Zobrazeno 1 - 10
of 1 736
pro vyhledávání: '"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:
Risha, Basma E.-S.1 dr.basmaelsayed@yahoo.com, Al-Aziz, Ghada A.1, Ahmed, Naglaa S.2, Hamdino, Mervat1
Publikováno v:
Scientific Journal of Al-Azhar Medical Faculty, Girls. Oct-Dec2020, Vol. 4 Issue 4, p586-593. 8p.
Autor:
Gattorno, Marco, Obici, Laura, Penadés, Inmaculada Calvo, Kallinich, Tilmann, Benseler, Susanne, Dekker, Elise, Lévy, Jérémy, De Benedetti, Fabrizio, Lachmann, Helen
Publikováno v:
Arthritis & Rheumatology; Feb2024, Vol. 76 Issue 2, p304-312, 9p
Autor:
Mengqing Qian, Jingyu Zhou, Jing Wu, Haocheng Zhang, Shenglei Yu, Haoxin Xu, Yixuan Yang, Feiran Zhou, Qingluan Yang, Lingyun Shao, Wenhong Zhang, Ning Jiang, Qiaoling Ruan
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
BackgroundTumor necrosis factor receptor-associated periodic syndrome (TRAPS) is a rare autosomal dominant disorder with a low incidence in Asia. The most frequent clinical manifestations include fever, rash, myalgia, joint pain and abdominal pain. M
Externí odkaz:
https://doaj.org/article/b972310d6c744844a101dfbd52325764
Autor:
Yandie Li, Meiping Lu
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-10 (2024)
Abstract Background Mevalonate kinase deficiency (MKD) and TNF receptor-associated periodic syndrome (TRAPS) are categorized as systemic autoinflammatory diseases (SAIDs), which are rare diseases characterized by early onset, severe conditions, and c
Externí odkaz:
https://doaj.org/article/a6d9d4a97fd44f7d8b5826ef181a48f9
Autor:
Grandemange, Sylvie1,2 sylvie.grandemange@inserm.fr, Cabasson, Sébastien3, Sarrabay, Guillaume1,2,4,5, Pène, Jérôme2, Rittore, Cécile1,2, Sanchez, Elodie1,2, Chastang, Marie‐Caroline6, Guyon, Gaël7, Pillet, Pascal6, Touitou, Isabelle1,2,4,5
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2017, Vol. 5 Issue 2, p110-116. 7p.
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
Publikováno v:
Life, Vol 14, Iss 6, p 717 (2024)
Background: The purpose of this review is to clarify the natural course of benign paroxysmal torticollis (BPT) and update the information on the relationship of this disorder with migraine. BPT belongs to a group of “episodic syndromes that may be
Externí odkaz:
https://doaj.org/article/dda452d7e7ec4dc2a8a3959cbcdcf730
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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