{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:36:01Z","timestamp":1787841361038,"version":"build-2784847793"},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2021,1]]},"abstract":"<jats:sec>\n                    <jats:title>Background:<\/jats:title>\n                    <jats:p>Anti \u03b1-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) encephalitis is a rare autoimmune encephalitis. They present with memory, confusion or behavioral changes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>The aim of this study was to describe unusual clinical features in a patient with AMPAR-associated encephalitis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case:<\/jats:title>\n                    <jats:p>A 42-year-old female presented to us with bulbar and gait disturbances of three weeks duration and behavioral changes for ten days. She was found to have memory impairment along with psychosis. She had left eye ptosis, restricted eye movements, sluggish deep tendon reflexes, and bilateral cerebellar signs. Her serum and CSF (cerebrospinal fluid) AMPAR2 antibodies were strongly positive; CT (computed tomography) chest showed evidence of Thymoma. She was treated with steroids with significant improvement initially but expired within 3 months of diagnosis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>This is the first report of AMPAR associated encephalitis from India presenting with unique clinical features affecting both the CNS (central nervous system)\u2013\u2013(psychosis, ataxia, cognition) and PNS\u2013\u2013peripheral nervous system involvement (ptosis, restricted eye movements, bulbar disturbances).<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/0028-3886.310087","type":"journal-article","created":{"date-parts":[[2021,4,26]],"date-time":"2021-04-26T01:22:00Z","timestamp":1619400120000},"page":"149-152","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":6,"title":["A Rare Case of Wobbly, Psychotic Patient with Frozen Eyes - Anti-AMPA Receptor Encephalitis"],"prefix":"10.4103","volume":"69","author":[{"given":"V R","family":"Ashok","sequence":"first","affiliation":[{"name":"Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Nagabushana","sequence":"additional","affiliation":[{"name":"Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G","family":"Yashwanth","sequence":"additional","affiliation":[{"name":"Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A","family":"Mahadevan","sequence":"additional","affiliation":[{"name":"Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Netravathi","sequence":"additional","affiliation":[{"name":"Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2021,2,24]]},"reference":[{"key":"R1-20250925","doi-asserted-by":"crossref","first-page":"687","DOI":"10.4103\/0028-3886.166532","article-title":"Clinical and imaging characteristics of 16 patients with autoimmune neuronal synaptic encephalitis","volume":"63","author":"Kamble","year":"2015","journal-title":"Neurol India"},{"key":"R2-20250925","doi-asserted-by":"crossref","first-page":"424","DOI":"10.1002\/ana.21589","article-title":"AMPA receptor antibodies in limbic encephalitis alter synaptic receptor location","volume":"65","author":"Lai","year":"2009","journal-title":"Ann 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Neurol"},{"key":"R6-20250925","doi-asserted-by":"crossref","first-page":"e01528","DOI":"10.1002\/brb3.1528","article-title":"LE associated with AMPA receptor and CRMP5 antibodies: A case report and literature review","volume":"00","author":"Jia","year":"2020","journal-title":"Brain Behav"},{"key":"R7-20250925","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1016\/j.jneuroim.2015.02.011","article-title":"Anti-AMPA receptor encephalitis associated with thymomatous MG","volume":"281","author":"Li","journal-title":"J Neuroimmunol"}],"container-title":["Neurology 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