Zobrazeno 1 - 10
of 706
pro vyhledávání: '"Cryopyrin-associated periodic syndrome"'
Autor:
Xiaona Zhu, Jiaqi Fan, Yanyan Huang, Yongbin Xu, Zhi Yang, Ruohang Weng, Ying Luo, Jun Yang, Tingyan He
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-9 (2024)
Abstract Objective Cryopyrin-associated periodic syndrome (CAPS) is characterized by excessive IL-1β release resulting in systemic and organ inflammation. As an anti-IL-1 agent, canakinumab has been approved with all CAPS phenotypes in USA and Europ
Externí odkaz:
https://doaj.org/article/1c530000a23649069ebc8f0729c3f6be
Autor:
Zhangwanyu Wei, Zhikun Yang, Donghui Li, Xiao Zhang, Bing Li, Xufeng Zhao, Wenyu Yan, Bingxuan Wu, Na Wu, Xuqian Wang, Weihong Yu, Min Shen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Purpose To determine whether the rare NLRP3-Associated Autoinflammatory Disease (NLRP3-AID) is associated with retinal changes and to assess the ocular involvement. Methods A retrospective cohort study of 20 patients(40 eyes) diagnosed with
Externí odkaz:
https://doaj.org/article/6a805b46f6da453d8daed4371d9eaa8a
Autor:
Mark Yun, Zuoming Deng, Brianne Navetta-Modrov, Baozhong Xin, Jie Yang, Hafsa Nomani, Olga Aroniadis, Peter D. Gorevic, Qingping Yao
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
ObjectivesCryopyrin-associated periodic syndrome or NLRP3-associated autoinflammatory disease (NLRP3-AID) and NLRP12-AID are both Mendelian disorders with autosomal dominant inheritance. Both diseases are rare, primarily reported in the pediatric pop
Externí odkaz:
https://doaj.org/article/3b37f0562fa14d03a02ac1612bfb9dbc
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-8 (2023)
Abstract Background Cryopyrin-associated periodic syndrome (CAPS), a rare genetic autoimmune disease, is composed of familial cold autoinflammatory syndrome (FCAs), Muckle-Wells syndrome (MWS), and neonatal onset multisystem inflammatory disease (NOM
Externí odkaz:
https://doaj.org/article/67aa0da7ed454bcb931d6e9050f4e207
Autor:
Zhou Shu, Yue Zhang, Tongxin Han, Yan Li, Yurong Piao, Fei Sun, Jin Ma, Wenxiu Mo, Jiapeng Sun, Koon-Wing Chan, Wanling Yang, Yu-Lung Lau, Huawei Mao
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Cryopyrin-associated periodic syndrome (CAPS) comprises a group of disorders characterized by recurrent bouts of systemic inflammation related to overactivation of inflammasome. So far, neither large cases of the correlation between genotype and phen
Externí odkaz:
https://doaj.org/article/e15c585946b44e8b8ff9c2b2ae98c543
Publikováno v:
BMC Rheumatology, Vol 6, Iss 1, Pp 1-4 (2022)
Abstract Background NLRP3-associated autoinflammatory diseases (NLRP3-AID) are rare genetic autoinflammatory diseases characterized by chronic inflammation and an urticaria-like rash. We report an unusual presentation of severe NLRP3-AID resulting in
Externí odkaz:
https://doaj.org/article/5d24d7a24f514947a59bd3fb80aa7f4a
Akademický článek
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Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Muckle-Wells syndrome (MWS) is an autosomal dominant autoinflammatory disease recognized as the intermediate phenotype of cryopyrin-associated periodic syndrome (CAPS) caused by NLRP3 gene mutation. It often takes a long time before the diagnosis is
Externí odkaz:
https://doaj.org/article/4f323d73eb5648b4ada096436f09dc97
Akademický článek
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Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The NLRP3 inflammasome is one of the NOD-like receptor family members with the most functional characterization and acts as a key player in innate immune system, participating in several physiological processes including, among others, the modulation
Externí odkaz:
https://doaj.org/article/129fa20220354b8da79fdd87f55285cc