Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness

Abstract Background Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic congenital hearing loss. The contribution of congenital CMV to prelingual deafness and the pathophysiology is largely unknown. Objective (1) To analyze the prevalence of congenital CMV among cochlear i...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical virology 2013-02, Vol.56 (2), p.113-117
Hauptverfasser: de Vries, Jutte J.C, Vesseur, Annemarie, Rotteveel, Liselotte J.C, Korver, Anna M.H, Rusman, Lisette G, Wessels, Els, Kroes, Aloys C.M, Mylanus, Emmanuel A, Oudesluys-Murphy, Anne M, Frijns, Johan H.M, Vossen, Ann C.T.M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 117
container_issue 2
container_start_page 113
container_title Journal of clinical virology
container_volume 56
creator de Vries, Jutte J.C
Vesseur, Annemarie
Rotteveel, Liselotte J.C
Korver, Anna M.H
Rusman, Lisette G
Wessels, Els
Kroes, Aloys C.M
Mylanus, Emmanuel A
Oudesluys-Murphy, Anne M
Frijns, Johan H.M
Vossen, Ann C.T.M
description Abstract Background Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic congenital hearing loss. The contribution of congenital CMV to prelingual deafness and the pathophysiology is largely unknown. Objective (1) To analyze the prevalence of congenital CMV among cochlear implant (CI) recipients with prelingual deafness. (2) To genotype CMV present in dried blood spots (DBS) and in the inner ear years after birth. Study design Children and adults with prelingual deafness who received a CI in 2010–2011 were included prospectively. Perilymphatic fluids were collected during CI surgery and, in the pediatric cases, DBS were retrieved for CMV DNA detection. Furthermore, a cohort of children with prelingual deafness who received a CI between 2003 and 2008 were included retrospectively. CMV detection in DBS and perilymph was followed by gB and gH genotyping. Results Seventysix pediatric CI recipients were included. Seventy DBS were tested for CMV DNA, resulting in a prevalence of congenital CMV of 14% (10/70). Perilymphatic fluid was available from 29 pediatric CI recipients. One perilymph fluid, of a 21-month old girl with congenital CMV, asymptomatic at birth, was CMV DNA positive. The CMV strain in the perilymph was genotypically identical to the strain present in her DBS (gB1/gH2). Perilymph samples from 21 adult CI recipients were CMV DNA negative. Conclusions Our study stresses the important contribution of congenital CMV among pediatric CI recipients. Furthermore, our genotyping data support the hypothesis that CMV-related hearing loss is associated with ongoing viral replication in the inner ear up to years after birth.
doi_str_mv 10.1016/j.jcv.2012.10.008
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1273506711</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1386653212003897</els_id><sourcerecordid>1273506711</sourcerecordid><originalsourceid>FETCH-LOGICAL-c471t-36e6c9e0562b303934a8ccbd7808f92c4023b591d7ac6f5027bcca24d0d24cca3</originalsourceid><addsrcrecordid>eNqNks2KFDEQgBtR3HX1AbxILoKXHvPTnaQRhGX8hUUP6jmkk_ROxnSnTdIj8yi-rdXMqOBBPCWpfFUV6ktVPSZ4QzDhz_ebvTlsKCYUzhuM5Z3qkkjB6rbj4i7smeQ1bxm9qB7kvMeYtKwR96sLykhDOoYvqx_bY4mju9UhHnxaMnr14RpZV5wpPk7IT8gm7yzqQ4wW5TmWjPRk0eySD8dx3uniDRrC4m1GQ4oj3FivS4Loymm7hIJMNLvgdEJ-nIOeCkrO-Nm7Cap992WH5uSCn24XHaC5HiaX88Pq3qBDdo_O61X15c3rz9t39c3Ht--31ze1aQQpNeOOm87hltOeYdaxRktjeisklkNHTYMp69uOWKENH1pMRW-Mpo3FljawY1fVs1PdOcVvi8tFjT4bF-CdLi5ZESpYi7kg5H9QgBspKaDkhJoUc05uUHPyo05HRbBa5am9AnlqlbeGQB7kPDmXX_rR2d8Zv2wB8PQM6Gx0GJKejM9_OC4ZllwA9-LEOZjbwbuksoFhGzADgy_KRv_PZ7z8K9uAGw8Nv7qjy_u4pAmEKKIyVVh9Wn_Z-skIxZjJTrCfet_O6Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1272734882</pqid></control><display><type>article</type><title>Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>de