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Pemphigus has been defined as a group of intractable autoimmune blistering diseases caused by anti\u2010desmoglein 1 and\/or anti\u2010desmoglein 3 IgG autoantibodies by the MHLW. The diagnosis of this condition and the criteria for assessing its severity are based on suggestions from the MHLW Research Group. The clinical practice guidelines presented here are those that are currently recommended in Japan. However, symptoms and complications can vary widely among individual pemphigus patients, so not all therapies will be required to be in complete agreement with these guidelines.<\/jats:p>","DOI":"10.1111\/1346-8138.12486","type":"journal-article","created":{"date-parts":[[2014,6,9]],"date-time":"2014-06-09T11:08:27Z","timestamp":1402312107000},"page":"471-486","source":"Crossref","is-referenced-by-count":76,"title":["Japanese guidelines for the management of pemphigus"],"prefix":"10.1111","volume":"41","author":[{"name":"Committee for Guidelines for the Management of Pemphigus Disease","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masayuki","family":"Amagai","sequence":"additional","affiliation":[{"name":"Department of Dermatology Keio University School of Medicine Tokyo Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Akiko","family":"Tanikawa","sequence":"additional","affiliation":[{"name":"Department of 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