Clinical variants of idiopathic torsion dystonia.
Identifieur interne : 000B18 ( Istex/Curation ); précédent : 000B17; suivant : 000B19Clinical variants of idiopathic torsion dystonia.
Auteurs : S. FahnSource :
- Journal of Neurology, Neurosurgery & Psychiatry [ 0022-3050 ] ; 1989-06.
Abstract
Some patients with dystonic movements and postures not known to be caused by environmental or degenerative disorders can be segregated from classical-appearing idiopathic torsion dystonia on the basis of distinctive clinical and pharmacologic features. Many of them should be considered within the family of dystonia, as clinical variants of idiopathic torsion dystonia, while others are better classified as being part of other families of dyskinesias. In the former group are paradoxical dystonia, myoclonic dystonia, diurnal dystonia, and dopa-responsive dystonia. The latter group consists of dystonic tics and the various entities comprising paroxysmal dystonia, namely kinesigenic, nonkinesigenic and hypnogenic dystonia.
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DOI: 10.1136/jnnp.52.Suppl.96
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S. Fahn<affiliation><mods:affiliation>Department of Neurology, Columbia University College of Physicians & Surgeons, New York.</mods:affiliation><wicri:noCountry code="subField">New York.</wicri:noCountry></affiliation>Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Clinical variants of idiopathic torsion dystonia.</title><author wicri:is="90%"><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S" last="Fahn">S. Fahn</name><affiliation><mods:affiliation>Department of Neurology, Columbia University College of Physicians & Surgeons, New York.</mods:affiliation><wicri:noCountry code="subField">New York.</wicri:noCountry></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:DD79FAA275B66357CC83A4C1B502513FA709A405</idno><date when="1989-06-01" year="1989">1989-06-01</date><idno type="doi">10.1136/jnnp.52.Suppl.96</idno><idno type="url">https://api.istex.fr/document/DD79FAA275B66357CC83A4C1B502513FA709A405/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000B18</idno><idno type="wicri:Area/Istex/Curation">000B18</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Clinical variants of idiopathic torsion dystonia.</title><author wicri:is="90%"><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S" last="Fahn">S. Fahn</name><affiliation><mods:affiliation>Department of Neurology, Columbia University College of Physicians & Surgeons, New York.</mods:affiliation><wicri:noCountry code="subField">New York.</wicri:noCountry></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of Neurology, Neurosurgery & Psychiatry</title><title level="j" type="abbrev">J Neurol Neurosurg Psychiatry</title><idno type="ISSN">0022-3050</idno><idno type="eISSN">1468-330X</idno><imprint><publisher>BMJ Publishing Group Ltd</publisher><date type="published" when="1989-06">1989-06</date><biblScope unit="volume">52</biblScope><biblScope unit="issue">Suppl</biblScope><biblScope unit="page" from="96">96</biblScope></imprint><idno type="ISSN">0022-3050</idno></series><idno type="istex">DD79FAA275B66357CC83A4C1B502513FA709A405</idno><idno type="DOI">10.1136/jnnp.52.Suppl.96</idno><idno type="href">jnnp-52-96.pdf</idno><idno type="PMID">2666583</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0022-3050</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Some patients with dystonic movements and postures not known to be caused by environmental or degenerative disorders can be segregated from classical-appearing idiopathic torsion dystonia on the basis of distinctive clinical and pharmacologic features. Many of them should be considered within the family of dystonia, as clinical variants of idiopathic torsion dystonia, while others are better classified as being part of other families of dyskinesias. In the former group are paradoxical dystonia, myoclonic dystonia, diurnal dystonia, and dopa-responsive dystonia. The latter group consists of dystonic tics and the various entities comprising paroxysmal dystonia, namely kinesigenic, nonkinesigenic and hypnogenic dystonia.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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