{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T14:31:43Z","timestamp":1790260303898,"version":"4.1.0"},"reference-count":35,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2014,3,6]],"date-time":"2014-03-06T00:00:00Z","timestamp":1394064000000},"content-version":"vor","delay-in-days":5,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Peripheral Nervous Sys"],"published-print":{"date-parts":[[2014,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>There is a paucity of large studies evaluating the subtypes of Guillain\u2010Barr\u00e9 syndrome (<jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content>) and their outcome from Southeast Asia. We report cliniconeurophysiological subtypes of <jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content> and their correlation with triggering events and 3\u2010month outcome from northern India. Three hundred and twenty eight consecutive patients with <jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content> were clinically evaluated, including their triggers, severity, autonomic involvement, cranial nerve palsy, and respiratory paralysis. Nerve conduction study (<jats:styled-content style=\"fixed-case\">NCS<\/jats:styled-content>) was repeated at 3\u2009weeks if the initial study was normal. They were categorized into acute inflammatory demyelinating polyradiculoneuropathy (<jats:styled-content style=\"fixed-case\">AIDP<\/jats:styled-content>), acute motor axonal neuropathy (<jats:styled-content style=\"fixed-case\">AMAN<\/jats:styled-content>), acute motor sensory axonal neuropathy (<jats:styled-content style=\"fixed-case\">AMSAN<\/jats:styled-content>), inexcitable motor nerve, and equivocal. Clinically, 204 (62.2%) patients had pure motor, 106 (32.3%) motor sensory, 16 (4.9%) Miller Fisher syndrome, and 2 (0.6%) pure sensory <jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content>. Based on <jats:styled-content style=\"fixed-case\">NCS<\/jats:styled-content>, 242 (73.8%) had <jats:styled-content style=\"fixed-case\">AIDP<\/jats:styled-content>, 44 (13.4%) <jats:styled-content style=\"fixed-case\">AMAN<\/jats:styled-content>, 15 (4.6%) <jats:styled-content style=\"fixed-case\">AMSAN<\/jats:styled-content>, 8 (2.4%) inexcitable motor nerves, and 27 (8.2%) equivocal <jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">AIDP<\/jats:styled-content> patients were older, more common in summer, had lesser peak disability, and better outcome compared to those with <jats:styled-content style=\"fixed-case\">AMAN<\/jats:styled-content>. Eleven (3.4%) patients died and 48 (14.6%) had poor outcome at 3\u2009months. The poor outcome was related to severity, dysautonomia, and inexcitable motor nerves. <jats:styled-content style=\"fixed-case\">AIDP<\/jats:styled-content> is the commonest variant of <jats:styled-content style=\"fixed-case\">GBS<\/jats:styled-content> in our study and has better outcome compared to <jats:styled-content style=\"fixed-case\">AMAN<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/jns5.12050","type":"journal-article","created":{"date-parts":[[2014,1,23]],"date-time":"2014-01-23T12:13:29Z","timestamp":1390479209000},"page":"36-43","source":"Crossref","is-referenced-by-count":66,"title":["Guillain\u2010Barr\u00e9 syndrome: subtypes and predictors of outcome from India"],"prefix":"10.1111","volume":"19","author":[{"given":"Jayantee","family":"Kalita","sequence":"first","affiliation":[{"name":"Department of Neurology Sanjay Gandhi Post Graduate Institute of Medical Sciences Lucknow India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Usha 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