Vries, Jutte J.C ; Vesseur, Annemarie ; Rotteveel, Liselotte J.C ; Korver, Anna M.H ; Rusman, Lisette G ; Wessels, Els ; Kroes, Aloys C.M ; Mylanus, Emmanuel A ; Oudesluys-Murphy, Anne M ; Frijns, Johan H.M ; Vossen, Ann C.T.M</creator><creatorcontrib>de Vries, Jutte J.C ; Vesseur, Annemarie ; Rotteveel, Liselotte J.C ; Korver, Anna M.H ; Rusman, Lisette G ; Wessels, Els ; Kroes, Aloys C.M ; Mylanus, Emmanuel A ; Oudesluys-Murphy, Anne M ; Frijns, Johan H.M ; Vossen, Ann C.T.M</creatorcontrib><description>Abstract Background Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic congenital hearing loss. The contribution of congenital CMV to prelingual deafness and the pathophysiology is largely unknown. Objective (1) To analyze the prevalence of congenital CMV among cochlear implant (CI) recipients with prelingual deafness. (2) To genotype CMV present in dried blood spots (DBS) and in the inner ear years after birth. Study design Children and adults with prelingual deafness who received a CI in 2010–2011 were included prospectively. Perilymphatic fluids were collected during CI surgery and, in the pediatric cases, DBS were retrieved for CMV DNA detection. Furthermore, a cohort of children with prelingual deafness who received a CI between 2003 and 2008 were included retrospectively. CMV detection in DBS and perilymph was followed by gB and gH genotyping. Results Seventysix pediatric CI recipients were included. Seventy DBS were tested for CMV DNA, resulting in a prevalence of congenital CMV of 14% (10/70). Perilymphatic fluid was available from 29 pediatric CI recipients. One perilymph fluid, of a 21-month old girl with congenital CMV, asymptomatic at birth, was CMV DNA positive. The CMV strain in the perilymph was genotypically identical to the strain present in her DBS (gB1/gH2). Perilymph samples from 21 adult CI recipients were CMV DNA negative. Conclusions Our study stresses the important contribution of congenital CMV among pediatric CI recipients. Furthermore, our genotyping data support the hypothesis that CMV-related hearing loss is associated with ongoing viral replication in the inner ear up to years after birth.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2012.10.008</identifier><identifier>PMID: 23141930</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Allergy and Immunology ; Biological and medical sciences ; Birth ; Blood - virology ; Child ; Child, Preschool ; Cochlear implant ; Cochlear Implants ; Congenital cytomegalovirus ; Cytomegalovirus ; Cytomegalovirus - classification ; Cytomegalovirus - genetics ; Cytomegalovirus - isolation &amp; purification ; Cytomegalovirus Infections - congenital ; Cytomegalovirus Infections - virology ; Deafness - etiology ; Deafness - virology ; Desiccation ; DNA, Viral - genetics ; DNA, Viral - isolation &amp; purification ; Female ; Fundamental and applied biological sciences. Psychology ; Genotype ; Human viral diseases ; Humans ; Infant ; Infant, Newborn ; Infectious Disease ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Middle Aged ; Miscellaneous ; Perilymph - virology ; Specimen Handling - methods ; Viral diseases ; Virology ; Young Adult</subject><ispartof>Journal of clinical virology, 2013-02, Vol.56 (2), p.113-117</ispartof><rights>Elsevier B.V.