184 related articles for article (PubMed ID: 28028683)
1. Muckle-Wells syndrome in Chinese patients: a single center case series.
Wu D; Shen M
Clin Rheumatol; 2017 Apr; 36(4):965-969. PubMed ID: 28028683
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The phenotype and genotype of Chinese adult patients with NLRP3-associated autoinflammatory disease.
Wu N; Wu D; Miao J; Zhao M; Wang Y; Yu W; Shen M
Clin Rheumatol; 2023 Oct; 42(10):2841-2848. PubMed ID: 37368056
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry.
Levy R; Gérard L; Kuemmerle-Deschner J; Lachmann HJ; Koné-Paut I; Cantarini L; Woo P; Naselli A; Bader-Meunier B; Insalaco A; Al-Mayouf SM; Ozen S; Hofer M; Frenkel J; Modesto C; Nikishina I; Schwarz T; Martino S; Meini A; Quartier P; Martini A; Ruperto N; Neven B; Gattorno M;
Ann Rheum Dis; 2015 Nov; 74(11):2043-9. PubMed ID: 25038238
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation.
Abdulla MC; Alungal J; Hawkins PN; Mohammed S
J Postgrad Med; 2015; 61(2):120-2. PubMed ID: 25766347
[TBL] [Abstract][Full Text] [Related]
9. Hearing loss in Muckle-Wells syndrome.
Kuemmerle-Deschner JB; Koitschev A; Ummenhofer K; Hansmann S; Plontke SK; Koitschev C; Koetter I; Angermair E; Benseler SM
Arthritis Rheum; 2013 Mar; 65(3):824-31. PubMed ID: 23440695
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes.
Nakagawa K; Gonzalez-Roca E; Souto A; Kawai T; Umebayashi H; Campistol JM; Cañellas J; Takei S; Kobayashi N; Callejas-Rubio JL; Ortego-Centeno N; Ruiz-Ortiz E; Rius F; Anton J; Iglesias E; Jimenez-Treviño S; Vargas C; Fernandez-Martin J; Calvo I; Hernández-Rodríguez J; Mendez M; Dordal MT; Basagaña M; Bujan S; Yashiro M; Kubota T; Koike R; Akuta N; Shimoyama K; Iwata N; Saito MK; Ohara O; Kambe N; Yasumi T; Izawa K; Kawai T; Heike T; Yagüe J; Nishikomori R; Aróstegui JI
Ann Rheum Dis; 2015 Mar; 74(3):603-10. PubMed ID: 24326009
[TBL] [Abstract][Full Text] [Related]
12. Identification of a variant in NLRP3 gene in a patient with Muckle-Wells syndrome: a case report and review of literature.
Liu J; Zhang R; Yi Z; Lin Y; Chang H; Zhang Q
Pediatr Rheumatol Online J; 2023 Feb; 21(1):15. PubMed ID: 36765385
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic and genotypic characterization of Chinese adult patients with NLRP3-associated autoinflammatory disease with hearing loss.
Wu B; Luo Y; Wu D; Wang Y; Shen M
Rheumatology (Oxford); 2024 May; 63(6):1690-1698. PubMed ID: 37656934
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Evaluation of common NLRP3 Q703K variant in pediatric patients with autoinflammatory disease: CAPS and PFAPA.
Kendir-Demirkol Y; Jenny LA; Demir F; Sözeri B
Turk J Pediatr; 2023; 65(4):650-660. PubMed ID: 37661680
[TBL] [Abstract][Full Text] [Related]
16. Increased Prevalence of
Theodoropoulou K; Wittkowski H; Busso N; Von Scheven-Gête A; Moix I; Vanoni F; Hengten V; Horneff G; Haas JP; Fischer N; Palm-Beden K; Berendes R; Heubner G; Jansson A; Lainka E; Leimgruber A; Morris M; Foell D; Hofer M
Front Immunol; 2020; 11():877. PubMed ID: 32477355
[No Abstract] [Full Text] [Related]
17. Risk factors for severe Muckle-Wells syndrome.
Kümmerle-Deschner JB; Tyrrell PN; Reess F; Kötter I; Lohse P; Girschick H; Huemer C; Horneff G; Haas JP; Koitschev A; Deuter C; Benseler SM
Arthritis Rheum; 2010 Dec; 62(12):3783-91. PubMed ID: 20722029
[TBL] [Abstract][Full Text] [Related]
18. [Renal amyloidosis revealing a cryopyrin associated periodic syndrome].
Robinet G; Renaudineau E; Lamaison C; Cam G; Rioux-Leclercq N
Ann Pathol; 2018 Dec; 38(6):401-406. PubMed ID: 30236822
[TBL] [Abstract][Full Text] [Related]
19. Muckle-Wells Syndrome Across Four Generations in One Czech Family: Natural Course of the Disease.
Fingerhutová Š; Fráňová J; Hlaváčková E; Jančová E; Procházková L; Beránková K; Tesařová M; Honsová E; Doležalová P
Front Immunol; 2019; 10():802. PubMed ID: 31057541
[No Abstract] [Full Text] [Related]
20. Diagnosis of cryopyrin-associated periodic syndrome: challenges, recommendations and emerging concepts.
Sarrabay G; Grandemange S; Touitou I
Expert Rev Clin Immunol; 2015; 11(7):827-35. PubMed ID: 25979514
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
