Partial lesion of thalamic ventral intermediate nucleus after chronic high‐frequency stimulation
Identifieur interne : 002161 ( Istex/Corpus ); précédent : 002160; suivant : 002162Partial lesion of thalamic ventral intermediate nucleus after chronic high‐frequency stimulation
Auteurs : Jasmine Henderson ; Michael Rodriguez ; Dudley O'Sullivan ; Malcolm Pell ; Victor Fung ; Alim Louis Benabid ; Glenda HallidaySource :
- Movement Disorders [ 0885-3185 ] ; 2004-06.
English descriptors
- KwdEn :
- Benabid, Brain stimulation, Cannabis, Cell loss, Chronic stimulation, Deep brain stimulation, Disord, Electrode, Electrode track, Electrode tract, Gliosis, Halliday, Lewy, Lewy bodies, Mild gliosis, Movement disorders, Myoclonus, Neurol, Neurology, Neuron, Neuronal, Neuronal loss, Propriospinal, Propriospinal myoclonus, Pulse width, Spinal, Substantia nigra, Thalamic, Thalamic nucleus, Thalamic stimulation, Tremor, Tremor improvement, Unmedicated state, Unoperated side, Upper limb, Ventral, Years postoperatively.
- Teeft :
- Benabid, Brain stimulation, Cannabis, Cell loss, Chronic stimulation, Deep brain stimulation, Disord, Electrode, Electrode track, Electrode tract, Gliosis, Halliday, Lewy, Lewy bodies, Mild gliosis, Movement disorders, Myoclonus, Neurol, Neurology, Neuron, Neuronal, Neuronal loss, Propriospinal, Propriospinal myoclonus, Pulse width, Spinal, Substantia nigra, Thalamic, Thalamic nucleus, Thalamic stimulation, Tremor, Tremor improvement, Unmedicated state, Unoperated side, Upper limb, Ventral, Years postoperatively.
Abstract
A 73‐year‐old man with Parkinson's disease underwent thalamic stimulation for disabling tremor with excellent results only when stimulation on. Post‐mortem neuropathology (7 years postoperatively) revealed 60% cell loss within 0.5 mm of the electrode tip. Tremor improvement was attributable to chronic stimulation, not microthalamotomy. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.10709
Links to Exploration step
ISTEX:B0737E8230CBACD2E45D8DE0BBCE0F77E70F0642Le document en format XML
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Australia</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">6</biblScope><biblScope unit="page" from="709">709</biblScope><biblScope unit="page" to="711">711</biblScope><biblScope unit="page-count">3</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2004-06">2004-06</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>Benabid</term><term>Brain stimulation</term><term>Cannabis</term><term>Cell loss</term><term>Chronic stimulation</term><term>Deep brain stimulation</term><term>Disord</term><term>Electrode</term><term>Electrode track</term><term>Electrode tract</term><term>Gliosis</term><term>Halliday</term><term>Lewy</term><term>Lewy bodies</term><term>Mild gliosis</term><term>Movement disorders</term><term>Myoclonus</term><term>Neurol</term><term>Neurology</term><term>Neuron</term><term>Neuronal</term><term>Neuronal loss</term><term>Propriospinal</term><term>Propriospinal myoclonus</term><term>Pulse width</term><term>Spinal</term><term>Substantia nigra</term><term>Thalamic</term><term>Thalamic nucleus</term><term>Thalamic stimulation</term><term>Tremor</term><term>Tremor improvement</term><term>Unmedicated state</term><term>Unoperated side</term><term>Upper limb</term><term>Ventral</term><term>Years postoperatively</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Benabid</term><term>Brain stimulation</term><term>Cannabis</term><term>Cell loss</term><term>Chronic stimulation</term><term>Deep brain 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when stimulation on. Post‐mortem neuropathology (7 years postoperatively) revealed 60% cell loss within 0.5 mm of the electrode tip. 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role="corresp"><persName><forename type="first">Jasmine</forename><surname>Henderson</surname><roleName type="degree">PhD</roleName></persName><email>jasmine@med.usyd.edu.au</email><affiliation>Department of Pharmacology, University of Sydney, Sydney, Australia<address><country key="AU"></country></address></affiliation><affiliation>Prince of Wales Medical Research Institute, Randwick, Australia<address><country key="AU"></country></address></affiliation><affiliation>University of New South Wales, Kensington, Australia<address><country key="AU"></country></address></affiliation><affiliation>Department of Pharmacology, Room 211e, Bosch Building, University of Sydney, NSW 2006, Australia</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Michael</forename><surname>Rodriguez</surname><roleName type="degree">FRCPA</roleName></persName><affiliation>Department of Forensic Medicine, Central Sydney Area Health