{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1390282679852270592.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.2169/internalmedicine.55.6262"}},{"identifier":{"@type":"PMID","@value":"27432103"}},{"identifier":{"@type":"URI","@value":"https://www.jstage.jst.go.jp/article/internalmedicine/55/14/55_55.6262/_pdf"}},{"identifier":{"@type":"NAID","@value":"130005164995"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@language":"en","@value":"Overlap of Myasthenia Gravis and Miller Fisher Syndrome"}],"dc:language":"en","description":[{"type":"abstract","notation":[{"@language":"en","@value":"<p>In this case report, we describe a patient with myasthenia gravis (MG) and Miller Fisher syndrome (MFS) overlap. A 69-year-old woman presented with acute bilateral ptosis, ophthalmoplegia, ataxic gait, and areflexia. The MFS diagnosis was confirmed with by a positive anti-GQ1b IgG antibody test result. MG was diagnosed from electrophysiological, edrophonium, and serological test results. Although intravenous immunoglobulin therapy is effective for both diseases, two courses of the therapy did not improve the patient's symptoms. However, steroid therapy was effective. Although the overlap of MG and MFS is very rare, it should be considered in the differential diagnosis of neuro-ophthalmic diseases. </p>"}],"abstractLicenseFlag":"disallow"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1410001204870588801","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000014116206"},{"@type":"NRID","@value":"9000365523957"},{"@type":"NRID","@value":"9000014025340"},{"@type":"NRID","@value":"9000021702332"},{"@type":"NRID","@value":"9000365523918"},{"@type":"NRID","@value":"9000288799178"},{"@type":"NRID","@value":"9000013877885"},{"@type":"NRID","@value":"9000022057818"},{"@type":"NRID","@value":"9000252876665"},{"@type":"NRID","@value":"9000256346231"},{"@type":"NRID","@value":"9000327927732"},{"@type":"NRID","@value":"9000288799161"},{"@type":"NRID","@value":"9000018209396"},{"@type":"NRID","@value":"9000389964524"},{"@type":"NRID","@value":"9000399564356"},{"@type":"NRID","@value":"9000327927846"},{"@type":"NRID","@value":"9000020580988"},{"@type":"NRID","@value":"9000365523941"},{"@type":"NRID","@value":"9000399169310"},{"@type":"NRID","@value":"9000242154359"},{"@type":"NRID","@value":"9000402903108"},{"@type":"NRID","@value":"9000345220049"},{"@type":"NRID","@value":"9000412266645"},{"@type":"NRID","@value":"9000389964541"},{"@type":"NRID","@value":"9000406033188"},{"@type":"NRID","@value":"9000000756297"},{"@type":"NRID","@value":"9000020274785"},{"@type":"NRID","@value":"9000258213606"},{"@type":"NRID","@value":"9000365523907"},{"@type":"NRID","@value":"9000020169839"},{"@type":"NRID","@value":"9000021325325"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read0152895"}],"foaf:name":[{"@language":"en","@value":"Tanaka Yuji"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Neurology, Gifu Municipal Hospital, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1410282679852270593","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000327927733"}],"foaf:name":[{"@language":"en","@value":"Satomi Kazuo"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Neurology, Gifu Municipal Hospital, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"09182918"},{"@type":"EISSN","@value":"13497235"}],"prism:publicationName":[{"@language":"en","@value":"Internal Medicine"},{"@language":"en","@value":"Intern. Med."}],"dc:publisher":[{"@language":"en","@value":"The Japanese Society of Internal Medicine"},{"@language":"ja","@value":"一般社団法人 日本内科学会"}],"prism:publicationDate":"2016","prism:volume":"55","prism:number":"14","prism:startingPage":"1917","prism:endingPage":"1918"},"reviewed":"false","dcterms:accessRights":"http://purl.org/coar/access_right/c_abf2","url":[{"@id":"https://www.jstage.jst.go.jp/article/internalmedicine/55/14/55_55.6262/_pdf"}],"availableAt":"2016","foaf:topic":[{"@id":"https://cir.nii.ac.jp/all?q=myasthenia%20gravis","dc:title":"myasthenia gravis"},{"@id":"https://cir.nii.ac.jp/all?q=Miller%20Fisher%20syndrome","dc:title":"Miller Fisher syndrome"},{"@id":"https://cir.nii.ac.jp/all?q=anti-acetylcholine%20receptor%20antibody","dc:title":"anti-acetylcholine receptor antibody"},{"@id":"https://cir.nii.ac.jp/all?q=anti-GQ1b%20IgG%20antibody","dc:title":"anti-GQ1b IgG antibody"},{"@id":"https://cir.nii.ac.jp/all?q=overlap%20syndrome","dc:title":"overlap syndrome"}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360574096495588608","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The co-occurrence of serologically proven myasthenia gravis and Miller Fisher/Guillain Barré overlap syndrome — A case report"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570378700544","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Temporal coincidence between AMAN type of GBS and myasthenia gravis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137046540778240","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A case of ocular myasthenia gravis and Miller-Fisher syndrome"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520100359168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Neuromuscular Junction Dysfunction in Miller Fisher Syndrome"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993664001408","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Temporal coincidence of myasthenia gravis and Guillain Barré syndrome associated with Hashimoto thyroiditis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470867967616","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"IgG from patients with Guillain–Barré syndrome interact with nicotinic acetylcholine receptor channels"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421078082432","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Myasthenia gravis: clinical, immunological, and therapeutic advances"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388845324754944","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Combined Guillain–Barré syndrome and myasthenia gravis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319810841984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Guillain-Barré syndrome"}]},{"@id":"https://cir.nii.ac.jp/crid/1390564238101315840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"A case of Miller Fisher syndrome with a false-positive edrophonium test"},{"@language":"ja","@value":"エドロホニウムテスト偽陽性であったMiller Fisher症候群の1例"}]},{"@id":"https://cir.nii.ac.jp/crid/1520573331040378240","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"CLINICAL INVESTIGATION : Clinical features and treatment status of antiacetylcholine receptor antibody-positive ocular myasthenia gravis"}]}],"dataSourceIdentifier":[{"@type":"JALC","@value":"oai:japanlinkcenter.org:2001041398"},{"@type":"CROSSREF","@value":"10.2169/internalmedicine.55.6262"},{"@type":"PUBMED","@value":"27432103"},{"@type":"CIA","@value":"130005164995"},{"@type":"OPENAIRE","@value":"doi_dedup___::66502ccddf07213284721d7c9ee22820"},{"@type":"CROSSREF","@value":"10.5692/clinicalneurol.cn-001236_references_DOI_TDhJKGcWxAlhKns2gLVI6h3Y7DX"},{"@type":"CROSSREF","@value":"10.1007/s10384-020-00770-z_references_DOI_TDhJKGcWxAlhKns2gLVI6h3Y7DX"}]}