Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies
The classic cardiac manifestation of neonatal lupus is congenitalheart block, attributed to antibodymediated inflammation and subsequent fibrosis of the atrioventricular(AV) node. In consideringthe pathologic process of injury it may be that tissue damage results in a range of conduction abnormaliti...
Gespeichert in:
Veröffentlicht in: | Lupus 2002-01, Vol.11 (3), p.145-151 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 151 |
---|---|
container_issue | 3 |
container_start_page | 145 |
container_title | Lupus |
container_volume | 11 |
creator | Askanase, A D Friedman, D M Copel, J Dische, M R Dubin, A Starc, T J Katholi, M C Buyon, J P |
description | The classic cardiac manifestation of neonatal lupus is congenitalheart block, attributed to antibodymediated inflammation and subsequent fibrosis of the atrioventricular(AV) node. In consideringthe pathologic process of injury it may be that tissue damage results in a range of conduction abnormalities. Identification of less-advanced degrees of block or of fibrosis around the AV node without any conduction abnormality on EKG would support this pathologic model, and serve as a potential marker for treatment if the conduction defect could be shown to progress. To ascertain the spectrum of arrhythmias associated with maternal anti-SSA/Ro-SSB/La antibodies, records of all children enrolled in the Research Registry for Neonatal Lupus were reviewed. Of 187 children with congenital heart block whose mothers have anti-SSA/Ro-SSB/La antibodies, nine had a prolonged PR interval on EKG at birth, four of whom progressed to more advanced AV block. A child whose younger sibling had third degree block was diagnosed with first degree block at age 10 years at the time of surgery for a broken wrist. Two children diagnosed in utero with second degree block were treated with dexamethasone and reverted to normal sinus rhythm by birth, but ultimately progressed to third degree block. Four children had second degree block at birth: of these, two progressed to third degree block. Sinus bradycardia (< 100 bpm) was present in three (3.8%) of 78 fetuses for whom atrial rates were recorded by echocardiogram. Of 40 neonates for whom EKGs were available, the mean atrial rate was 137± 20 bpm (range 75–200). These data have important research and clinical implications. In contrast to the AV node, permanent sinoatrial nodal involvement is not clinically apparent. Perhaps many fetuses sustain mild inflammation, but resolution is variable, as suggested by the presence of incomplete AV block. Since subsequent progression of less-advanced degrees of block can occur, an EKG should be performed on all infants born to mothers with anti-SSA/Ro-SSB/La antibodies. |
doi_str_mv | 10.1191/0961203302lu173oa |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71671430</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1191_0961203302lu173oa</sage_id><sourcerecordid>71671430</sourcerecordid><originalsourceid>FETCH-LOGICAL-c394t-300e0b7768f7caee38bc04e24d9836181aebcaa38c1deb661bd9ca94fcfb4b113</originalsourceid><addsrcrecordid>eNqFkV9L5DAUxYO46PjnA_giwYd9q5PbdJrmUQdXhYGFnfW5JOmtVtpkTFLEb2_qDAjKsnDhcnN_54TLIeQM2CWAhDmTJeSMc5b3Iwju1B6ZQSFElhb5PplN-2wCDslRCM-MMQ6yPCCHSS1lJeSM-PUGTfTjQJVt6Ma7R48hdM5S11LjbDOaOE1KW-cH1Xexw0A7m6pVNgaqnbc0Ojq4-IQ-0NcuPiWv2GXr9dX8j0vter5SH0_aNUl9Qn60qg94uuvH5OHXzd_lXbb6fXu_vFplhssiZpwxZFqIsmqFUYi80oYVmBeNrHgJFSjURileGWhQlyXoRholi9a0utAA_Jj83Pqmq15GDLEeumCw75VFN4ZaQCmg4Oy_IFRcLqp8kcCLL-CzG71NR9R5npd8IeTkBlvIeBeCx7be-G5Q_q0GVk-x1d9iS5rznfGoB2w-FbucEnC5BYJ6xM9f_-34DkrMovw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222635790</pqid></control><display><type>article</type><title>Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies</title><source>SAGE