Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study
Identifieur interne : 001104 ( Istex/Corpus ); précédent : 001103; suivant : 001105Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study
Auteurs : Klaus Seppi ; Michael F. H. Schocke ; Kathrin Prennschuetz-Schuetzenau ; Katherina J. Mair ; Regina Esterhammer ; Christian Kremser ; Armin Muigg ; Christoph Scherfler ; Werner Jaschke ; Gregor K. Wenning ; Werner PoeweSource :
- Movement Disorders [ 0885-3185 ] ; 2006-06-06.
English descriptors
Abstract
There is neuropathologic evidence that, in early stages of the Parkinson variant of multiple system atrophy (MSA‐P), the putamen shows a distinct topographical pathology affecting predominantly the dorsolateral and caudal regions while leaving the rostral to midparts almost intact. We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. Our study demonstrates prominent involvement of the posterior putamen in early disease stages of MSA‐P in vivo by assessing putaminal diffusivity with the help of DWI. © 2006 Movement Disorder Society
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DOI: 10.1002/mds.20843
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We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. Our study demonstrates prominent involvement of the posterior putamen in early disease stages of MSA‐P in vivo by assessing putaminal diffusivity with the help of DWI. © 2006 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Klaus Seppi MD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Michael F.H. Schocke MD</name><affiliations><json:string>Department of Radiology 1, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Kathrin Prennschuetz‐Schuetzenau PhD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Katherina J. Mair MD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Regina Esterhammer MD</name><affiliations><json:string>Department of Radiology 1, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Christian Kremser PhD</name><affiliations><json:string>Department of Radiology 1, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Armin Muigg MD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Christoph Scherfler MD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Werner Jaschke MD</name><affiliations><json:string>Department of Radiology 1, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Gregor K. Wenning MD, PhD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item><json:item><name>Werner Poewe MD</name><affiliations><json:string>Department of Neurology, Innsbruck Medical University, Austria</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>multiple system atrophy</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>putamen</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>magnetic resonance imaging</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>diffusion‐weighted imaging</value></json:item></subject><language><json:string>eng</json:string></language><abstract>There is neuropathologic evidence that, in early stages of the Parkinson variant of multiple system atrophy (MSA‐P), the putamen shows a distinct topographical pathology affecting predominantly the dorsolateral and caudal regions while leaving the rostral to midparts almost intact. We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. Our study demonstrates prominent involvement of the posterior putamen in early disease stages of MSA‐P in vivo by assessing putaminal diffusivity with the help of DWI. © 2006 Movement Disorder Society</abstract><qualityIndicators><score>6.577</score><pdfVersion>1.3</pdfVersion><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>1393</abstractCharCount><pdfWordCount>4081</pdfWordCount><pdfCharCount>25800</pdfCharCount><pdfPageCount>6</pdfPageCount><abstractWordCount>208</abstractWordCount></qualityIndicators><title>Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title><genre><json:string>Serial article</json:string></genre><host><volume>21</volume><pages><total>6</total><last>852</last><first>847</first></pages><issn><json:string>0885-3185</json:string></issn><issue>6</issue><subject><json:item><value>Brief Report</value></json:item></subject><genre></genre><language><json:string>unknown</json:string></language><title>Movement Disorders</title><doi><json:string>10.1002/(ISSN)1531-8257</json:string></doi></host><publicationDate>2006</publicationDate><copyrightDate>2006</copyrightDate><doi><json:string>10.1002/mds.20843</json:string></doi><id>B95B6BF7FBA7BB52A3621EBC0D17A3DF0B6A08D4</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/B95B6BF7FBA7BB52A3621EBC0D17A3DF0B6A08D4/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/B95B6BF7FBA7BB52A3621EBC0D17A3DF0B6A08D4/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/B95B6BF7FBA7BB52A3621EBC0D17A3DF0B6A08D4/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><p>Wiley Subscription Services, Inc., A Wiley Company</p></availability><date>2006</date></publicationStmt><notesStmt><note>Austrian Federal Ministry of Science and Transport - No. GZ 70038/2 PR 4/98;</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title><author><persName><forename type="first">Klaus</forename><surname>Seppi</surname><roleName type="degree">MD</roleName></persName><note type="biography">Drs. Seppi and Schocke contributed equally to this work.</note><affiliation>Drs. Seppi and Schocke contributed equally to this work.</affiliation><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Michael F.H.</forename><surname>Schocke</surname><roleName type="degree">MD</roleName></persName><note type="biography">Drs. Seppi and Schocke contributed equally to this work.</note><affiliation>Drs. Seppi and Schocke contributed equally to this work.</affiliation><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Kathrin</forename><surname>Prennschuetz‐Schuetzenau</surname><roleName type="degree">PhD</roleName></persName><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Katherina J.</forename><surname>Mair</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Regina</forename><surname>Esterhammer</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Christian</forename><surname>Kremser</surname><roleName type="degree">PhD</roleName></persName><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Armin</forename><surname>Muigg</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Christoph</forename><surname>Scherfler</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Werner</forename><surname>Jaschke</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Gregor K.</forename><surname>Wenning</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author><author><persName><forename type="first">Werner</forename><surname>Poewe</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Department of Neurology, Innsbruck Medical University, Innsbruck, Austria</p></note><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation></author></analytic><monogr><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. 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We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. 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number="2"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="29"></count><count type="wordTotal" number="4348"></count></countGroup><titleGroup><title type="main" xml:lang="en">Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title><title type="short" xml:lang="en">Topography of Putaminal Degeneration in MSA</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" noteRef="#fn1"><personName><givenNames>Klaus</givenNames><familyName>Seppi</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2" noteRef="#fn1"><personName><givenNames>Michael F.H.