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dc.contributor.authorKiyat-Atamer, A.
dc.contributor.authorTuzun, Erdem
dc.contributor.authorDeymeer, F.
dc.contributor.authorOflazer, P.
dc.contributor.authorShugaiv, E.
dc.contributor.authorAkman-Demir, G.
dc.contributor.authorParman, Y.
dc.date.accessioned2021-03-05T13:45:34Z
dc.date.available2021-03-05T13:45:34Z
dc.date.issued2013
dc.identifier.citationShugaiv E., Kiyat-Atamer A., Tuzun E., Deymeer F., Oflazer P., Parman Y., Akman-Demir G., "Coexistence of Guillain-Barre syndrome and Behcet's disease", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.31, 2013
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_b3bcc76f-2ca8-4425-82a1-ff1db5c88d30
dc.identifier.urihttp://hdl.handle.net/20.500.12627/119706
dc.description.abstractBehcet's disease (BD) is a multisystemic, recurrent and inflammatory disorder. Neurological involvement is rare and affects mainly the central nervous system (CNS) in the form of brainstem meningoencephalitis or dural sinus thrombosis. Peripheral neuropathy is usually not observed during the course of BD but some reports have shown electrophysiologic evidence of subclinical neuropathy, mononeuritis multiplex and cranial neuropathy in BD patients. The co-occurrence of Guillain-Barre syndrome (GBS), an acute inflammatory demyelinating neuropathy, with other autoimmune or systemic diseases is rare. We present a case of BD with clinical and electrophysiological diagnosis of GBS. The findings of the patient were discussed with reference to literature.
dc.language.isoeng
dc.subjectROMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.titleCoexistence of Guillain-Barre syndrome and Behcet's disease
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.departmentİstanbul Bilim Üniversitesi , ,
dc.identifier.volume31
dc.identifier.issue3
dc.contributor.firstauthorID2163


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