
<term>Dyskinesia</term>
<term>Dystonia</term>
<term>Dystonic</term>
<term>Dystonic posture</term>
<term>Extrapyramidal</term>
<term>Familial cases</term>
<term>Family history</term>
<term>Ganglion</term>
<term>Genet</term>
<term>Genetic studies</term>
<term>Globus</term>
<term>Globus pallidum</term>
<term>Globus pallidus</term>
<term>Globus pallidus internus</term>
<term>Hereditary</term>
<term>Imaging</term>
<term>Inclusion</term>
<term>Interscience</term>
<term>Intramuscular</term>
<term>Intranuclear</term>
<term>Intranuclear inclusions</term>
<term>Involuntary movements</term>
<term>Jerk</term>
<term>Lancet</term>
<term>Longus</term>
<term>Longus colli</term>
<term>Magnetic resonance imaging</term>
<term>Moderate improvement</term>
<term>Movement disorder society</term>
<term>Movement disorders</term>
<term>Mutant</term>
<term>Mutation</term>
<term>Myoclonus</term>
<term>Nding</term>
<term>Ndings</term>
<term>Neurol</term>
<term>Neurol neurosurg psychiatry</term>
<term>Neurological</term>
<term>Neurology</term>
<term>Neuron</term>
<term>Neuronal</term>
<term>Neuropathological</term>
<term>Neuropathological features</term>
<term>Neurosurg</term>
<term>Normal values</term>
<term>October</term>
<term>Online</term>
<term>Oromandibular dystonia</term>
<term>Pallidal</term>
<term>Pallidal stimulation</term>
<term>Pallidoluysian</term>
<term>Pallidum</term>
<term>Pallidus</term>
<term>Parkinsonism</term>
<term>Perfusion</term>
<term>Phenotype</term>
<term>Propriospinal</term>
<term>Propriospinal myoclonus</term>
<term>Puncture site</term>
<term>Putamen</term>
<term>Radcliffe oxford</term>
<term>Rectus</term>
<term>Rectus abdominis</term>
<term>Rectus femoris</term>
<term>Right longus colli muscle</term>
<term>Rinsho shinkeigaku</term>
<term>Sca1</term>
<term>Sca2</term>
<term>Sca2 allele</term>
<term>Senile chorea</term>
<term>Several years</term>
<term>Severe anterocollis</term>
<term>Side effects</term>
<term>Single photon emission tomography</term>
<term>Spasmodic torticollis</term>
<term>Spet</term>
<term>Spinal</term>
<term>Spinocerebellar</term>
<term>Spinocerebellar ataxia</term>
<term>Spinocerebellar ataxia type</term>
<term>Sporadic case</term>
<term>Sporadic cases</term>
<term>Sternocleidomastoid</term>
<term>Sternocleidomastoid muscle</term>
<term>Sternocleidomastoid muscles</term>
<term>Sternocleidomastoideus</term>
<term>Stimulation</term>
<term>Stimulator</term>
<term>Subthalamic</term>
<term>Subthalamic nucleus</term>
<term>Symptom</term>
<term>Tardive</term>
<term>Tardive dyskinesia</term>
<term>Thalamic</term>
<term>Thalamic stimulation</term>
<term>Thalamus</term>
<term>Tohoku university school</term>
<term>Tomography</term>
<term>Torticollis</term>
<term>Toxin</term>
<term>Tremor</term>
<term>Trinucleotide</term>
<term>Trinucleotide expansion</term>
<term>Unilateral stimulation</term>
<term>Ventralis oralis</term>
<term>Video</term>
<term>Video segment</term>
<term>Videotape</term>
<term>Wiley interscience</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">We report on a young woman from the United Kingdom with L‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society</div>
</front>
</TEI>
<istex>
<corpusName>wiley</corpusName>
<keywords>
<teeft>
<json:string>dystonia</json:string>
<json:string>ataxia</json:string>
<json:string>neurol</json:string>
<json:string>dyskinesia</json:string>
<json:string>chorea</json:string>
<json:string>movement disorders</json:string>
<json:string>neurology</json:string>
<json:string>mutation</json:string>
<json:string>parkinsonism</json:string>
<json:string>sca2</json:string>
<json:string>basal</json:string>
<json:string>spet</json:string>
<json:string>spinocerebellar</json:string>
<json:string>myoclonus</json:string>
<json:string>anterocollis</json:string>
<json:string>drpla</json:string>
<json:string>ganglion</json:string>
<json:string>cerebellar</json:string>
<json:string>globus</json:string>
