These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
298 related articles for article (PubMed ID: 22146561)
1. NLRP3 E311K mutation in a large family with Muckle-Wells syndrome--description of a heterogeneous phenotype and response to treatment. Kuemmerle-Deschner JB; Lohse P; Koetter I; Dannecker GE; Reess F; Ummenhofer K; Koch S; Tzaribachev N; Bialkowski A; Benseler SM Arthritis Res Ther; 2011; 13(6):R196. PubMed ID: 22146561 [TBL] [Abstract][Full Text] [Related]
2. Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens. Kuemmerle-Deschner JB; Wittkowski H; Tyrrell PN; Koetter I; Lohse P; Ummenhofer K; Reess F; Hansmann S; Koitschev A; Deuter C; Bialkowski A; Foell D; Benseler SM Arthritis Res Ther; 2013; 15(3):R64. PubMed ID: 23718630 [TBL] [Abstract][Full Text] [Related]
3. Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene. Iida Y; Wakiguchi H; Okazaki F; Nakamura T; Yasudo H; Kubo M; Sugahara K; Yamashita H; Suehiro Y; Okayama N; Hashimoto K; Iwamoto N; Kawakami A; Aoki Y; Takada H; Ohga S; Hasegawa S Clin Rheumatol; 2019 Mar; 38(3):943-948. PubMed ID: 30338413 [TBL] [Abstract][Full Text] [Related]
4. Efficacy and safety of anakinra therapy in pediatric and adult patients with the autoinflammatory Muckle-Wells syndrome. Kuemmerle-Deschner JB; Tyrrell PN; Koetter I; Wittkowski H; Bialkowski A; Tzaribachev N; Lohse P; Koitchev A; Deuter C; Foell D; Benseler SM Arthritis Rheum; 2011 Mar; 63(3):840-9. PubMed ID: 21360513 [TBL] [Abstract][Full Text] [Related]
5. A Novel Mutation in the Pyrin Domain of the NOD-like Receptor Family Pyrin Domain Containing Protein 3 in Muckle-Wells Syndrome. Hu J; Zhu Y; Zhang JZ; Zhang RG; Li HM Chin Med J (Engl); 2017 Mar; 130(5):586-593. PubMed ID: 28229991 [TBL] [Abstract][Full Text] [Related]
6. "Mutation negative" familial cold autoinflammatory syndrome (FCAS) in an 8-year-old boy: clinical course and functional studies. Hedrich CM; Bruck N; Paul D; Hahn G; Gahr M; Rösen-Wolff A Rheumatol Int; 2012 Sep; 32(9):2629-36. PubMed ID: 21833523 [TBL] [Abstract][Full Text] [Related]
8. An unusual phenotype in Muckle-Wells syndrome associated with NLRP3 E311K. Murphy G; Daly M; O'Sullivan M; Stack J; Rowczenio D; Lachmann H; Shanahan F; Harney S; Hawkins P; Molloy M Rheumatology (Oxford); 2011 Feb; 50(2):419-20. PubMed ID: 20819795 [No Abstract] [Full Text] [Related]
9. NLRP3 A439V Mutation in a Large Family with Cryopyrin-associated Periodic Syndrome: Description of Ophthalmologic Symptoms in Correlation with Other Organ Symptoms. Sobolewska B; Angermair E; Deuter C; Doycheva D; Kuemmerle-Deschner J; Zierhut M J Rheumatol; 2016 Jun; 43(6):1101-6. PubMed ID: 27134254 [TBL] [Abstract][Full Text] [Related]
10. Audiometric characteristics of a Dutch family with Muckle-Wells syndrome. Weegerink NJ; Schraders M; Leijendeckers J; Slieker K; Huygen PL; Hoefsloot L; Oostrik J; Pennings RJ; Simon A; Snik A; Kremer H; Kunst HP Hear Res; 2011 Dec; 282(1-2):243-51. PubMed ID: 21810457 [TBL] [Abstract][Full Text] [Related]
13. Muckle-Wells syndrome without mutation in exon 3 of the NLRP3 gene, identified by evidence of excessive monocyte production of functional interleukin 1β and rapid response to anakinra. Sabroe RA; Stokes CA; Parker LC; Higgins K; Prince LR; Sabroe I Clin Exp Dermatol; 2013 Dec; 38(8):874-7. PubMed ID: 23889084 [TBL] [Abstract][Full Text] [Related]
14. Resolution of unilateral sensorineural hearing loss in a pediatric patient with a severe phenotype of Muckle-Wells syndrome treated with Anakinra: a case report and review of the literature. Marchica C; Zawawi F; Basodan D; Scuccimarri R; Daniel SJ J Otolaryngol Head Neck Surg; 2018 Jan; 47(1):9. PubMed ID: 29382382 [TBL] [Abstract][Full Text] [Related]
15. Muckle-Wells Syndrome: A Case Report with an NLRP3 T348M Mutation. Naz Villalba E; Gomez de la Fuente E; Caro Gutierrez D; Pinedo Moraleda F; Yanguela Rodilla J; Mazagatos Angulo D; López Estebaranz JL Pediatr Dermatol; 2016 Sep; 33(5):e311-4. PubMed ID: 27435956 [TBL] [Abstract][Full Text] [Related]
16. Early detection of sensorineural hearing loss in Muckle-Wells-syndrome. Kuemmerle-Deschner JB; Koitschev A; Tyrrell PN; Plontke SK; Deschner N; Hansmann S; Ummenhofer K; Lohse P; Koitschev C; Benseler SM Pediatr Rheumatol Online J; 2015 Nov; 13(1):43. PubMed ID: 26531310 [TBL] [Abstract][Full Text] [Related]
17. MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes. Wittkowski H; Kuemmerle-Deschner JB; Austermann J; Holzinger D; Goldbach-Mansky R; Gramlich K; Lohse P; Jung T; Roth J; Benseler SM; Foell D Ann Rheum Dis; 2011 Dec; 70(12):2075-2081. PubMed ID: 21908452 [TBL] [Abstract][Full Text] [Related]
18. Anakinra improves sensory deafness in a Japanese patient with Muckle-Wells syndrome, possibly by inhibiting the cryopyrin inflammasome. Yamazaki T; Masumoto J; Agematsu K; Sawai N; Kobayashi S; Shigemura T; Yasui K; Koike K Arthritis Rheum; 2008 Mar; 58(3):864-8. PubMed ID: 18311804 [TBL] [Abstract][Full Text] [Related]
19. Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra. Hawkins PN; Lachmann HJ; Aganna E; McDermott MF Arthritis Rheum; 2004 Feb; 50(2):607-12. PubMed ID: 14872505 [TBL] [Abstract][Full Text] [Related]