{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T13:41:31Z","timestamp":1777902091609,"version":"3.51.4"},"reference-count":18,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Science Progress"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:p>Guillain\u2013Barr\u00e9 syndrome (GBS) is a life-threatening acute paralytic neuropathy characterized by rapidly progressive limb weakness and bilateral cranial nerve involvement. We report an early 70s male with no relevant medical history diagnosed with anti-GM3 IgG-positive GBS, who developed unilateral oculomotor nerve palsy and autonomic dysfunction during intravenous immunoglobulin (IVIG) therapy, with spontaneous symptom resolution following IVIG completion. Six-month follow-up assessments confirmed complete remission. This case reinforces the therapeutic value of IVIG in GBS patients with specific autoantibody profiles, even when complicated by transient neurological deterioration during treatment.<\/jats:p>","DOI":"10.1177\/00368504251406582","type":"journal-article","created":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T18:23:37Z","timestamp":1768415017000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Guillain\u2013Barr\u00e9 syndrome with unilateral oculomotor nerve palsy and anti-GM3 IgG antibodies"],"prefix":"10.1177","volume":"109","author":[{"given":"Minjia","family":"Xiao","sequence":"first","affiliation":[{"name":"Department of Neurology, Yueyang Central Hospital, Yueyang City, Hunan Province, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiang","family":"Huang","sequence":"additional","affiliation":[{"name":"Department of Neurology, Yueyang Central Hospital, Yueyang City, Hunan Province, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2026,1,14]]},"reference":[{"key":"e_1_3_3_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(21)00517-1"},{"key":"e_1_3_3_3_2","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/awn074"},{"key":"e_1_3_3_4_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.43.10.1911"},{"key":"e_1_3_3_5_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(16)00339-1"},{"key":"e_1_3_3_6_2","doi-asserted-by":"publisher","DOI":"10.1136\/thx.54.7.581"},{"key":"e_1_3_3_7_2","doi-asserted-by":"publisher","DOI":"10.1111\/head.12246"},{"key":"e_1_3_3_8_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.mayocp.2016.12.002"},{"key":"e_1_3_3_9_2","doi-asserted-by":"publisher","DOI":"10.1007\/s10072-018-3283-8"},{"key":"e_1_3_3_10_2","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-008-0775-0"},{"key":"e_1_3_3_11_2","doi-asserted-by":"publisher","DOI":"10.1096\/fj.05-4911fje"},{"key":"e_1_3_3_12_2","doi-asserted-by":"publisher","DOI":"10.4103\/0028-3886.86549"},{"key":"e_1_3_3_13_2","doi-asserted-by":"publisher","DOI":"10.1002\/mus.25266"},{"key":"e_1_3_3_14_2","first-page":"15","article-title":"A rare presentation of acute-onset chronic inflammatory demyelinating polyneuropathy with the detection of anti-GM3 and anti-sulfatides antibodies: a case report","author":"Sun R","year":"2024","unstructured":"Sun R, Meng Y, Li L, et al. A rare presentation of acute-onset chronic inflammatory demyelinating polyneuropathy with the detection of anti-GM3 and anti-sulfatides antibodies: a case report. Front Immunol 2024: 15: 1409637.","journal-title":"Front Immunol"},{"key":"e_1_3_3_15_2","first-page":"78","article-title":"Autoimmune glial fibrillary acidic protein astrocytopathy with the detection of anti-GM3 and anti-GM4 IgG antibodies, masquerading as Brown\u2013S\u00e9quard syndrome","author":"Zhou Z-H","year":"2021","unstructured":"Zhou Z-H, Yu Q-Y, Hong M-F. Autoimmune glial fibrillary acidic protein astrocytopathy with the detection of anti-GM3 and anti-GM4 IgG antibodies, masquerading as Brown\u2013S\u00e9quard syndrome. 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