<json:string>longus</json:string>
<json:string>pallidal</json:string>
<json:string>propriospinal</json:string>
<json:string>phenotype</json:string>
<json:string>tardive</json:string>
<json:string>trinucleotide</json:string>
<json:string>sca1</json:string>
<json:string>cervical</json:string>
<json:string>thalamic</json:string>
<json:string>colli</json:string>
<json:string>botox</json:string>
<json:string>botulinum toxin</json:string>
<json:string>intranuclear</json:string>
<json:string>disord</json:string>
<json:string>contralateral</json:string>
<json:string>deep brain stimulation</json:string>
<json:string>dystonic</json:string>
<json:string>pallidus</json:string>
<json:string>ndings</json:string>
<json:string>spinal</json:string>
<json:string>nding</json:string>
<json:string>neurosurg</json:string>
<json:string>tomography</json:string>
<json:string>torticollis</json:string>
<json:string>spinocerebellar ataxia type</json:string>
<json:string>allele</json:string>
<json:string>october</json:string>
<json:string>extrapyramidal</json:string>
<json:string>putamen</json:string>
<json:string>neuropathological</json:string>
<json:string>propriospinal myoclonus</json:string>
<json:string>dopamine</json:string>
<json:string>cyclohydrolase</json:string>
<json:string>perfusion</json:string>
<json:string>subthalamic</json:string>
<json:string>sternocleidomastoid</json:string>
<json:string>rectus</json:string>
<json:string>neurol neurosurg psychiatry</json:string>
<json:string>pallidum</json:string>
<json:string>autosomal</json:string>
<json:string>cervical dystonia</json:string>
<json:string>sternocleidomastoideus</json:string>
<json:string>toxin</json:string>
<json:string>botulinum</json:string>
<json:string>bradykinesia</json:string>
<json:string>videotape</json:string>
<json:string>tardive dyskinesia</json:string>
<json:string>side effects</json:string>
<json:string>stimulator</json:string>
<json:string>wiley interscience</json:string>
<json:string>online</json:string>
<json:string>choreiform</json:string>
<json:string>movement disorder society</json:string>
<json:string>mutant</json:string>
<json:string>pallidoluysian</json:string>
<json:string>lancet</json:string>
<json:string>acta</json:string>
<json:string>bilaterally</json:string>
<json:string>subthalamic nucleus</json:string>
<json:string>basal ganglia</json:string>
<json:string>intramuscular</json:string>
<json:string>dentatorubral</json:string>
<json:string>caudate</json:string>
<json:string>genet</json:string>
<json:string>thalamus</json:string>
<json:string>neurological</json:string>
<json:string>spinocerebellar ataxia</json:string>
<json:string>magnetic resonance imaging</json:string>
<json:string>sternocleidomastoid muscles</json:string>
<json:string>intranuclear inclusions</json:string>
<json:string>rinsho shinkeigaku</json:string>
<json:string>family history</json:string>
<json:string>spasmodic torticollis</json:string>
<json:string>ventralis oralis</json:string>
<json:string>globus pallidus internus</json:string>
<json:string>thalamic stimulation</json:string>
<json:string>senile chorea</json:string>
<json:string>longus colli</json:string>
<json:string>case report</json:string>
<json:string>severe anterocollis</json:string>
<json:string>caudate nucleus</json:string>
<json:string>video</json:string>
<json:string>jerk</json:string>
<json:string>pallidal stimulation</json:string>
<json:string>acta neuropathol</json:string>
<json:string>video segment</json:string>
<json:string>rectus abdominis</json:string>
<json:string>sporadic cases</json:string>
<json:string>globus pallidum</json:string>
<json:string>sporadic case</json:string>
<json:string>dystonic posture</json:string>
<json:string>involuntary movements</json:string>
<json:string>oromandibular dystonia</json:string>
<json:string>dentatorubral pallidoluysian atrophy</json:string>
<json:string>disorder</json:string>
<json:string>interscience</json:string>