</givenNames><familyName>Schocke</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Kathrin</givenNames><familyName>Prennschuetz‐Schuetzenau</familyName><degrees>PhD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Katherina J.</givenNames><familyName>Mair</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Regina</givenNames><familyName>Esterhammer</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Christian</givenNames><familyName>Kremser</familyName><degrees>PhD</degrees></personName></creator><creator xml:id="au7" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Armin</givenNames><familyName>Muigg</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au8" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Christoph</givenNames><familyName>Scherfler</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au9" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Werner</givenNames><familyName>Jaschke</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au10" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Gregor K.</givenNames><familyName>Wenning</familyName><degrees>MD, PhD</degrees></personName></creator><creator xml:id="au11" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Werner</givenNames><familyName>Poewe</familyName><degrees>MD</degrees></personName><contactDetails><email>werner.poewe@uibk.ac.at</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="AT" type="organization"><unparsedAffiliation>Department of Neurology, Innsbruck Medical University, Austria</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="AT" type="organization"><unparsedAffiliation>Department of Radiology 1, Innsbruck Medical University, Austria</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">multiple system atrophy</keyword><keyword xml:id="kwd2">putamen</keyword><keyword xml:id="kwd3">magnetic resonance imaging</keyword><keyword xml:id="kwd4">diffusion‐weighted imaging</keyword></keywordGroup><fundingInfo><fundingAgency>Austrian Federal Ministry of Science and Transport</fundingAgency><fundingNumber>GZ 70038/2 PR 4/98</fundingNumber></fundingInfo><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>There is neuropathologic evidence that, in early stages of the Parkinson variant of multiple system atrophy (MSA‐P), the putamen shows a distinct topographical pathology affecting predominantly the dorsolateral and caudal regions while leaving the rostral to midparts almost intact. We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. Our study demonstrates prominent involvement of the posterior putamen in early disease stages of MSA‐P in vivo by assessing putaminal diffusivity with the help of DWI. © 2006 Movement Disorder Society</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p>Drs. Seppi and Schocke contributed equally to this work.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Topography of Putaminal Degeneration in MSA</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Topography of putaminal degeneration in multiple system atrophy: A diffusion magnetic resonance study</title></titleInfo><name type="personal"><namePart type="given">Klaus</namePart><namePart type="family">Seppi</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><description>Drs. Seppi and Schocke contributed equally to this work.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Michael F.H.</namePart><namePart type="family">Schocke</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation><description>Drs. Seppi and Schocke contributed equally to this work.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kathrin</namePart><namePart type="family">Prennschuetz‐Schuetzenau</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Katherina J.</namePart><namePart type="family">Mair</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Regina</namePart><namePart type="family">Esterhammer</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christian</namePart><namePart type="family">Kremser</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Armin</namePart><namePart type="family">Muigg</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christoph</namePart><namePart type="family">Scherfler</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Werner</namePart><namePart type="family">Jaschke</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Radiology 1, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Gregor K.</namePart><namePart type="family">Wenning</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Werner</namePart><namePart type="family">Poewe</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Innsbruck Medical University, Austria</affiliation><description>Correspondence: Department of Neurology, Innsbruck Medical University, Innsbruck, Austria</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">article</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2006-06-06</dateIssued><dateCaptured encoding="w3cdtf">2005-02-18</dateCaptured><dateValid encoding="w3cdtf">2005-10-04</dateValid><copyrightDate encoding="w3cdtf">2006</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">2</extent><extent unit="tables">1</extent><extent unit="references">29</extent><extent unit="words">4348</extent></physicalDescription><abstract lang="en">There is neuropathologic evidence that, in early stages of the Parkinson variant of multiple system atrophy (MSA‐P), the putamen shows a distinct topographical pathology affecting predominantly the dorsolateral and caudal regions while leaving the rostral to midparts almost intact. We investigated the topographic profile of putaminal degeneration in MSA‐P patients in vivo by means of diffusion‐weighted imaging (DWI), which has been shown to reveal abnormalities in the basal ganglia of patients with MSA‐P compared to patients with PD and healthy controls. For this purpose, regional trace of the diffusion tensor (rTrace(D)) values were determined in the entire, anterior, and posterior putamen in 15 patients with probable MSA‐P, in 20 patients with PD, and in 11 healthy volunteers matched for age and disease duration. MSA‐P patients had significantly higher rTrace(D) values in entire, anterior, and posterior putamen compared to both controls and PD patients. Trace(D) values were significantly higher in the posterior compared to the anterior putamen in the MSA‐P group. There were no significant differences between posterior and anterior putamen in both the control and PD group. Our study demonstrates prominent involvement of the posterior putamen in early disease stages of MSA‐P in vivo by assessing putaminal diffusivity with the help of DWI. © 2006 Movement Disorder Society</abstract><note type="funding">Austrian Federal Ministry of Science and Transport - No. GZ 70038/2 PR 4/98; </note><subject lang="en"><genre>Keywords</genre><topic>multiple system atrophy</topic><topic>putamen</topic><topic>magnetic resonance imaging</topic><topic>diffusion‐weighted imaging</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Brief Report</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>2006</date><detail type="volume"><caption>vol.</caption><number>21</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>847</start><end>852</end><total>6</total></extent></part></relatedItem><identifier type="istex">B95B6BF7FBA7BB52A3621EBC0D17A3DF0B6A08D4</identifier><identifier type="DOI">10.1002/mds.20843</identifier><identifier type="ArticleID">MDS20843</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2006 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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