A case of autoimmune limbic encephalitis in a patient with Behcet’s disease
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Behcet’s disease is well known to have neurological manifestations, most usually as a consequence of focal parenchymal lesions or vascular thrombosis. We report a case of autoimmune limbic encephalitis in a patient with Behcet’s disease, that was highly responsive to immunoglobulins and steroid, which ultimately prevented mortality, and reduced comorbidity. We also review the investigation and management of non-paraneoplastic, or autoimmune limbic encephalitis.
2013 ◽
Vol 115
(10)
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pp. 2015-2018
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2020 ◽
Vol 154
(12)
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pp. 488-492
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2006 ◽
Vol 116
(3)
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pp. 281-287
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2005 ◽
Vol 206
(1)
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pp. 15-22
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2005 ◽
Vol 207
(1)
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pp. 1-2
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2019 ◽
Vol 15
(5)
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pp. e36-e38
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2010 ◽
Vol 257
(6)
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pp. 1012-1020
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