<json:string>neuronal</json:string>
<json:string>hereditary</json:string>
<json:string>bilateral</json:string>
<json:string>imaging</json:string>
<json:string>neuron</json:string>
<json:string>sternocleidomastoid muscle</json:string>
<json:string>genetic studies</json:string>
<json:string>puncture site</json:string>
<json:string>botulinum toxin type</json:string>
<json:string>trinucleotide expansion</json:string>
<json:string>moderate improvement</json:string>
<json:string>neuropathological features</json:string>
<json:string>familial cases</json:string>
<json:string>clinical outcome</json:string>
<json:string>clinical features</json:string>
<json:string>tohoku university school</json:string>
<json:string>degenerative ataxias</json:string>
<json:string>bilateral stimulation</json:string>
<json:string>choreic movements</json:string>
<json:string>cerebellar ataxia</json:string>
<json:string>several years</json:string>
<json:string>normal values</json:string>
<json:string>sca2 allele</json:string>
<json:string>cogwheel rigidity</json:string>
<json:string>globus pallidus</json:string>
<json:string>right longus colli muscle</json:string>
<json:string>biceps brachii</json:string>
<json:string>abnormal activity</json:string>
<json:string>axial right</json:string>
<json:string>rectus femoris</json:string>
<json:string>abnormal movements</json:string>
<json:string>radcliffe oxford</json:string>
<json:string>choreiform movements</json:string>
<json:string>single photon emission tomography</json:string>
<json:string>unilateral stimulation</json:string>
<json:string>symptom</json:string>
<json:string>inclusion</json:string>
<json:string>atrophy</json:string>
<json:string>stimulation</json:string>
<json:string>tremor</json:string>
<json:string>abnormal</json:string>
</teeft>
</keywords>
<author>
<json:item>
<name>Alastair Wilkins PhD, MRCP</name>
<affiliations>
<json:string>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</json:string>
</affiliations>
</json:item>
<json:item>
<name>Jerry M. Brown MD, MRCP</name>
<affiliations>
<json:string>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</json:string>
</affiliations>
</json:item>
<json:item>
<name>Roger A. Barker PhD, MRCP</name>
<affiliations>
<json:string>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</json:string>
<json:string>E-mail: rab46@cus.cam.ac.uk</json:string>
<json:string>Correspondence address: Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</json:string>
</affiliations>
</json:item>
</author>
<subject>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>SCA2</value>
</json:item>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>parkinsonism</value>
</json:item>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>levodopa</value>
</json:item>
</subject>
<articleId>
<json:string>MDS10715</json:string>
</articleId>
<arkIstex>ark:/67375/WNG-HCNJDV2R-1</arkIstex>
<language>
<json:string>eng</json:string>
</language>
<originalGenre>
<json:string>shortCommunication</json:string>
</originalGenre>
<abstract>We report on a young woman from the United Kingdom with L‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society</abstract>
<qualityIndicators>
<refBibsNative>true</refBibsNative>
<abstractWordCount>52</abstractWordCount>
<abstractCharCount>356</abstractCharCount>
<keywordCount>3</keywordCount>
<score>7.624</score>
<pdfWordCount>15014</pdfWordCount>
<pdfCharCount>98428</pdfCharCount>
<pdfVersion>1.3</pdfVersion>
<pdfPageCount>23</pdfPageCount>
<pdfPageSize>612 x 810 pts</pdfPageSize>
</qualityIndicators>
<title>SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report</title>
<pmid>
<json:string>15133829</json:string>
</pmid>
<genre>
<json:string>brief-communication</json:string>
</genre>
<host>
<title>Movement Disorders</title>
<language>
<json:string>unknown</json:string>
</language>
<doi>
<json:string>10.1002/(ISSN)1531-8257</json:string>
</doi>
<issn>