Service, Glebe, Australia<address><country 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type="published" when="2004-06"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>A 73‐year‐old man with Parkinson's disease underwent thalamic stimulation for disabling tremor with excellent results only when stimulation <hi rend="italic">on</hi>. Post‐mortem neuropathology (7 years postoperatively) revealed 60% cell loss within 0.5 mm of the electrode tip. Tremor improvement was attributable to chronic stimulation, not microthalamotomy. © 2004 Movement Disorder Society</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">VIM stimulation</term><term xml:id="kwd2">Parkinson's disease</term></keywords><keywords rend="articleCategory"><term>Clinical/Scientific Note</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/B0737E8230CBACD2E45D8DE0BBCE0F77E70F0642/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="60"><doi origin="wiley" registered="yes">10.1002/mds.v19:6</doi><numberingGroup><numbering type="journalVolume" number="19">19</numbering><numbering type="journalIssue">6</numbering></numberingGroup><coverDate startDate="2004-06">June 2004</coverDate></publicationMeta><publicationMeta level="unit" type="shortCommunication" position="190" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.10709</doi><idGroup><id type="unit" value="MDS10709"></id></idGroup><countGroup><count type="pageTotal" number="3"></count></countGroup><titleGroup><title type="articleCategory">Clinical/Scientific Note</title><title type="tocHeading1">Clinical/Scientific Notes</title></titleGroup><copyright ownership="thirdParty">Copyright © 2004 Movement Disorder Society</copyright><eventGroup><event type="manuscriptReceived" date="2003-06-12"></event><event type="manuscriptRevised" date="2003-09-15"></event><event type="manuscriptAccepted" date="2003-10-15"></event><event type="publishedOnlineEarlyUnpaginated" date="2004-01-29"></event><event type="firstOnline" date="2004-01-29"></event><event type="publishedOnlineFinalForm" date="2004-06-03"></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">709</numbering><numbering type="pageLast">711</numbering></numberingGroup><correspondenceTo>Department of Pharmacology, Room 211e, Bosch Building, University of Sydney, NSW 2006, Australia</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS10709.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="1"></count><count type="tableTotal" number="0"></count><count type="referenceTotal" number="12"></count><count type="wordTotal" number="1974"></count></countGroup><titleGroup><title type="main" xml:lang="en">Partial lesion of thalamic ventral intermediate nucleus after chronic high‐frequency stimulation</title><title type="short" xml:lang="en">Clinical/Scientific Notes</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1 #af2 #af3" corresponding="yes"><personName><givenNames>Jasmine</givenNames><familyName>Henderson</familyName><degrees>PhD</degrees></personName><contactDetails><email>jasmine@med.usyd.edu.au</email></contactDetails></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af4"><personName><givenNames>Michael</givenNames><familyName>Rodriguez</familyName><degrees>FRCPA</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af5"><personName><givenNames>Dudley</givenNames><familyName>O'Sullivan</familyName><degrees>FRACP</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af5"><personName><givenNames>Malcolm</givenNames><familyName>Pell</familyName><degrees>FRACS</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af6"><personName><givenNames>Victor</givenNames><familyName>Fung</familyName><degrees>PhD, FRACP</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af5 #af7"><personName><givenNames>Alim Louis</givenNames><familyName>Benabid</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au7" creatorRole="author" affiliationRef="#af2 #af3"><personName><givenNames>Glenda</givenNames><familyName>Halliday</familyName><degrees>PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="AU" type="organization"><unparsedAffiliation>Department of Pharmacology, University of Sydney, Sydney, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="AU" type="organization"><unparsedAffiliation>Prince of Wales Medical Research Institute, Randwick, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="AU" type="organization"><unparsedAffiliation>University of New South Wales, Kensington, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="AU" type="organization"><unparsedAffiliation>Department of Forensic Medicine, Central Sydney Area Health Service, Glebe, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="AU" type="organization"><unparsedAffiliation>Departments of Neurology