245 related articles for article (PubMed ID: 17178739)
1. A cryopyrin-associated periodic syndrome with joint destruction.
Lequerré T; Vittecoq O; Saugier-Veber P; Goldenberg A; Patoz P; Frébourg T; Le Loët X
Rheumatology (Oxford); 2007 Apr; 46(4):709-14. PubMed ID: 17178739
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Clinical and genetic characterization of Italian patients affected by CINCA syndrome.
Caroli F; Pontillo A; D'Osualdo A; Travan L; Ceccherini I; Crovella S; Alessio M; Stabile A; Gattorno M; Tommasini A; Martini A; Lepore L
Rheumatology (Oxford); 2007 Mar; 46(3):473-8. PubMed ID: 16920754
[TBL] [Abstract][Full Text] [Related]
4. Positive clinical and biochemical responses to anakinra in a 3-yr-old patient with cryopyrin-associated periodic syndrome (CAPS).
Ramos E; Aróstegui JI; Campuzano S; Rius J; Bousoño C; Yagüe J
Rheumatology (Oxford); 2005 Aug; 44(8):1072-3. PubMed ID: 15840596
[No Abstract] [Full Text] [Related]
5. 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]
6. 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]
7. New CIAS1 mutation and anakinra efficacy in overlapping of Muckle-Wells and familial cold autoinflammatory syndromes.
Maksimovic L; Stirnemann J; Caux F; Ravet N; Rouaghe S; Cuisset L; Letellier E; Grateau G; Morin AS; Fain O
Rheumatology (Oxford); 2008 Mar; 47(3):309-10. PubMed ID: 18174231
[TBL] [Abstract][Full Text] [Related]
8. Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome.
Hentgen V; Despert V; Leprêtre AC; Cuisset L; Chevrant-Breton J; Jégo P; Chalès G; Gall EL; Delpech M; Grateau G
J Rheumatol; 2005 Apr; 32(4):747-51. PubMed ID: 15801036
[TBL] [Abstract][Full Text] [Related]
9. Pattern of interleukin-1beta secretion in response to lipopolysaccharide and ATP before and after interleukin-1 blockade in patients with CIAS1 mutations.
Gattorno M; Tassi S; Carta S; Delfino L; Ferlito F; Pelagatti MA; D'Osualdo A; Buoncompagni A; Alpigiani MG; Alessio M; Martini A; Rubartelli A
Arthritis Rheum; 2007 Sep; 56(9):3138-48. PubMed ID: 17763411
[TBL] [Abstract][Full Text] [Related]
10. A variant Muckle-Wells syndrome with a novel mutation in CIAS1 gene responding to anakinra.
Dalgic B; Egritas O; Sari S; Cuisset L
Pediatr Nephrol; 2007 Sep; 22(9):1391-4. PubMed ID: 17486372
[TBL] [Abstract][Full Text] [Related]
11. Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene.
Aróstegui JI; Aldea A; Modesto C; Rua MJ; Argüelles F; González-Enseñat MA; Ramos E; Rius J; Plaza S; Vives J; Yagüe J
Arthritis Rheum; 2004 Dec; 50(12):4045-50. PubMed ID: 15593220
[TBL] [Abstract][Full Text] [Related]
12. A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian origin.
Shalev SA; Sprecher E; Indelman M; Hujirat Y; Bergman R; Rottem M
Int Arch Allergy Immunol; 2007; 143(3):190-3. PubMed ID: 17284928
[TBL] [Abstract][Full Text] [Related]
13. Long-term efficacy of the interleukin-1 receptor antagonist anakinra in ten patients with neonatal-onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome.
Neven B; Marvillet I; Terrada C; Ferster A; Boddaert N; Couloignier V; Pinto G; Pagnier A; Bodemer C; Bodaghi B; Tardieu M; Prieur AM; Quartier P
Arthritis Rheum; 2010 Jan; 62(1):258-67. PubMed ID: 20039428
[TBL] [Abstract][Full Text] [Related]
14. Nonclassic neurologic features in cryopyrin-associated periodic syndromes.
Ting TV; Scalzi LV; Hashkes PJ
Pediatr Neurol; 2007 May; 36(5):338-41. PubMed ID: 17509468
[TBL] [Abstract][Full Text] [Related]
15. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.
Hoffman HM; Mueller JL; Broide DH; Wanderer AA; Kolodner RD
Nat Genet; 2001 Nov; 29(3):301-5. PubMed ID: 11687797
[TBL] [Abstract][Full Text] [Related]
16. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
Dodé C; Le Dû N; Cuisset L; Letourneur F; Berthelot JM; Vaudour G; Meyrier A; Watts RA; Scott DG; Nicholls A; Granel B; Frances C; Garcier F; Edery P; Boulinguez S; Domergues JP; Delpech M; Grateau G
Am J Hum Genet; 2002 Jun; 70(6):1498-506. PubMed ID: 11992256
[TBL] [Abstract][Full Text] [Related]
17. Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.
Aganna E; Martinon F; Hawkins PN; Ross JB; Swan DC; Booth DR; Lachmann HJ; Bybee A; Gaudet R; Woo P; Feighery C; Cotter FE; Thome M; Hitman GA; Tschopp J; McDermott MF
Arthritis Rheum; 2002 Sep; 46(9):2445-52. PubMed ID: 12355493
[TBL] [Abstract][Full Text] [Related]
18. De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases.
Aksentijevich I; Nowak M; Mallah M; Chae JJ; Watford WT; Hofmann SR; Stein L; Russo R; Goldsmith D; Dent P; Rosenberg HF; Austin F; Remmers EF; Balow JE; Rosenzweig S; Komarow H; Shoham NG; Wood G; Jones J; Mangra N; Carrero H; Adams BS; Moore TL; Schikler K; Hoffman H; Lovell DJ; Lipnick R; Barron K; O'Shea JJ; Kastner DL; Goldbach-Mansky R
Arthritis Rheum; 2002 Dec; 46(12):3340-8. PubMed ID: 12483741
[TBL] [Abstract][Full Text] [Related]
19. Muckle-Wells treatment with anakinra.
Eungdamrong J; Boyd KP; Meehan SA; Latkowski JA
Dermatol Online J; 2013 Dec; 19(12):20720. PubMed ID: 24365011
[TBL] [Abstract][Full Text] [Related]
20. CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes.
Granel B; Philip N; Serratrice J; Ene N; Grateau G; Dodé C; Cuisset L; Disdier P; Berbis P; Delpech M; Weiller PJ
Dermatology; 2003; 206(3):257-9. PubMed ID: 12673085
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