<json:string>0885-3185</json:string>
</issn>
<eissn>
<json:string>1531-8257</json:string>
</eissn>
<publisherId>
<json:string>MDS</json:string>
</publisherId>
<volume>19</volume>
<issue>5</issue>
<pages>
<first>593</first>
<last>595</last>
<total>2</total>
</pages>
<genre>
<json:string>journal</json:string>
</genre>
<subject>
<json:item>
<value>Clinical/Scientific Note with Video</value>
</json:item>
</subject>
</host>
<namedEntities>
<unitex>
<date>
<json:string>1994</json:string>
<json:string>1984</json:string>
<json:string>2004</json:string>
</date>
<geogName></geogName>
<orgName>
<json:string>University of Toronto</json:string>
<json:string>Department of Pathology</json:string>
<json:string>Department of Laboratory Medicine</json:string>
<json:string>Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada Abstract</json:string>
<json:string>Toronto Western Hospital, Toronto, ON, Canada</json:string>
</orgName>
<orgName_funder></orgName_funder>
<orgName_provider></orgName_provider>
<persName>
<json:string>Iizuka</json:string>
<json:string>Anthony E. Lang</json:string>
<json:string>Catherine Bergeron</json:string>
</persName>
<placeName>
<json:string>Canada</json:string>
</placeName>
<ref_url></ref_url>
<ref_bibl></ref_bibl>
<bibl></bibl>
</unitex>
</namedEntities>
<ark>
<json:string>ark:/67375/WNG-HCNJDV2R-1</json:string>
</ark>
<categories>
<wos>
<json:string>1 - science</json:string>
<json:string>2 - clinical neurology</json:string>
</wos>
<scienceMetrix>
<json:string>1 - health sciences</json:string>
<json:string>2 - clinical medicine</json:string>
<json:string>3 - neurology & neurosurgery</json:string>
</scienceMetrix>
<scopus>
<json:string>1 - Health Sciences</json:string>
<json:string>2 - Medicine</json:string>
<json:string>3 - Clinical Neurology</json:string>
<json:string>1 - Life Sciences</json:string>
<json:string>2 - Neuroscience</json:string>
<json:string>3 - Neurology</json:string>
</scopus>
<inist>
<json:string>1 - sciences appliquees, technologies et medecines</json:string>
<json:string>2 - sciences biologiques et medicales</json:string>
<json:string>3 - sciences medicales</json:string>
<json:string>4 - neurologie</json:string>
</inist>
</categories>
<publicationDate>2004</publicationDate>
<copyrightDate>2004</copyrightDate>
<doi>
<json:string>10.1002/mds.10715</json:string>
</doi>
<id>60163DD9E3887A992F60E772EFEFFCCE890DA0E7</id>
<score>1</score>
<fulltext>
<json:item>
<extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/fulltext/pdf</uri>
</json:item>
<json:item>
<extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/fulltext/tei">
<teiHeader>
<fileDesc>
<titleStmt>
<title level="a" type="main" xml:lang="en">SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
<ref type="note" target="#fn1"></ref>
</title>
</titleStmt>
<publicationStmt>
<authority>ISTEX</authority>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<availability>
<licence>Copyright © 2004 Movement Disorder Society</licence>
</availability>
<date type="published" when="2004-05"></date>
</publicationStmt>
<notesStmt>
<note type="content-type" subtype="brief-communication" source="shortCommunication" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-S9SX2MFS-0">brief-communication</note>
<note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note>
</notesStmt>
<sourceDesc>
<biblStruct type="brief-communication">
<analytic>
<title level="a" type="main" xml:lang="en">SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
<ref type="note" target="#fn1"></ref>
</title>
<title level="a" type="short" xml:lang="en">Clinical/Scientific Notes</title>
<author xml:id="author-0000">
<persName>
<forename type="first">Alastair</forename>
<surname>Wilkins</surname>
<roleName type="degree">PhD, MRCP</roleName>
</persName>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom
<address>
<country key="GB"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0001">
<persName>