</rights><rights>2012 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-36e6c9e0562b303934a8ccbd7808f92c4023b591d7ac6f5027bcca24d0d24cca3</citedby><cites>FETCH-LOGICAL-c471t-36e6c9e0562b303934a8ccbd7808f92c4023b591d7ac6f5027bcca24d0d24cca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1386653212003897$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26830867$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23141930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Vries, Jutte J.C</creatorcontrib><creatorcontrib>Vesseur, Annemarie</creatorcontrib><creatorcontrib>Rotteveel, Liselotte J.C</creatorcontrib><creatorcontrib>Korver, Anna M.H</creatorcontrib><creatorcontrib>Rusman, Lisette G</creatorcontrib><creatorcontrib>Wessels, Els</creatorcontrib><creatorcontrib>Kroes, Aloys C.M</creatorcontrib><creatorcontrib>Mylanus, Emmanuel A</creatorcontrib><creatorcontrib>Oudesluys-Murphy, Anne M</creatorcontrib><creatorcontrib>Frijns, Johan H.M</creatorcontrib><creatorcontrib>Vossen, Ann C.T.M</creatorcontrib><title>Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness</title><title>Journal of clinical virology</title><addtitle>J Clin Virol</addtitle><description>Abstract Background Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic congenital hearing loss. The contribution of congenital CMV to prelingual deafness and the pathophysiology is largely unknown. Objective (1) To analyze the prevalence of congenital CMV among cochlear implant (CI) recipients with prelingual deafness. (2) To genotype CMV present in dried blood spots (DBS) and in the inner ear years after birth. Study design Children and adults with prelingual deafness who received a CI in 2010–2011 were included prospectively. Perilymphatic fluids were collected during CI surgery and, in the pediatric cases, DBS were retrieved for CMV DNA detection. Furthermore, a cohort of children with prelingual deafness who received a CI between 2003 and 2008 were included retrospectively. CMV detection in DBS and perilymph was followed by gB and gH genotyping. Results Seventysix pediatric CI recipients were included. Seventy DBS were tested for CMV DNA, resulting in a prevalence of congenital CMV of 14% (10/70). Perilymphatic fluid was available from 29 pediatric CI recipients. One perilymph fluid, of a 21-month old girl with congenital CMV, asymptomatic at birth, was CMV DNA positive. The CMV strain in the perilymph was genotypically identical to the strain present in her DBS (gB1/gH2). Perilymph samples from 21 adult CI recipients were CMV DNA negative. Conclusions Our study stresses the important contribution of congenital CMV among pediatric CI recipients. Furthermore, our genotyping data support the hypothesis that CMV-related hearing loss is associated with ongoing viral replication in the inner ear up to years after birth.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Allergy and Immunology</subject><subject>Biological and medical sciences</subject><subject>Birth</subject><subject>Blood - virology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cochlear implant</subject><subject>Cochlear Implants</subject><subject>Congenital cytomegalovirus</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - classification</subject><subject>Cytomegalovirus - genetics</subject><subject>Cytomegalovirus - isolation &amp; purification</subject><subject>Cytomegalovirus Infections - congenital</subject><subject>Cytomegalovirus Infections - virology</subject><subject>Deafness - etiology</subject><subject>Deafness - virology</subject><subject>Desiccation</subject><subject>DNA, Viral - genetics</subject><subject>DNA, Viral - isolation &amp; purification</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genotype</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infectious Disease</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Perilymph - virology</subject><subject>Specimen Handling - methods</subject><subject>Viral diseases</subject><subject>Virology</subject><subject>Young