Complete A-Z List</source><source>MEDLINE</source><creator>Askanase, A D ; Friedman, D M ; Copel, J ; Dische, M R ; Dubin, A ; Starc, T J ; Katholi, M C ; Buyon, J P</creator><creatorcontrib>Askanase, A D ; Friedman, D M ; Copel, J ; Dische, M R ; Dubin, A ; Starc, T J ; Katholi, M C ; Buyon, J P</creatorcontrib><description>The classic cardiac manifestation of neonatal lupus is congenitalheart block, attributed to antibodymediated inflammation and subsequent fibrosis of the atrioventricular(AV) node. In consideringthe pathologic process of injury it may be that tissue damage results in a range of conduction abnormalities. Identification of less-advanced degrees of block or of fibrosis around the AV node without any conduction abnormality on EKG would support this pathologic model, and serve as a potential marker for treatment if the conduction defect could be shown to progress. To ascertain the spectrum of arrhythmias associated with maternal anti-SSA/Ro-SSB/La antibodies, records of all children enrolled in the Research Registry for Neonatal Lupus were reviewed. Of 187 children with congenital heart block whose mothers have anti-SSA/Ro-SSB/La antibodies, nine had a prolonged PR interval on EKG at birth, four of whom progressed to more advanced AV block. A child whose younger sibling had third degree block was diagnosed with first degree block at age 10 years at the time of surgery for a broken wrist. Two children diagnosed in utero with second degree block were treated with dexamethasone and reverted to normal sinus rhythm by birth, but ultimately progressed to third degree block. Four children had second degree block at birth: of these, two progressed to third degree block. Sinus bradycardia (< 100 bpm) was present in three (3.8%) of 78 fetuses for whom atrial rates were recorded by echocardiogram. Of 40 neonates for whom EKGs were available, the mean atrial rate was 137± 20 bpm (range 75–200). These data have important research and clinical implications. In contrast to the AV node, permanent sinoatrial nodal involvement is not clinically apparent. Perhaps many fetuses sustain mild inflammation, but resolution is variable, as suggested by the presence of incomplete AV block. Since subsequent progression of less-advanced degrees of block can occur, an EKG should be performed on all infants born to mothers with anti-SSA/Ro-SSB/La antibodies.</description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1191/0961203302lu173oa</identifier><identifier>PMID: 11999879</identifier><language>eng</language><publisher>Thousand Oaks, CA: SAGE Publications</publisher><subject>Antibodies ; Antibodies, Antinuclear - immunology ; Antigens ; Autoantigens ; Autoimmune Diseases - immunology ; Autoimmune Diseases - pathology ; Autoimmune Diseases - physiopathology ; Cardiac arrhythmia ; Cardiology ; Child, Preschool ; Children & youth ; Congenital diseases ; Electrocardiography ; Female ; Fetuses ; Fibrosis - pathology ; Heart ; Heart Block - immunology ; Heart Block - pathology ; Heart Block - physiopathology ; Heart Defects, Congenital - immunology ; Heart Defects, Congenital - pathology ; Heart Defects, Congenital - physiopathology ; Hospitals ; Humans ; Hypotheses ; Infant ; Infant, Newborn ; Lupus ; Male ; Medicine ; Mothers ; Myocardium - pathology ; Pediatrics ; Pregnancy ; Rheumatology ; Ribonucleoproteins - immunology ; RNA, Small Cytoplasmic ; Sinuses ; SS-B Antigen ; Ultrasonic imaging</subject><ispartof>Lupus, 2002-01, Vol.11 (3), p.145-151</ispartof><rights>2002 