<forename type="first">Jerry M.</forename>
<surname>Brown</surname>
<roleName type="degree">MD, MRCP</roleName>
</persName>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom
<address>
<country key="GB"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0002" role="corresp">
<persName>
<forename type="first">Roger A.</forename>
<surname>Barker</surname>
<roleName type="degree">PhD, MRCP</roleName>
</persName>
<email>rab46@cus.cam.ac.uk</email>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom
<address>
<country key="GB"></country>
</address>
</affiliation>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</affiliation>
</author>
<idno type="istex">60163DD9E3887A992F60E772EFEFFCCE890DA0E7</idno>
<idno type="ark">ark:/67375/WNG-HCNJDV2R-1</idno>
<idno type="DOI">10.1002/mds.10715</idno>
<idno type="unit">MDS10715</idno>
<idno type="toTypesetVersion">file:MDS.MDS10715.pdf</idno>
</analytic>
<monogr>
<title level="j" type="main">Movement Disorders</title>
<title level="j" type="alt">MOVEMENT DISORDERS</title>
<idno type="pISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<idno type="book-DOI">10.1002/(ISSN)1531-8257</idno>
<idno type="book-part-DOI">10.1002/mds.v19:5</idno>
<idno type="product">MDS</idno>
<imprint>
<biblScope unit="vol">19</biblScope>
<biblScope unit="issue">5</biblScope>
<biblScope unit="page" from="593">593</biblScope>
<biblScope unit="page" to="595">595</biblScope>
<biblScope unit="page-count">2</biblScope>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2004-05"></date>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<abstract xml:lang="en" style="main">
<head>Abstract</head>
<p>We report on a young woman from the United Kingdom with
<hi rend="smallCaps">L</hi>
‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society</p>
</abstract>
<textClass>
<keywords xml:lang="en">
<term xml:id="kwd1">SCA2</term>
<term xml:id="kwd2">parkinsonism</term>
<term xml:id="kwd3">levodopa</term>
</keywords>
<keywords rend="articleCategory">
<term>Clinical/Scientific Note with Video</term>
</keywords>
<keywords rend="tocHeading1">
<term>Clinical/Scientific Notes</term>
</keywords>
</textClass>
<langUsage>
<language ident="en"></language>
</langUsage>
</profileDesc>
</teiHeader>
</istex:fulltextTEI>
<json:item>
<extension>txt</extension>
<original>false</original>
<mimetype>text/plain</mimetype>
<uri>https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/fulltext/txt</uri>
</json:item>
</fulltext>
<metadata>
<istex:metadataXml wicri:clean="Wiley, elements deleted: body">
<istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration>
<istex:document>
<component version="2.0" type="serialArticle" xml:lang="en">
<header>
<publicationMeta level="product">
<publisherInfo>
<publisherName>Wiley Subscription Services, Inc., A Wiley Company</publisherName>
<publisherLoc>Hoboken</publisherLoc>
</publisherInfo>
<doi registered="yes">10.1002/(ISSN)1531-8257</doi>
<issn type="print">0885-3185</issn>
<issn type="electronic">1531-8257</issn>
<idGroup>
<id type="product" value="MDS"></id>
</idGroup>
<titleGroup>
<title type="main" xml:lang="en" sort="MOVEMENT DISORDERS">Movement Disorders</title>
<title type="subtitle">Official Journal of the Movement Disorder Society</title>
<title type="short">Mov. Disord.</title>
</titleGroup>
</publicationMeta>
<publicationMeta level="part" position="50">
<doi origin="wiley" registered="yes">10.1002/mds.v19:5</doi>
<numberingGroup>
<numbering type="journalVolume" number="19">19</numbering>
<numbering type="journalIssue">5</numbering>
</numberingGroup>
<coverDate startDate="2004-05">May 2004</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="shortCommunication" position="190" status="forIssue">
<doi origin="wiley" registered="yes">10.1002/mds.10715</doi>
<idGroup>
<id type="unit" value="MDS10715"></id>
</idGroup>
<countGroup>
<count type="pageTotal" number="2"></count>
</countGroup>
<titleGroup>
