163 related articles for article (PubMed ID: 14516815)
1. With a mere nod, uveitis enters a new era.
Rosenbaum JT; Planck SR; Davey MP; Iwanaga Y; Kurz DE; Martin TM
Am J Ophthalmol; 2003 Oct; 136(4):729-32. PubMed ID: 14516815
[TBL] [Abstract][Full Text] [Related]
2. Nucleotide-binding oligomerization domain containing 2: structure, function, and diseases.
Yao Q
Semin Arthritis Rheum; 2013 Aug; 43(1):125-30. PubMed ID: 23352252
[TBL] [Abstract][Full Text] [Related]
3. Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15).
Martin TM; Doyle TM; Smith JR; Dinulescu D; Rust K; Rosenbaum JT
Am J Ophthalmol; 2003 Nov; 136(5):933-5. PubMed ID: 14597055
[TBL] [Abstract][Full Text] [Related]
4. A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members.
Milman N; Ursin K; Rødevand E; Nielsen FC; Hansen TV
Scand J Rheumatol; 2009; 38(3):190-7. PubMed ID: 19169908
[TBL] [Abstract][Full Text] [Related]
5. NOD2, the gene responsible for familial granulomatous uveitis, in a mouse model of uveitis.
Rosenzweig HL; Martin TM; Jann MM; Planck SR; Davey MP; Kobayashi K; Flavell RA; Rosenbaum JT
Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1518-24. PubMed ID: 18385071
[TBL] [Abstract][Full Text] [Related]
6. A Novel Pathogenic
Rodrigues FG; Petrushkin H; Webster AR; Bickerstaff M; Moraitis E; Rowczenio D; Aróstegui JI; Westcott M
Ophthalmic Genet; 2021 Dec; 42(6):753-764. PubMed ID: 34251956
[TBL] [Abstract][Full Text] [Related]
7. Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis.
Takada S; Saito MK; Kambe N
G Ital Dermatol Venereol; 2020 Oct; 155(5):537-541. PubMed ID: 32618442
[TBL] [Abstract][Full Text] [Related]
8. Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation.
Kurokawa T; Kikuchi T; Ohta K; Imai H; Yoshimura N
Ophthalmology; 2003 Oct; 110(10):2040-4. PubMed ID: 14522785
[TBL] [Abstract][Full Text] [Related]
9. Sporadic Blau syndrome with onset of widespread granulomatous dermatitis in the newborn period.
Stoevesandt J; Morbach H; Martin TM; Zierhut M; Girschick H; Hamm H
Pediatr Dermatol; 2010; 27(1):69-73. PubMed ID: 20199415
[TBL] [Abstract][Full Text] [Related]
10. CARD15 mutations in Blau syndrome.
Miceli-Richard C; Lesage S; Rybojad M; Prieur AM; Manouvrier-Hanu S; Häfner R; Chamaillard M; Zouali H; Thomas G; Hugot JP
Nat Genet; 2001 Sep; 29(1):19-20. PubMed ID: 11528384
[TBL] [Abstract][Full Text] [Related]
11. Blau syndrome revisited.
Rose CD; Martin TM; Wouters CH
Curr Opin Rheumatol; 2011 Sep; 23(5):411-8. PubMed ID: 21788900
[TBL] [Abstract][Full Text] [Related]
12. Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism.
Mensa-Vilaro A; Cham WT; Tang SP; Lim SC; González-Roca E; Ruiz-Ortiz E; Ariffin R; Yagüe J; Aróstegui JI
Arthritis Rheumatol; 2016 Apr; 68(4):1039-44. PubMed ID: 26606664
[TBL] [Abstract][Full Text] [Related]
13. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.
Okafuji I; Nishikomori R; Kanazawa N; Kambe N; Fujisawa A; Yamazaki S; Saito M; Yoshioka T; Kawai T; Sakai H; Tanizaki H; Heike T; Miyachi Y; Nakahata T
Arthritis Rheum; 2009 Jan; 60(1):242-50. PubMed ID: 19116920
[TBL] [Abstract][Full Text] [Related]
14. Blau syndrome with a rare mutation in exon 9 of
Velickovic J; Silan F; Bir FD; Silan C; Albuz B; Ozdemir O
Autoimmunity; 2019; 52(7-8):256-263. PubMed ID: 31556326
[TBL] [Abstract][Full Text] [Related]
15. NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.
Aróstegui JI; Arnal C; Merino R; Modesto C; Antonia Carballo M; Moreno P; García-Consuegra J; Naranjo A; Ramos E; de Paz P; Rius J; Plaza S; Yagüe J
Arthritis Rheum; 2007 Nov; 56(11):3805-13. PubMed ID: 17968944
[TBL] [Abstract][Full Text] [Related]
16. Blau syndrome associated with a CARD15/NOD2 mutation.
Snyers B; Dahan K
Am J Ophthalmol; 2006 Dec; 142(6):1089-92. PubMed ID: 17157607
[TBL] [Abstract][Full Text] [Related]
17. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.
Rosé CD; Doyle TM; McIlvain-Simpson G; Coffman JE; Rosenbaum JT; Davey MP; Martin TM
J Rheumatol; 2005 Feb; 32(2):373-5. PubMed ID: 15693102
[TBL] [Abstract][Full Text] [Related]
18. Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis.
Zhong Z; Ding J; Su G; Liao W; Gao Y; Zhu Y; Deng Y; Li F; Du L; Gao Y; Yang P
Ophthalmology; 2022 Jul; 129(7):821-828. PubMed ID: 35314268
[TBL] [Abstract][Full Text] [Related]
19. Blau syndrome, the prototypic auto-inflammatory granulomatous disease.
Wouters CH; Maes A; Foley KP; Bertin J; Rose CD
Pediatr Rheumatol Online J; 2014; 12():33. PubMed ID: 25136265
[TBL] [Abstract][Full Text] [Related]
20. A new CARD15 mutation in Blau syndrome.
van Duist MM; Albrecht M; Podswiadek M; Giachino D; Lengauer T; Punzi L; De Marchi M
Eur J Hum Genet; 2005 Jun; 13(6):742-7. PubMed ID: 15812565
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]