Arnold</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-300e0b7768f7caee38bc04e24d9836181aebcaa38c1deb661bd9ca94fcfb4b113</citedby><cites>FETCH-LOGICAL-c394t-300e0b7768f7caee38bc04e24d9836181aebcaa38c1deb661bd9ca94fcfb4b113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1191/0961203302lu173oa$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1191/0961203302lu173oa$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11999879$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Askanase, A D</creatorcontrib><creatorcontrib>Friedman, D M</creatorcontrib><creatorcontrib>Copel, J</creatorcontrib><creatorcontrib>Dische, M R</creatorcontrib><creatorcontrib>Dubin, A</creatorcontrib><creatorcontrib>Starc, T J</creatorcontrib><creatorcontrib>Katholi, M C</creatorcontrib><creatorcontrib>Buyon, J P</creatorcontrib><title>Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies</title><title>Lupus</title><addtitle>Lupus</addtitle><description>The classic cardiac manifestation of neonatal lupus is congenitalheart block, attributed to antibodymediated inflammation and subsequent fibrosis of the atrioventricular(AV) node. In consideringthe pathologic process of injury it may be that tissue damage results in a range of conduction abnormalities. Identification of less-advanced degrees of block or of fibrosis around the AV node without any conduction abnormality on EKG would support this pathologic model, and serve as a potential marker for treatment if the conduction defect could be shown to progress. To ascertain the spectrum of arrhythmias associated with maternal anti-SSA/Ro-SSB/La antibodies, records of all children enrolled in the Research Registry for Neonatal Lupus were reviewed. Of 187 children with congenital heart block whose mothers have anti-SSA/Ro-SSB/La antibodies, nine had a prolonged PR interval on EKG at birth, four of whom progressed to more advanced AV block. A child whose younger sibling had third degree block was diagnosed with first degree block at age 10 years at the time of surgery for a broken wrist. Two children diagnosed in utero with second degree block were treated with dexamethasone and reverted to normal sinus rhythm by birth, but ultimately progressed to third degree block. Four children had second degree block at birth: of these, two progressed to third degree block. Sinus bradycardia (< 100 bpm) was present in three (3.8%) of 78 fetuses for whom atrial rates were recorded by echocardiogram. Of 40 neonates for whom EKGs were available, the mean atrial rate was 137± 20 bpm (range 75–200). These data have important research and clinical implications. In contrast to the AV node, permanent sinoatrial nodal involvement is not clinically apparent. Perhaps many fetuses sustain mild inflammation, but resolution is variable, as suggested by the presence of incomplete AV block. Since subsequent progression of less-advanced degrees of block can occur, an EKG should be performed on all infants born to mothers with anti-SSA/Ro-SSB/La antibodies.</description><subject>Antibodies</subject><subject>Antibodies, Antinuclear - immunology</subject><subject>Antigens</subject><subject>Autoantigens</subject><subject>Autoimmune Diseases - immunology</subject><subject>Autoimmune Diseases - pathology</subject><subject>Autoimmune Diseases - physiopathology</subject><subject>Cardiac arrhythmia</subject><subject>Cardiology</subject><subject>Child, Preschool</subject><subject>Children & youth</subject><subject>Congenital diseases</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Fetuses</subject><subject>Fibrosis - pathology</subject><subject>Heart</subject><subject>Heart Block - immunology</subject><subject>Heart Block - pathology</subject><subject>Heart Block - physiopathology</subject><subject>Heart Defects, Congenital - immunology</subject><subject>Heart Defects, Congenital - pathology</subject><subject>Heart Defects, Congenital - physiopathology</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lupus</subject><subject>Male</subject><subject>Medicine</subject><subject>Mothers</subject><subject>Myocardium - pathology</subject><subject>Pediatrics</subject><subject>Pregnancy</subject><subject>Rheumatology</subject><subject>Ribonucleoproteins - immunology</subject><subject>RNA, Small Cytoplasmic</subject><subject>Sinuses</subject><subject>SS-B Antigen</subject><subject>Ultrasonic imaging</subject><issn>0961-2033</issn><issn>1477-0962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkV9L5DAUxYO46PjnA_giwYd9q5PbdJrmUQdXhYGFnfW5JOmtVtpkTFLEb2_qDAjKsnDhcnN_54TLIeQM2CWAhDmTJeSMc5b3Iwju1B6ZQSFElhb5PplN-2wCDslRCM-MMQ6yPCCHSS1lJeSM-PUGTfTjQJVt6Ma7R48hdM5S11LjbDOaOE1KW-cH1Xexw0A7m6pVNgaqnbc0Ojq4-IQ-0NcuPiWv2GXr9dX8j0vter5SH0_aNUl9Qn60qg94uuvH5OHXzd_lXbb6fXu_vFplhssiZpwxZFqIsmqFUYi80oYVmBeNrHgJFSjURileGWhQlyXoRholi9a0utAA_Jj83Pqmq15GDLEeumCw75VFN4ZaQCmg4Oy_IFRcLqp8kcCLL-CzG71NR9R5npd8IeTkBlvIeBeCx7be-G5Q_q0GVk-x1d9iS5rznfGoB2w-FbucEnC5BYJ6xM9f_-34DkrMovw</recordid><startdate>20020101</startdate><enddate>20020101</enddate><creator>Askanase, A D</creator><creator>Friedman, D M</creator><creator>Copel, J</creator><creator>Dische, M R</creator><creator>Dubin, A</creator><creator>Starc, T J</creator><creator>Katholi, M C</creator><creator>Buyon, J P</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20020101</creationdate><title>Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies</title><author>Askanase, A D ; Friedman, D M ; Copel, J ; Dische, M R ; Dubin, A ; Starc, T J ; Katholi, M C ; Buyon, J P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-300e0b7768f7caee38bc04e24d9836181aebcaa38c1deb661bd9ca94fcfb4b113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Antibodies</topic><topic>Antibodies, Antinuclear - immunology</topic><topic>Antigens</topic><topic>Autoantigens</topic><topic>Autoimmune Diseases - immunology</topic><topic>Autoimmune Diseases - pathology</topic><topic>Autoimmune Diseases - physiopathology</topic><topic>Cardiac arrhythmia</topic><topic>Cardiology</topic><topic>Child, Preschool</topic><topic>Children & youth</topic><topic>Congenital diseases</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Fetuses</topic><topic>Fibrosis - pathology</topic><topic>Heart</topic><topic>Heart Block - immunology</topic><topic>Heart Block - pathology</topic><topic>Heart Block - physiopathology</topic><topic>Heart Defects, Congenital - immunology</topic><topic>Heart Defects, Congenital - pathology</topic><topic>Heart Defects, Congenital - physiopathology</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Lupus</topic><topic>Male</topic><topic>Medicine</topic><topic>Mothers</topic><topic>Myocardium - pathology</topic><topic>Pediatrics</topic><topic>Pregnancy</topic><topic>Rheumatology</topic><topic>Ribonucleoproteins - immunology</topic><topic>RNA, Small Cytoplasmic</topic><topic>Sinuses</topic><topic>SS-B Antigen</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Askanase, A D</creatorcontrib><creatorcontrib>Friedman, D M</creatorcontrib><creatorcontrib>Copel, J</creatorcontrib><creatorcontrib>Dische, M R</creatorcontrib><creatorcontrib>Dubin, A</creatorcontrib><creatorcontrib>Starc, T J</creatorcontrib><creatorcontrib>Katholi, M C</creatorcontrib><creatorcontrib>Buyon, J P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Askanase, A D</au><au>Friedman, D M</au><au>Copel, J</au><au>Dische, M R</au><au>Dubin, A</au><au>Starc, T J</au><au>Katholi, M C</au><au>Buyon, J P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2002-01-01</date><risdate>2002</risdate><volume>11</volume><issue>3</issue><spage>145</spage><epage>151</epage><pages>145-151</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract>The classic cardiac manifestation of neonatal lupus is congenitalheart block, attributed to antibodymediated inflammation and subsequent fibrosis of the