Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977
Identifieur interne : 000F16 ( Istex/Corpus ); précédent : 000F15; suivant : 000F17Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977
Auteurs : Ph Brown ; Françoise Cathala ; Doris Sadowsky ; D. C. GajdusekSource :
- Annals of Neurology [ 0364-5134 ] ; 1979-11.
Abstract
One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.
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DOI: 10.1002/ana.410060510
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Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title><author><name sortKey="Brown, Ph" sort="Brown, Ph" uniqKey="Brown P" first="Ph" last="Brown">Ph Brown</name><affiliation><mods:affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation><affiliation><mods:affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation><affiliation><mods:affiliation>Bldg 36, Room 5B25, NINCDS, NIH, Bethesda, MD 20014</mods:affiliation></affiliation></author><author><name sortKey="Cathala, Francoise" sort="Cathala, Francoise" uniqKey="Cathala F" first="Françoise" last="Cathala">Françoise Cathala</name><affiliation><mods:affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation><affiliation><mods:affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation></author><author><name sortKey="Sadowsky, Doris" sort="Sadowsky, Doris" uniqKey="Sadowsky D" first="Doris" last="Sadowsky">Doris Sadowsky</name><affiliation><mods:affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation><affiliation><mods:affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation></author><author><name sortKey="Gajdusek, D C" sort="Gajdusek, D C" uniqKey="Gajdusek D" first="D. C." last="Gajdusek">D. C. Gajdusek</name><affiliation><mods:affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation><affiliation><mods:affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Annals of Neurology</title><title level="j" type="sub">Official Journal of the American Neurological Association and the Child Neurology Society</title><title level="j" type="abbrev">Ann Neurol.</title><idno type="ISSN">0364-5134</idno><idno type="eISSN">1531-8249</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1979-11">1979-11</date><biblScope unit="volume">6</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="430">430</biblScope><biblScope unit="page" to="437">437</biblScope></imprint><idno type="ISSN">0364-5134</idno></series><idno type="istex">D3CD8DFDEB297BD3EF4EBBBF72FD98671A9F3EE7</idno><idno type="DOI">10.1002/ana.410060510</idno><idno type="ArticleID">ANA410060510</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0364-5134</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Dr Brown MD</name><affiliations><json:string>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</json:string><json:string>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</json:string><json:string>Bldg 36, Room 5B25, NINCDS, NIH, Bethesda, MD 20014</json:string></affiliations></json:item><json:item><name>Françoise Cathala MD</name><affiliations><json:string>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</json:string><json:string>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</json:string></affiliations></json:item><json:item><name>Doris Sadowsky</name><affiliations><json:string>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</json:string><json:string>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</json:string></affiliations></json:item><json:item><name>D. C. Gajdusek MD</name><affiliations><json:string>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</json:string><json:string>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</json:string></affiliations></json:item></author><articleId><json:string>ANA410060510</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.</abstract><qualityIndicators><score>6.06</score><pdfVersion>1.3</pdfVersion><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>925</abstractCharCount><pdfWordCount>4320</pdfWordCount><pdfCharCount>27265</pdfCharCount><pdfPageCount>8</pdfPageCount><abstractWordCount>145</abstractWordCount></qualityIndicators><title>Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title><refBibs><json:item><author><json:item><name>C Bernoulli</name></json:item><json:item><name>C Masters</name></json:item><json:item><name>DC Gajdusek</name></json:item></author><host><volume>1</volume><pages><last>252</last><first>229</first></pages><author></author><title>Slow Transmissible Diseases of the Nervous System</title></host><title>The early clinical features of Creutzfeldt‐Jakob disease (subacute spongiform encephalopathy)</title></json:item><json:item><author><json:item><name>M Bonduelle</name></json:item><json:item><name>R Escourolle</name></json:item><json:item><name>P Bouyques</name></json:item></author><host><volume>125</volume><pages><last>209</last><first>197</first></pages><author></author><title>Rev Neurol (Paris)</title></host><title>Maladie de Creutzfeldt‐Jakob familiale Observation anatomo‐clinique</title></json:item><json:item><author><json:item><name>P Brown</name></json:item><json:item><name>F Cathala</name></json:item></author><host><volume>5</volume><pages><last>192</last><first>189</first></pages><author></author><title>Ann Neurol</title></host><title>Creutzfeldt‐Jakob disease in France: I. 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Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><p>Copyright © 1979 American Neurological Association</p></availability><date>1979</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title><author xml:id="author-1"><persName><surname>Brown</surname></persName><roleName type="degree">Dr</roleName><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>Bldg 36, Room 5B25, NINCDS, NIH, Bethesda, MD 20014</affiliation></author><author xml:id="author-2"><persName><forename type="first">Françoise</forename><surname>Cathala</surname></persName><roleName type="degree">MD</roleName><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation></author><author xml:id="author-3"><persName><forename type="first">Doris</forename><surname>Sadowsky</surname></persName><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation></author><author xml:id="author-4"><persName><forename type="first">D. C.</forename><surname>Gajdusek</surname></persName><roleName type="degree">MD</roleName><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation></author></analytic><monogr><title level="j">Annals of Neurology</title><title level="j" type="sub">Official Journal of the American Neurological Association and the Child Neurology Society</title><title level="j" type="abbrev">Ann Neurol.