{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,8]],"date-time":"2025-10-08T15:43:49Z","timestamp":1759938229193},"reference-count":11,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2007,5,6]],"date-time":"2007-05-06T00:00:00Z","timestamp":1178409600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ther Apher Dial"],"published-print":{"date-parts":[[2007,6]]},"abstract":"<jats:p><jats:bold>Abstract:\u2002<\/jats:bold> Neonatal onset multisystem inflammatory disease (NOMID), which is also known as chronic infantile neurological cutaneous and articular syndrome, is a rare disease that is characterized by the triad of cutaneous rash, chronic meningitis and arthropathy. The long\u2010term prognosis is poor, with progressive deafness and visual impairment, and worsening of the central nervous system manifestations. Some fatal cases have been reported secondary to infection, vasculitis and amyloidosis. We recently managed a typical case of NOMID where the combined treatment of continuous hemodiafiltration and steroid pulse therapy was effective. The patient showed repeated flare ups of fever, arthralgia and meningitis accompanied with high levels of cytokines. The effect was temporary, but useful in recovery from such a serious condition.<\/jats:p>","DOI":"10.1111\/j.1744-9987.2007.00465.x","type":"journal-article","created":{"date-parts":[[2007,5,9]],"date-time":"2007-05-09T21:22:51Z","timestamp":1178745771000},"page":"232-234","source":"Crossref","is-referenced-by-count":5,"title":["A Case Report of Neonatal Onset Multisystemic Inflammatory Disease in Japan Treated With Continuous Hemodiafiltration and Steroid Pulse Therapy"],"prefix":"10.1111","volume":"11","author":[{"given":"Hisashi","family":"Kawashima","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akiko","family":"Sato","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shigeo","family":"Nishimata","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Naoto","family":"Yamada","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasuyo","family":"Kashiwagi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kiyoko","family":"Watanabe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kouji","family":"Takekuma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akinori","family":"Hoshika","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takurou","family":"Ozawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2007,5,6]]},"reference":[{"key":"e_1_2_4_2_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00361425"},{"key":"e_1_2_4_3_2","first-page":"1070","article-title":"Syndrome for diagnosis: dwarfing, persistently open fontanelle; recurrent meningitis; recurrent subdural effusions with temporary alternate\u2010sided hemiplegia; high\u2010tone deafness; visual defect with pseudopapilledema; slowing intellectual development; recurrent acute polyarthritis; erythema marginatum, splenomegaly and iron\u2010resistant hypochromic anaemia","volume":"66","author":"Lorber J","year":"1973","journal-title":"Proc R Soc Med"},{"key":"e_1_2_4_4_2","first-page":"103","article-title":"A recently recognized chronic inflammatory disease of early onset characterized by the triad of rash, central nervous system involvement and arthropathy","volume":"19","author":"Prieur AM","year":"2001","journal-title":"Clin Exp Rheumatol"},{"key":"e_1_2_4_5_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2003-07-2531"},{"key":"e_1_2_4_6_2","doi-asserted-by":"publisher","DOI":"10.1002\/art.10688"},{"key":"e_1_2_4_7_2","doi-asserted-by":"publisher","DOI":"10.1093\/rheumatology\/kel269"},{"key":"e_1_2_4_8_2","doi-asserted-by":"publisher","DOI":"10.1080\/03009740410010236"},{"key":"e_1_2_4_9_2","doi-asserted-by":"publisher","DOI":"10.1002\/art.20953"},{"key":"e_1_2_4_10_2","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.141.2.248"},{"key":"e_1_2_4_11_2","doi-asserted-by":"publisher","DOI":"10.1038\/nm1201-1291"},{"key":"e_1_2_4_12_2","doi-asserted-by":"publisher","DOI":"10.1046\/j.1526-0968.2002.00464.x"}],"container-title":["Therapeutic Apheresis and Dialysis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1744-9987.2007.00465.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1744-9987.2007.00465.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,14]],"date-time":"2023-10-14T04:17:46Z","timestamp":1697257066000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1744-9987.2007.00465.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,5,6]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2007,6]]}},"alternative-id":["10.1111\/j.1744-9987.2007.00465.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1744-9987.2007.00465.x","archive":["Portico"],"relation":{},"ISSN":["1744-9979","1744-9987"],"issn-type":[{"value":"1744-9979","type":"print"},{"value":"1744-9987","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,5,6]]}}}