<title type="articleCategory">Clinical/Scientific Note with Video</title>
<title type="tocHeading1">Clinical/Scientific Notes</title>
</titleGroup>
<copyright ownership="thirdParty">Copyright © 2004 Movement Disorder Society</copyright>
<eventGroup>
<event type="manuscriptReceived" date="2003-07-06"></event>
<event type="manuscriptRevised" date="2003-10-10"></event>
<event type="manuscriptAccepted" date="2003-10-21"></event>
<event type="publishedOnlineEarlyUnpaginated" date="2004-01-05"></event>
<event type="firstOnline" date="2004-01-05"></event>
<event type="publishedOnlineFinalForm" date="2004-05-03"></event>
<event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-09"></event>
<event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-02"></event>
<event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-31"></event>
</eventGroup>
<numberingGroup>
<numbering type="pageFirst">593</numbering>
<numbering type="pageLast">595</numbering>
</numberingGroup>
<correspondenceTo>Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</correspondenceTo>
<linkGroup>
<link type="toTypesetVersion" href="file:MDS.MDS10715.pdf"></link>
</linkGroup>
</publicationMeta>
<contentMeta>
<countGroup>
<count type="figureTotal" number="0"></count>
<count type="tableTotal" number="0"></count>
<count type="referenceTotal" number="8"></count>
<count type="wordTotal" number="1192"></count>
</countGroup>
<titleGroup>
<title type="main" xml:lang="en">SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
<link href="#fn1"></link>
</title>
<title type="short" xml:lang="en">Clinical/Scientific Notes</title>
</titleGroup>
<creators>
<creator xml:id="au1" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Alastair</givenNames>
<familyName>Wilkins</familyName>
<degrees>PhD, MRCP</degrees>
</personName>
</creator>
<creator xml:id="au2" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Jerry M.</givenNames>
<familyName>Brown</familyName>
<degrees>MD, MRCP</degrees>
</personName>
</creator>
<creator xml:id="au3" creatorRole="author" affiliationRef="#af1" corresponding="yes">
<personName>
<givenNames>Roger A.</givenNames>
<familyName>Barker</familyName>
<degrees>PhD, MRCP</degrees>
</personName>
<contactDetails>
<email>rab46@cus.cam.ac.uk</email>
</contactDetails>
</creator>
</creators>
<affiliationGroup>
<affiliation xml:id="af1" countryCode="GB" type="organization">
<unparsedAffiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en" type="author">
<keyword xml:id="kwd1">SCA2</keyword>
<keyword xml:id="kwd2">parkinsonism</keyword>
<keyword xml:id="kwd3">levodopa</keyword>
</keywordGroup>
<supportingInformation>
<p> This article contains supplementary video clips, available online at
<url href="http://www.interscience.wiley.com/jpages/0885-3185/suppmat"> http://www.interscience.wiley.com/jpages/0885‐3185/suppmat </url>
</p>
<supportingInfoItem>
<mediaResource alt="supporting information" href="urn-x:wiley:08853185:media:mds10715:suppmat_593"></mediaResource>
<caption>Supporting Information file suppmat_593.mpg</caption>
</supportingInfoItem>
</supportingInformation>
<abstractGroup>
<abstract type="main" xml:lang="en">
<title type="main">Abstract</title>
<p>We report on a young woman from the United Kingdom with
<sc>L</sc>
‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society</p>
</abstract>
</abstractGroup>
</contentMeta>
<noteGroup>
<note xml:id="fn1">
<p>A videotape accompanies this article.</p>
</note>
</noteGroup>
</header>
</component>
</istex:document>
</istex:metadataXml>
<mods version="3.6">
<titleInfo lang="en">
<title>SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report</title>
</titleInfo>
<titleInfo type="abbreviated" lang="en">
<title>Clinical/Scientific Notes</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en">
<title>SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report</title>
</titleInfo>
<name type="personal">
<namePart type="given">Alastair</namePart>
