Please use this identifier to cite or link to this item: https://doi.org/10.1586/ern.11.114
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dc.titleAntiganglioside antibodies in Guillain-Barré syndrome and its related conditions
dc.contributor.authorShahrizaila, N.
dc.contributor.authorYuki, N.
dc.date.accessioned2016-09-06T08:19:35Z
dc.date.available2016-09-06T08:19:35Z
dc.date.issued2011-09
dc.identifier.citationShahrizaila, N., Yuki, N. (2011-09). Antiganglioside antibodies in Guillain-Barré syndrome and its related conditions. Expert Review of Neurotherapeutics 11 (9) : 1305-1313. ScholarBank@NUS Repository. https://doi.org/10.1586/ern.11.114
dc.identifier.issn14737175
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/126767
dc.description.abstractGuillain-Barré syndrome (GBS) is typically classified into two major subtypes: acute inflammatory demyelinating neuropathy and acute motor axonal neuropathy. Its most recognizable variant is Fisher syndrome. The last two decades have seen considerable advances in our understanding of GBS. Of note, various autoantibodies against ganglioside antigens have been identified and found to have significant associations with the axonal forms of GBS and Fisher syndrome. In this article, we discuss the different clinical presentations in GBS and the role of antiganglioside antibodies in their underlying pathogenesis. We also discuss the impact that antiganglioside antibodies have had in the development of experimental models and treatment modalities in GBS. © 2011 Expert Reviews Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1586/ern.11.114
dc.sourceScopus
dc.subjectantiganglioside antibodies
dc.subjectFisher syndrome
dc.subjectGuillain-Barré syndrome
dc.typeReview
dc.contributor.departmentMICROBIOLOGY
dc.description.doi10.1586/ern.11.114
dc.description.sourcetitleExpert Review of Neurotherapeutics
dc.description.volume11
dc.description.issue9
dc.description.page1305-1313
dc.description.codenERNXA
dc.identifier.isiut000295216900015
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