{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,14]],"date-time":"2025-05-14T02:52:22Z","timestamp":1747191142658,"version":"3.40.5"},"reference-count":10,"publisher":"Wiley","license":[{"start":{"date-parts":[[2022,3,4]],"date-time":"2022-03-04T00:00:00Z","timestamp":1646352000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Immunology"],"published-print":{"date-parts":[[2022,3,4]]},"abstract":"<jats:p>Introduction. Anti-SAE1 antibodies have a low prevalence in dermatomyositis patients. Case Description. A 61-year-old woman presented with progressive shortness of breath, arthralgia, heliotrope rash, Gottron\u2019s papules, and erythematous rash. She had an interstitial lung disease (ILD) with a significant decrease in lung function. There was no muscle involvement. Immunological laboratory test results showed strongly positive anti-SAE1 antibodies. Glucocorticoid treatment resulted in remission of dermatomyositis. Conclusion. Anti-SAE antibodies in dermatomyositis patients are closely linked to unique clinical features.<\/jats:p>","DOI":"10.1155\/2022\/9000608","type":"journal-article","created":{"date-parts":[[2022,3,4]],"date-time":"2022-03-04T19:35:07Z","timestamp":1646422507000},"page":"1-4","source":"Crossref","is-referenced-by-count":2,"title":["A Case of Anti-SAE1 Dermatomyositis"],"prefix":"10.1155","volume":"2022","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6719-5119","authenticated-orcid":true,"given":"Max","family":"de Vries","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, Groene Hart Hospital, Bleulandweg 10 2803 HH, Gouda, Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4198-183X","authenticated-orcid":true,"given":"Marco W. 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