and Neurosurgery, St. Vincent's Hospital, South Eastern Sydney Area Health Service, Darlinghurst, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af6" countryCode="AU" type="organization"><unparsedAffiliation>Department of Neurology, Westmead Hospital, Westmead, Australia</unparsedAffiliation></affiliation><affiliation xml:id="af7" countryCode="FR" type="organization"><unparsedAffiliation>Neurosciences Department, Joseph Fourier University, Centre Hospitalier Universitaire, Grenoble, France</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">VIM stimulation</keyword><keyword xml:id="kwd2">Parkinson's disease</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>A 73‐year‐old man with Parkinson's disease underwent thalamic stimulation for disabling tremor with excellent results only when stimulation <i>on</i>. Post‐mortem neuropathology (7 years postoperatively) revealed 60% cell loss within 0.5 mm of the electrode tip. Tremor improvement was attributable to chronic stimulation, not microthalamotomy. © 2004 Movement Disorder Society</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Partial lesion of thalamic ventral intermediate nucleus after chronic high‐frequency stimulation</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Partial lesion of thalamic ventral intermediate nucleus after chronic high‐frequency stimulation</title></titleInfo><name type="personal"><namePart type="given">Jasmine</namePart><namePart type="family">Henderson</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Department of Pharmacology, University of Sydney, Sydney, Australia</affiliation><affiliation>Prince of Wales Medical Research Institute, Randwick, Australia</affiliation><affiliation>University of New South Wales, Kensington, Australia</affiliation><affiliation>E-mail: jasmine@med.usyd.edu.au</affiliation><affiliation>Correspondence address: Department of Pharmacology, Room 211e, Bosch Building, University of Sydney, NSW 2006, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Michael</namePart><namePart type="family">Rodriguez</namePart><namePart type="termsOfAddress">FRCPA</namePart><affiliation>Department of Forensic Medicine, Central Sydney Area Health Service, Glebe, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Dudley</namePart><namePart type="family">O'Sullivan</namePart><namePart type="termsOfAddress">FRACP</namePart><affiliation>Departments of Neurology and Neurosurgery, St. Vincent's Hospital, South Eastern Sydney Area Health Service, Darlinghurst, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Malcolm</namePart><namePart type="family">Pell</namePart><namePart type="termsOfAddress">FRACS</namePart><affiliation>Departments of Neurology and Neurosurgery, St. Vincent's Hospital, South Eastern Sydney Area Health Service, Darlinghurst, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Victor</namePart><namePart type="family">Fung</namePart><namePart type="termsOfAddress">PhD, FRACP</namePart><affiliation>Department of Neurology, Westmead Hospital, Westmead, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alim Louis</namePart><namePart type="family">Benabid</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Departments of Neurology and Neurosurgery, St. Vincent's Hospital, South Eastern Sydney Area Health Service, Darlinghurst, Australia</affiliation><affiliation>Neurosciences Department, Joseph Fourier University, Centre Hospitalier Universitaire, Grenoble, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Glenda</namePart><namePart type="family">Halliday</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Prince of Wales Medical Research Institute, Randwick, Australia</affiliation><affiliation>University of New South Wales, Kensington, Australia</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">2004-06</dateIssued><dateCaptured encoding="w3cdtf">2003-06-12</dateCaptured><dateValid encoding="w3cdtf">2003-10-15</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">1</extent><extent unit="tables">0</extent><extent unit="references">12</extent><extent unit="words">1974</extent></physicalDescription><abstract lang="en">A 73‐year‐old man with Parkinson's disease underwent thalamic stimulation for disabling tremor with excellent results only when stimulation on. Post‐mortem neuropathology (7 years postoperatively) revealed 60% cell loss within 0.5 mm of the electrode tip. Tremor improvement was attributable to chronic stimulation, not microthalamotomy. © 2004 Movement Disorder Society</abstract><subject lang="en"><genre>keywords</genre><topic>VIM stimulation</topic><topic>Parkinson's disease</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. 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