<namePart type="family">Wilkins</namePart>
<namePart type="termsOfAddress">PhD, MRCP</namePart>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Jerry M.</namePart>
<namePart type="family">Brown</namePart>
<namePart type="termsOfAddress">MD, MRCP</namePart>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Roger A.</namePart>
<namePart type="family">Barker</namePart>
<namePart type="termsOfAddress">PhD, MRCP</namePart>
<affiliation>Department of Neurology, Addenbrooke's Hospital, Cambridge, United Kingdom</affiliation>
<affiliation>E-mail: rab46@cus.cam.ac.uk</affiliation>
<affiliation>Correspondence address: Department of Neurology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre type="brief-communication" displayLabel="shortCommunication" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-S9SX2MFS-0">brief-communication</genre>
<originInfo>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place>
<placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2004-05</dateIssued>
<dateCaptured encoding="w3cdtf">2003-07-06</dateCaptured>
<dateValid encoding="w3cdtf">2003-10-21</dateValid>
<copyrightDate encoding="w3cdtf">2004</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription>
<extent unit="figures">0</extent>
<extent unit="tables">0</extent>
<extent unit="references">8</extent>
<extent unit="words">1192</extent>
</physicalDescription>
<abstract lang="en">We report on a young woman from the United Kingdom with L‐dopa–responsive parkinsonism with a trinucleotide repeat expansion in her spinocerebellar ataxia 2 (SCA2) gene. The case further extends the phenotype of SCA2 and emphasizes the importance of SCA screening in young‐onset parkinsonism, irrespective of ethnic origin. © 2004 Movement Disorder Society</abstract>
<note type="content">*A videotape accompanies this article.</note>
<subject lang="en">
<genre>keywords</genre>
<topic>SCA2</topic>
<topic>parkinsonism</topic>
<topic>levodopa</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre>
<note type="content"> This article contains supplementary video clips, available online at http://www.interscience.wiley.com/jpages/0885‐3185/suppmatSupporting Info Item: Supporting Information file suppmat_593.mpg - </note>
<subject>
<genre>article-category</genre>
<topic>Clinical/Scientific Note with Video</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2004</date>
<detail type="volume">
<caption>vol.</caption>
<number>19</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>5</number>
</detail>
<extent unit="pages">
<start>593</start>
<end>595</end>
<total>2</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">60163DD9E3887A992F60E772EFEFFCCE890DA0E7</identifier>
<identifier type="ark">ark:/67375/WNG-HCNJDV2R-1</identifier>
<identifier type="DOI">10.1002/mds.10715</identifier>
<identifier type="ArticleID">MDS10715</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 Movement Disorder Society</accessCondition>
<recordInfo>
<recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource>
<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
</recordInfo>
</mods>
<json:item>
<extension>json</extension>
<original>false</original>
<mimetype>application/json</mimetype>
<uri>https://api.istex.fr/document/60163DD9E3887A992F60E772EFEFFCCE890DA0E7/metadata/json</uri>
</json:item>
</metadata>
<serie></serie>
</istex>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/EdenteV2/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002F17 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 002F17 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    EdenteV2
   |flux=    Istex
   |étape=   Corpus
   |type=    RBID
   |clé=     ISTEX:60163DD9E3887A992F60E772EFEFFCCE890DA0E7
   |texte=   SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report
}}

Wicri

This area was generated with Dilib version V0.6.32.
Data generation: Thu Nov 30 15:26:48 2017. Site generation: Tue Mar 8 16:36:20 2022