Adult</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks2KFDEQgBtR3HX1AbxILoKXHvPTnaQRhGX8hUUP6jmkk_ROxnSnTdIj8yi-rdXMqOBBPCWpfFUV6ktVPSZ4QzDhz_ebvTlsKCYUzhuM5Z3qkkjB6rbj4i7smeQ1bxm9qB7kvMeYtKwR96sLykhDOoYvqx_bY4mju9UhHnxaMnr14RpZV5wpPk7IT8gm7yzqQ4wW5TmWjPRk0eySD8dx3uniDRrC4m1GQ4oj3FivS4Loymm7hIJMNLvgdEJ-nIOeCkrO-Nm7Cap992WH5uSCn24XHaC5HiaX88Pq3qBDdo_O61X15c3rz9t39c3Ht--31ze1aQQpNeOOm87hltOeYdaxRktjeisklkNHTYMp69uOWKENH1pMRW-Mpo3FljawY1fVs1PdOcVvi8tFjT4bF-CdLi5ZESpYi7kg5H9QgBspKaDkhJoUc05uUHPyo05HRbBa5am9AnlqlbeGQB7kPDmXX_rR2d8Zv2wB8PQM6Gx0GJKejM9_OC4ZllwA9-LEOZjbwbuksoFhGzADgy_KRv_PZ7z8K9uAGw8Nv7qjy_u4pAmEKKIyVVh9Wn_Z-skIxZjJTrCfet_O6Q</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>de Vries, Jutte J.C</creator><creator>Vesseur, Annemarie</creator><creator>Rotteveel, Liselotte J.C</creator><creator>Korver, Anna M.H</creator><creator>Rusman, Lisette G</creator><creator>Wessels, Els</creator><creator>Kroes, Aloys C.M</creator><creator>Mylanus, Emmanuel A</creator><creator>Oudesluys-Murphy, Anne M</creator><creator>Frijns, Johan H.M</creator><creator>Vossen, Ann C.T.M</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20130201</creationdate><title>Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness</title><author>de Vries, Jutte J.C ; Vesseur, Annemarie ; Rotteveel, Liselotte J.C ; Korver, Anna M.H ; Rusman, Lisette G ; Wessels, Els ; Kroes, Aloys C.M ; Mylanus, Emmanuel A ; Oudesluys-Murphy, Anne M ; Frijns, Johan H.M ; Vossen, Ann C.T.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-36e6c9e0562b303934a8ccbd7808f92c4023b591d7ac6f5027bcca24d0d24cca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Allergy and Immunology</topic><topic>Biological and medical sciences</topic><topic>Birth</topic><topic>Blood - virology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cochlear implant</topic><topic>Cochlear Implants</topic><topic>Congenital cytomegalovirus</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus - classification</topic><topic>Cytomegalovirus - genetics</topic><topic>Cytomegalovirus - isolation &amp; purification</topic><topic>Cytomegalovirus Infections - congenital</topic><topic>Cytomegalovirus Infections - virology</topic><topic>Deafness - etiology</topic><topic>Deafness - virology</topic><topic>Desiccation</topic><topic>DNA, Viral - genetics</topic><topic>DNA, Viral - isolation &amp; purification</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genotype</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Perilymph - virology</topic><topic>Specimen Handling - methods</topic><topic>Viral diseases</topic><topic>Virology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Vries, Jutte J.C</creatorcontrib><creatorcontrib>Vesseur, Annemarie</creatorcontrib><creatorcontrib>Rotteveel, Liselotte J.C</creatorcontrib><creatorcontrib>Korver, Anna M.H</creatorcontrib><creatorcontrib>Rusman, Lisette G</creatorcontrib><creatorcontrib>Wessels, Els</creatorcontrib><creatorcontrib>Kroes, Aloys C.M</creatorcontrib><creatorcontrib>Mylanus, Emmanuel A</creatorcontrib><creatorcontrib>Oudesluys-Murphy, Anne M</creatorcontrib><creatorcontrib>Frijns, Johan H.M</creatorcontrib><creatorcontrib>Vossen, Ann C.T.M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Vries, Jutte J.C</au><au>Vesseur, Annemarie</au><au>Rotteveel, Liselotte J.C</au><au>Korver, Anna M.H</au><au>Rusman, Lisette G</au><au>Wessels, Els</au><au>Kroes, Aloys C.M</au><au>Mylanus, Emmanuel A</au><au>Oudesluys-Murphy, Anne M</au><au>Frijns, Johan H.M</au><au>Vossen, Ann C.T.