108 related articles for article (PubMed ID: 16871551)
1. Mutational analysis in neonatal-onset multisystem inflammatory disease: comment on the articles by Frenkel et al and Saito et al.
Aksentijevich I; Remmers EF; Goldbach-Mansky R; Reiff A; Kastner DL
Arthritis Rheum; 2006 Aug; 54(8):2703-4; author reply 2704-5. PubMed ID: 16871551
[No Abstract] [Full Text] [Related]
2. Neonatal-onset multisystem inflammatory disorder: the emerging role of pyrin genes in autoinflammatory diseases.
Kilcline C; Shinkai K; Bree A; Modica R; Von Scheven E; Frieden IJ
Arch Dermatol; 2005 Feb; 141(2):248-53. PubMed ID: 15724022
[TBL] [Abstract][Full Text] [Related]
3. Cryopyrin-associated periodic syndromes and autoinflammation.
Shinkai K; McCalmont TH; Leslie KS
Clin Exp Dermatol; 2008 Jan; 33(1):1-9. PubMed ID: 17927785
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of the CIAS1 gene and response to interleukin-1 receptor antagonist treatment.
Boschan C; Witt O; Lohse P; Foeldvari I; Zappel H; Schweigerer L
Am J Med Genet A; 2006 Apr; 140(8):883-6. PubMed ID: 16532456
[TBL] [Abstract][Full Text] [Related]
6. Anakinra in mutation-negative NOMID/CINCA syndrome: comment on the articles by Hawkins et al and Hoffman and Patel.
Frenkel J; Wulffraat NM; Kuis W
Arthritis Rheum; 2004 Nov; 50(11):3738-9; author reply 3739-40. PubMed ID: 15529342
[No Abstract] [Full Text] [Related]
7. A CIAS1 mutation in a Japanese girl with familial cold autoinflammatory syndrome.
Kanegane H; Itazawa T; Saito M; Nishikomori R; Makino T; Shimizu T; Adachi Y; Nakahata T; Miyawaki T
Eur J Pediatr; 2008 Feb; 167(2):245-7. PubMed ID: 17333269
[No Abstract] [Full Text] [Related]
8. Somatic mosaicism of CIAS1 in a patient with chronic infantile neurologic, cutaneous, articular syndrome.
Saito M; Fujisawa A; Nishikomori R; Kambe N; Nakata-Hizume M; Yoshimoto M; Ohmori K; Okafuji I; Yoshioka T; Kusunoki T; Miyachi Y; Heike T; Nakahata T
Arthritis Rheum; 2005 Nov; 52(11):3579-85. PubMed ID: 16255047
[TBL] [Abstract][Full Text] [Related]
9. Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndrome.
Pörksen G; Lohse P; Rösen-Wolff A; Heyden S; Förster T; Wendisch J; Heubner G; Bernuth H; Sallmann S; Gahr M; Roesler J
Eur J Haematol; 2004 Aug; 73(2):123-7. PubMed ID: 15245511
[TBL] [Abstract][Full Text] [Related]
10. A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapy.
Stojanov S; Weiss M; Lohse P; Belohradsky BH
Pediatrics; 2004 Jul; 114(1):e124-7. PubMed ID: 15231984
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. A fever gene comes in from the cold.
Kastner DL; O'Shea JJ
Nat Genet; 2001 Nov; 29(3):241-2. PubMed ID: 11687785
[No Abstract] [Full Text] [Related]
14. A case of Muckle-Wells syndrome caused by a novel H312P mutation in NALP3 (cryopyrin).
Koike R; Kubota T; Hara Y; Ito S; Suzuki K; Yanagisawa K; Uchibori K; Miyasaka N
Mod Rheumatol; 2007; 17(6):496-9. PubMed ID: 18084703
[TBL] [Abstract][Full Text] [Related]
15. A case of familial cold autoinflammatory syndrome confirmed by the presence of a CIAS1 mutation.
Shpall RL; Jeffes EW; Hoffman HM
Br J Dermatol; 2004 May; 150(5):1029-31. PubMed ID: 15149524
[No Abstract] [Full Text] [Related]
16. The PYRIN connection: novel players in innate immunity and inflammation.
Stehlik C; Reed JC
J Exp Med; 2004 Sep; 200(5):551-8. PubMed ID: 15353551
[TBL] [Abstract][Full Text] [Related]
17. Inherited autoinflammatory recurrent fevers.
Pradalier A; Cauvain A; Oukachbi Z
Eur Ann Allergy Clin Immunol; 2006 Jan; 38(1):5-9. PubMed ID: 16544581
[TBL] [Abstract][Full Text] [Related]
18. Mutations in cryopyrin: bypassing roadblocks in the caspase 1 inflammasome for interleukin-1beta secretion and disease activity.
Dinarello CA
Arthritis Rheum; 2007 Sep; 56(9):2817-22. PubMed ID: 17763412
[No Abstract] [Full Text] [Related]
19. A fatal Turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation.
Gunduz Z; Dursun I; Aróstegui JI; Yagüe J; Dusunsel R; Poyrazoglu HM; Gurgoze MK; Yikilmaz A
Rheumatol Int; 2008 Feb; 28(4):379-83. PubMed ID: 17684747
[No Abstract] [Full Text] [Related]
20. [Description of a case of hyperkinetic movement disorder in neonatal onset multisystem inflammatory disease or chronic infantile neurologic cutaneous and articular syndrome].
Gómez-Camello Á; Ortego-Centeno N
Rev Neurol; 2014 Jan; 58(2):94-6. PubMed ID: 24399627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
