291 related articles for article (PubMed ID: 17213252)
1. Autoinflammatory gene mutations in Behçet's disease.
Koné-Paut I; Sanchez E; Le Quellec A; Manna R; Touitou I
Ann Rheum Dis; 2007 Jun; 66(6):832-4. PubMed ID: 17213252
[TBL] [Abstract][Full Text] [Related]
2. Mevalonate kinase gene mutations and their clinical correlations in Behçet's disease.
Arslan Taş D; Erken E; Yildiz F; Dinkçi S; Sakalli H
Int J Rheum Dis; 2014 May; 17(4):435-43. PubMed ID: 24411001
[TBL] [Abstract][Full Text] [Related]
3. Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.
Burillo-Sanz S; Montes-Cano MA; García-Lozano JR; Ortiz-Fernández L; Ortego-Centeno N; García-Hernández FJ; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Rosa Juliá M; Solans R; Blanco R; Barnosi-Marín AC; Gómez De la Torre R; Fanlo P; Rodríguez-Carballeira M; Rodríguez-Rodríguez L; Camps T; Castañeda S; Alegre-Sancho JJ; Martín J; González-Escribano MF
Sci Rep; 2017 Aug; 7(1):8453. PubMed ID: 28814775
[TBL] [Abstract][Full Text] [Related]
4. The Relationship between NALP3 and Autoinflammatory Syndromes.
Campbell L; Raheem I; Malemud CJ; Askari AD
Int J Mol Sci; 2016 May; 17(5):. PubMed ID: 27187378
[TBL] [Abstract][Full Text] [Related]
5. A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome.
Kutukculer N; Gulez N; Karaca N; Aksu G; Berdeli A
Int J Immunogenet; 2010 Feb; 37(1):21-5. PubMed ID: 19804406
[TBL] [Abstract][Full Text] [Related]
6. Behçet's disease and hereditary periodic fever syndromes: casual association or causal relationship?
Espinosa G; Arostegui JI; Plaza S; Rius J; Cervera R; Yagüe J; Font J
Clin Exp Rheumatol; 2005; 23(4 Suppl 38):S64-6. PubMed ID: 16273767
[TBL] [Abstract][Full Text] [Related]
7. Identification of a homozygous PSTPIP1 mutation in a patient with a PAPA-like syndrome responding to canakinumab treatment.
Geusau A; Mothes-Luksch N; Nahavandi H; Pickl WF; Wise CA; Pourpak Z; Ponweiser E; Eckhart L; Sunder-Plassmann R
JAMA Dermatol; 2013 Feb; 149(2):209-15. PubMed ID: 23426477
[TBL] [Abstract][Full Text] [Related]
8. Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases.
Holzinger D; Fassl SK; de Jager W; Lohse P; Röhrig UF; Gattorno M; Omenetti A; Chiesa S; Schena F; Austermann J; Vogl T; Kuhns DB; Holland SM; Rodríguez-Gallego C; López-Almaraz R; Arostegui JI; Colino E; Roldan R; Fessatou S; Isidor B; Poignant S; Ito K; Epple HJ; Bernstein JA; Jeng M; Frankovich J; Lionetti G; Church JA; Ong PY; LaPlant M; Abinun M; Skinner R; Bigley V; Sachs UJ; Hinze C; Hoppenreijs E; Ehrchen J; Foell D; Chae JJ; Ombrello A; Aksentijevich I; Sunderkoetter C; Roth J
J Allergy Clin Immunol; 2015 Nov; 136(5):1337-45. PubMed ID: 26025129
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
Özkılınç Önen M; Onat UI; Uğurlu S; Timuçin AC; Öz Arslan D; Everest E; Özdoğan H; Tahir Turanlı E
Rheumatology (Oxford); 2023 Sep; 62(9):3188-3196. PubMed ID: 36692132
[TBL] [Abstract][Full Text] [Related]
