Muckle–Wells syndrome: manifestations and diagnosis in four generations of a Portuguese family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12519-020-00358-0.pdf
Reference5 articles.
1. Muzumdar S, Rothe MJ, Grant-Kels JM. The rash with maculopapules and fever in children. Clin Dermatol. 2019;37:119–28.
2. Sobolewska B, Angermair E, Deuter C, Doycheva D, Kuemmerle-Deschner J, Zierhut M. NLRP3 A439V mutation in a large family with cryopyrin-associated periodic syndrome: description of ophthalmologic symptoms in correlation with other organ symptoms. J Rheumatol. 2016;43:1101–6.
3. Muckle TJ, Wells M. Urticaria, deafness, and amyloidosis: a new heredofamilial syndrome. Q J Med. 1962;31:235–48.
4. Ciccarelli F, De Martinis M, Ginaldi L. An update on autoinflammatory diseases. Curr Med Chem. 2014;21:261–9.
5. Tran TA. Muckle–Wells syndrome: clinical perspectives. Br J Nurs. 2019;28:1180–6.
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1. NLRP3 inflammasome and NLRP3-related autoinflammatory diseases: From cryopyrin function to targeted therapies;Frontiers in Immunology;2022-10-06
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