</title><idno type="pISSN">0364-5134</idno><idno type="eISSN">1531-8249</idno><idno type="DOI">10.1002/(ISSN)1531-8249</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1979-11"></date><biblScope unit="volume">6</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="430">430</biblScope><biblScope unit="page" to="437">437</biblScope></imprint></monogr><idno type="istex">D3CD8DFDEB297BD3EF4EBBBF72FD98671A9F3EE7</idno><idno type="DOI">10.1002/ana.410060510</idno><idno type="ArticleID">ANA410060510</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1979</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>article-category</head><item><term>Article</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1979-04-15">Registration</change><change when="1979-11">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/D3CD8DFDEB297BD3EF4EBBBF72FD98671A9F3EE7/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)1531-8249</doi><issn type="print">0364-5134</issn><issn type="electronic">1531-8249</issn><idGroup><id type="product" value="ANA"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="ANNALS OF NEUROLOGY">Annals of Neurology</title><title type="subtitle">Official Journal of the American Neurological Association and the Child Neurology Society</title><title type="short">Ann Neurol.</title></titleGroup></publicationMeta><publicationMeta level="part" position="50"><doi origin="wiley" registered="yes">10.1002/ana.v6:5</doi><numberingGroup><numbering type="journalVolume" number="6">6</numbering><numbering type="journalIssue">5</numbering></numberingGroup><coverDate startDate="1979-11">November 1979</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="10" status="forIssue"><doi origin="wiley" registered="yes">10.1002/ana.410060510</doi><idGroup><id type="unit" value="ANA410060510"></id></idGroup><countGroup><count type="pageTotal" number="8"></count></countGroup><titleGroup><title type="articleCategory">Article</title><title type="tocHeading1">Articles</title></titleGroup><copyright ownership="thirdParty">Copyright © 1979 American Neurological Association</copyright><eventGroup><event type="manuscriptAccepted" date="1979-04-15"></event><event type="firstOnline" date="2004-10-07"></event><event type="publishedOnlineFinalForm" date="2004-10-07"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.1 mode:FullText source:HeaderRef result:HeaderRef" date="2010-02-23"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-03"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-14"></event></eventGroup><numberingGroup><numbering type="pageFirst">430</numbering><numbering type="pageLast">437</numbering></numberingGroup><correspondenceTo>Bldg 36, Room 5B25, NINCDS, NIH, Bethesda, MD 20014</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:ANA.ANA410060510.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="2"></count><count type="tableTotal" number="5"></count><count type="referenceTotal" number="17"></count></countGroup><titleGroup><title type="main" xml:lang="en">Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title><title type="short" xml:lang="en">Clinical Characteristics of CJD in France</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1 #af2" corresponding="yes"><personName><honorifics>Dr</honorifics><givenNames>Paul</givenNames><familyName>Brown</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1 #af2"><personName><givenNames>Françoise</givenNames><familyName>Cathala</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1 #af2"><personName><givenNames>Doris</givenNames><familyName>Sadowsky</familyName></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1 #af2"><personName><givenNames>D. C.</givenNames><familyName>Gajdusek</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="FR" type="organization"><unparsedAffiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="FR" type="organization"><unparsedAffiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical Characteristics of CJD in France</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Creutzfeldt‐Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968–1977</title></titleInfo><name type="personal"><namePart type="termsOfAddress">Dr</namePart><namePart type="family">Brown</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>Bldg 36, Room 5B25, NINCDS, NIH, Bethesda, MD 20014</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Françoise</namePart><namePart type="family">Cathala</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Doris</namePart><namePart type="family">Sadowsky</namePart><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D. C.</namePart><namePart type="family">Gajdusek</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Laboratory of Central Nervous System Studies and the Office of Biometry and Epidemiology, Hǒpital de la Salpětrière, Paris, France</affiliation><affiliation>NINCDS, NIH, and the Laboratoire de Neurovirologie, Hǒpital de la Salpětrière, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">1979-11</dateIssued><dateValid encoding="w3cdtf">1979-04-15</dateValid><copyrightDate encoding="w3cdtf">1979</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">5</extent><extent unit="references">17</extent></physicalDescription><abstract lang="en">One hundred twenty‐four consecutive cases of Creutzfeldt‐Jakob disease (CJD) in France, verified by biopsy or autopsy between 1968 and 1977, were analyzed with respect to their clinical characteristics. The series comprised equal numbers of men and women, with the most frequent age at onset being 60 to 64 years and the most frequent duration, two to three months. A prodromal illness was observed in more than one‐third of the patients. Clinical presentations and symptom frequencies are tabulated, and a multifactor analysis has been performed to obtain those combinations of symptoms and signs which occurred at least as often as the triad of dementia, myoclonus, and a positive electroencephalogram. Two groups of atypical cases are also emphasized: one with sudden, strokelike presentation and rapidly evolving illness of less than 2 moths' duration, and the other with a long clinical course of between 2 and 10 years.</abstract><relatedItem type="host"><titleInfo><title>Annals of Neurology</title><subTitle>Official Journal of the American Neurological Association and the Child Neurology Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>Ann Neurol.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Article</topic></subject><identifier type="ISSN">0364-5134</identifier><identifier type="eISSN">1531-8249</identifier><identifier type="DOI">10.1002/(ISSN)1531-8249</identifier><identifier type="PublisherID">ANA</identifier><part><date>1979</date><detail type="volume"><caption>vol.</caption><number>6</number></detail><detail type="issue"><caption>no.</caption><number>5</number></detail><extent unit="pages"><start>430</start><end>437</end><total>8</total></extent></part></relatedItem><identifier type="istex">D3CD8DFDEB297BD3EF4EBBBF72FD98671A9F3EE7</identifier><identifier type="DOI">10.1002/ana.410060510</identifier><identifier type="ArticleID">ANA410060510</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1979 American Neurological Association</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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