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dc.contributor.authorROSSI, Jeffrey E.
dc.contributor.authorTuzun, Erdem
dc.contributor.authorDALMAU, Josep
dc.contributor.authorCENTURION, Alejandro F.
dc.contributor.authorKARNER, Steve F.
dc.date.accessioned2021-03-05T14:08:52Z
dc.date.available2021-03-05T14:08:52Z
dc.identifier.citationTuzun E., ROSSI J. E. , KARNER S. F. , CENTURION A. F. , DALMAU J., "Adenylate kinase 5 autoimmunity in treatment refractory limbic encephalitis", JOURNAL OF NEUROIMMUNOLOGY, cilt.186, ss.177-180, 2007
dc.identifier.issn0165-5728
dc.identifier.othervv_1032021
dc.identifier.otherav_b5b66ef2-b80a-4ee1-aeb1-1b5926453690
dc.identifier.urihttp://hdl.handle.net/20.500.12627/120950
dc.identifier.urihttps://doi.org/10.1016/j.jneuroim.2007.03.015
dc.description.abstractWe report two men with limbic encephalitis (LE) refractory to corticosteroids, Wig and plasma exchange. Both patients had serum/CSF antibodies that reacted with the cytoplasm of neurons. Probing of a hippocampal cDNA library resulted in the isolation of adenylate kinase 5 (AK5). Patients' antibodies, but not those of 111 controls, recognized AK5-expressing phage plaques. Human AK5-affinity purified antibodies reproduced the neuronal immunolabeling of patients' antibodies, and co-localized with a rabbit AK5 antibody, confirming that the brain autoantigen was AK5. Detection of antibodies to AK5 in LE patients carries a poor prognosis, and suggests the prompt use of aggressive immunosuppression. (c) 2007 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectTemel Bilimler
dc.subjectİmmünoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.titleAdenylate kinase 5 autoimmunity in treatment refractory limbic encephalitis
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROIMMUNOLOGY
dc.contributor.department, ,
dc.identifier.volume186
dc.identifier.startpage177
dc.identifier.endpage180
dc.contributor.firstauthorID1830


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