11. Diagnosis and management of autoinflammatory diseases in childhood.
Gattorno M; Federici S; Pelagatti MA; Caorsi R; Brisca G; Malattia C; Martini A
J Clin Immunol; 2008 May; 28 Suppl 1():S73-83. PubMed ID: 18368292
[TBL] [Abstract][Full Text] [Related]
12. MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever.
D'Osualdo A; Picco P; Caroli F; Gattorno M; Giacchino R; Fortini P; Corona F; Tommasini A; Salvi G; Specchia F; Obici L; Meini A; Ricci A; Seri M; Ravazzolo R; Martini A; Ceccherini I
Eur J Hum Genet; 2005 Mar; 13(3):314-20. PubMed ID: 15536479
[TBL] [Abstract][Full Text] [Related]
13. Novel PSTPIP1 gene mutation in a patient with pyogenic arthritis, pyoderma gangrenosum and acne (PAPA) syndrome.
Lindwall E; Singla S; Davis WE; Quinet RJ
Semin Arthritis Rheum; 2015 Aug; 45(1):91-3. PubMed ID: 25845478
[TBL] [Abstract][Full Text] [Related]
14. Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes.
Burillo-Sanz S; Montes-Cano MA; García-Lozano JR; Olivas-Martínez I; Ortego-Centeno N; García-Hernández FJ; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Juliá MR; Solans R; Blanco R; Barnosi-Marín AC; Gómez de la Torre R; Fanlo P; Rodríguez-Carballeira M; Rodríguez-Rodríguez L; Camps T; Castañeda S; Alegre-Sancho JJ; Martín J; González-Escribano MF
Sci Rep; 2019 Feb; 9(1):2777. PubMed ID: 30808881
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the PSTPIP1 gene and aberrant splicing variants in patients with pyoderma gangrenosum.
Nesterovitch AB; Hoffman MD; Simon M; Petukhov PA; Tharp MD; Glant TT
Clin Exp Dermatol; 2011 Dec; 36(8):889-95. PubMed ID: 21790734
[TBL] [Abstract][Full Text] [Related]
16. Analysis of NLRP3, MVK and TNFRSF1A variants in adult Greek patients with autoinflammatory symptoms.
Karagianni P; Nezos A; Ioakeim F; Tzioufas AG; Moutsopoulos HM
Clin Exp Rheumatol; 2018; 36(6 Suppl 115):86-89. PubMed ID: 30418111
[TBL] [Abstract][Full Text] [Related]
17. Hereditary autoinflammatory syndromes: a Brazilian multicenter study.
Jesus AA; Fujihira E; Watase M; Terreri MT; Hilario MO; Carneiro-Sampaio M; Len CA; Oliveira SK; Rodrigues MC; Pereira RM; Bica B; Silva NA; Cavalcanti A; Marini R; Sztajnbok F; Quintero MV; Ferriani VP; Moraes-Vasconcelos D; Silva CA; Oliveira JB
J Clin Immunol; 2012 Oct; 32(5):922-32. PubMed ID: 22566169
[TBL] [Abstract][Full Text] [Related]
18. Inflammation in mice ectopically expressing human Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne (PAPA) Syndrome-associated PSTPIP1 A230T mutant proteins.
Wang D; Höing S; Patterson HC; Ahmad UM; Rathinam VA; Rajewsky K; Fitzgerald KA; Golenbock DT
J Biol Chem; 2013 Feb; 288(7):4594-601. PubMed ID: 23293022
[TBL] [Abstract][Full Text] [Related]
19. The systemic autoinflammatory diseases: inborn errors of the innate immune system.
Brydges S; Kastner DL
Curr Top Microbiol Immunol; 2006; 305():127-60. PubMed ID: 16724804
[TBL] [Abstract][Full Text] [Related]
20. Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.
De Pieri C; Vuch J; De Martino E; Bianco AM; Ronfani L; Athanasakis E; Bortot B; Crovella S; Taddio A; Severini GM; Tommasini A
Pediatr Rheumatol Online J; 2015; 13():11. PubMed ID: 25866490
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]