atrioventricular(AV) node. In consideringthe pathologic process of injury it may be that tissue damage results in a range of conduction abnormalities. Identification of less-advanced degrees of block or of fibrosis around the AV node without any conduction abnormality on EKG would support this pathologic model, and serve as a potential marker for treatment if the conduction defect could be shown to progress. To ascertain the spectrum of arrhythmias associated with maternal anti-SSA/Ro-SSB/La antibodies, records of all children enrolled in the Research Registry for Neonatal Lupus were reviewed. Of 187 children with congenital heart block whose mothers have anti-SSA/Ro-SSB/La antibodies, nine had a prolonged PR interval on EKG at birth, four of whom progressed to more advanced AV block. A child whose younger sibling had third degree block was diagnosed with first degree block at age 10 years at the time of surgery for a broken wrist. Two children diagnosed in utero with second degree block were treated with dexamethasone and reverted to normal sinus rhythm by birth, but ultimately progressed to third degree block. Four children had second degree block at birth: of these, two progressed to third degree block. Sinus bradycardia (< 100 bpm) was present in three (3.8%) of 78 fetuses for whom atrial rates were recorded by echocardiogram. Of 40 neonates for whom EKGs were available, the mean atrial rate was 137± 20 bpm (range 75–200). These data have important research and clinical implications. In contrast to the AV node, permanent sinoatrial nodal involvement is not clinically apparent. Perhaps many fetuses sustain mild inflammation, but resolution is variable, as suggested by the presence of incomplete AV block. Since subsequent progression of less-advanced degrees of block can occur, an EKG should be performed on all infants born to mothers with anti-SSA/Ro-SSB/La antibodies.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>11999879</pmid><doi>10.1191/0961203302lu173oa</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0961-2033 |
ispartof | Lupus, 2002-01, Vol.11 (3), p.145-151 |
issn | 0961-2033 1477-0962 |
language | eng |
recordid | cdi_proquest_miscellaneous_71671430 |
source | SAGE Complete A-Z List; MEDLINE |
subjects | Antibodies Antibodies, Antinuclear - immunology Antigens Autoantigens Autoimmune Diseases - immunology Autoimmune Diseases - pathology Autoimmune Diseases - physiopathology Cardiac arrhythmia Cardiology Child, Preschool Children & youth Congenital diseases Electrocardiography Female Fetuses Fibrosis - pathology Heart Heart Block - immunology Heart Block - pathology Heart Block - physiopathology Heart Defects, Congenital - immunology Heart Defects, Congenital - pathology Heart Defects, Congenital - physiopathology Hospitals Humans Hypotheses Infant Infant, Newborn Lupus Male Medicine Mothers Myocardium - pathology Pediatrics Pregnancy Rheumatology Ribonucleoproteins - immunology RNA, Small Cytoplasmic Sinuses SS-B Antigen Ultrasonic imaging |
title | Spectrum and progression of conduction abnormalities in infants born to mothers with anti-SSA/Ro-SSB/La antibodies |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T13%3A44%3A50IST&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=Spectrum%20and%20progression%20of%20conduction%20abnormalities%20in%20infants%20born%20to%20mothers%20with%20anti-SSA/Ro-SSB/La%20antibodies&rft.jtitle=Lupus&rft.au=Askanase,%20A%20D&rft.date=2002-01-01&rft.volume=11&rft.issue=3&rft.spage=145&rft.epage=151&rft.pages=145-151&rft.issn=0961-2033&rft.eissn=1477-0962&rft_id=info:doi/10.1191/0961203302lu173oa&rft_dat=%3Cproquest_cross%3E71671430%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=222635790&rft_id=info:pmid/11999879&rft_sage_id=10.1191_0961203302lu173oa&rfr_iscdi=true |