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>56</volume><issue>2</issue><spage>113</spage><epage>117</epage><pages>113-117</pages><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>Abstract Background Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic congenital hearing loss. The contribution of congenital CMV to prelingual deafness and the pathophysiology is largely unknown. Objective (1) To analyze the prevalence of congenital CMV among cochlear implant (CI) recipients with prelingual deafness. (2) To genotype CMV present in dried blood spots (DBS) and in the inner ear years after birth. Study design Children and adults with prelingual deafness who received a CI in 2010–2011 were included prospectively. Perilymphatic fluids were collected during CI surgery and, in the pediatric cases, DBS were retrieved for CMV DNA detection. Furthermore, a cohort of children with prelingual deafness who received a CI between 2003 and 2008 were included retrospectively. CMV detection in DBS and perilymph was followed by gB and gH genotyping. Results Seventysix pediatric CI recipients were included. Seventy DBS were tested for CMV DNA, resulting in a prevalence of congenital CMV of 14% (10/70). Perilymphatic fluid was available from 29 pediatric CI recipients. One perilymph fluid, of a 21-month old girl with congenital CMV, asymptomatic at birth, was CMV DNA positive. The CMV strain in the perilymph was genotypically identical to the strain present in her DBS (gB1/gH2). Perilymph samples from 21 adult CI recipients were CMV DNA negative. Conclusions Our study stresses the important contribution of congenital CMV among pediatric CI recipients. Furthermore, our genotyping data support the hypothesis that CMV-related hearing loss is associated with ongoing viral replication in the inner ear up to years after birth.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23141930</pmid><doi>10.1016/j.jcv.2012.10.008</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1386-6532
ispartof Journal of clinical virology, 2013-02, Vol.56 (2), p.113-117
issn 1386-6532
1873-5967
language eng
recordid cdi_proquest_miscellaneous_1273506711
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adolescent
Adult
Allergy and Immunology
Biological and medical sciences
Birth
Blood - virology
Child
Child, Preschool
Cochlear implant
Cochlear Implants
Congenital cytomegalovirus
Cytomegalovirus
Cytomegalovirus - classification
Cytomegalovirus - genetics
Cytomegalovirus - isolation & purification
Cytomegalovirus Infections - congenital
Cytomegalovirus Infections - virology
Deafness - etiology
Deafness - virology
Desiccation
DNA, Viral - genetics
DNA, Viral - isolation & purification
Female
Fundamental and applied biological sciences. Psychology
Genotype
Human viral diseases
Humans
Infant
Infant, Newborn
Infectious Disease
Infectious diseases
Male
Medical sciences
Microbiology
Middle Aged
Miscellaneous
Perilymph - virology
Specimen Handling - methods
Viral diseases
Virology
Young Adult
title Cytomegalovirus DNA detection in dried blood spots and perilymphatic fluids from pediatric and adult cochlear implant recipients with prelingual deafness
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T17%3A27%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cytomegalovirus%20DNA%20detection%20in%20dried%20blood%20spots%20and%20perilymphatic%20fluids%20from%20pediatric%20and%20adult%20cochlear%20implant%20recipients%20with%20prelingual%20deafness&rft.jtitle=Journal%20of%20clinical%20virology&rft.au=de%20Vries,%20Jutte%20J.C&rft.date=2013-02-01&rft.volume=56&rft.issue=2&rft.spage=113&rft.epage=117&rft.pages=113-117&rft.issn=1386-6532&rft.eissn=1873-5967&rft_id=info:doi/10.1016/j.jcv.2012.10.008&rft_dat=%3Cproquest_cross%3E1273506711%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1272734882&rft_id=info:pmid/23141930&rft_els_id=S1386653212003897&rfr_iscdi=true