-
1
-
-
0022213722
-
Familial granulomatous arthritis, iritis, and rash
-
Blau EB. Familial granulomatous arthritis, iritis, and rash. J Pediatr 1985 107 : 689 693.
-
(1985)
J Pediatr
, vol.107
, pp. 689-693
-
-
Blau, E.B.1
-
2
-
-
0036846291
-
CARD15 mutations in familial granulomatosis syndromes: A study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy
-
Wang X, Kuivaniemi H, Bonavita G et al. CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy. Arthritis Rheum 2002 46 : 3041 3045.
-
(2002)
Arthritis Rheum
, vol.46
, pp. 3041-3045
-
-
Wang, X.1
Kuivaniemi, H.2
Bonavita, G.3
-
3
-
-
33750345391
-
Pediatric granulomatous arthritis: An international registry
-
Rosé CD, Wouters CH, Meiorin S et al. Pediatric granulomatous arthritis: an international registry. Arthritis Rheum 2006 54 : 3337 3344.
-
(2006)
Arthritis Rheum
, vol.54
, pp. 3337-3344
-
-
Rosé, C.D.1
Wouters, C.H.2
Meiorin, S.3
-
4
-
-
36048981805
-
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 et al. 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. Arthritis Rheum 2007 56 : 3805 3813.
-
(2007)
Arthritis Rheum
, vol.56
, pp. 3805-3813
-
-
Aróstegui, J.I.1
Arnal, C.2
Merino, R.3
-
5
-
-
58249095950
-
Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis
-
Okafuji I, Nishikomori R, Kanazawa N et al. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis. Arthritis Rheum 2009 60 : 242 250.
-
(2009)
Arthritis Rheum
, vol.60
, pp. 242-250
-
-
Okafuji, I.1
Nishikomori, R.2
Kanazawa, N.3
-
7
-
-
1842740034
-
Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation
-
Kanazawa N, Matsushima S, Kambe N et al. Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation. J Invest Dermatol 2004 122 : 851 852.
-
(2004)
J Invest Dermatol
, vol.122
, pp. 851-852
-
-
Kanazawa, N.1
Matsushima, S.2
Kambe, N.3
-
8
-
-
19944431022
-
Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-κB activation: Common genetic etiology with Blau syndrome
-
Kanazawa N, Okafuji I, Kambe N et al. Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-κB activation: common genetic etiology with Blau syndrome. Blood 2005 105 : 1195 1197.
-
(2005)
Blood
, vol.105
, pp. 1195-1197
-
-
Kanazawa, N.1
Okafuji, I.2
Kambe, N.3
-
9
-
-
13444281923
-
Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis
-
Rosé CD, Doyle TM, McIlvain-Simpson G et al. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis. J Rheumatol 2005 32 : 373 375.
-
(2005)
J Rheumatol
, vol.32
, pp. 373-375
-
-
Rosé, C.D.1
Doyle, T.M.2
McIlvain-Simpson, G.3
-
11
-
-
0037452968
-
Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases
-
Chamaillard M, Philpott D, Girardin SE et al. Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases. Proc Natl Acad Sci USA 2003 100 : 3455 3460.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 3455-3460
-
-
Chamaillard, M.1
Philpott, D.2
Girardin, S.E.3
-
12
-
-
0012722659
-
NOD2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection
-
Girardin SE, Boneca IG, Viala J et al. NOD2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection. J Biol Chem 2003 278 : 8869 8872.
-
(2003)
J Biol Chem
, vol.278
, pp. 8869-8872
-
-
Girardin, S.E.1
Boneca, I.G.2
Viala, J.3
-
13
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001 411 : 599 603.
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
-
14
-
-
0036202885
-
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
-
Cuthbert AP, Fisher SA, Mirza MM et al. The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology 2002 122 : 867 874.
-
(2002)
Gastroenterology
, vol.122
, pp. 867-874
-
-
Cuthbert, A.P.1
Fisher, S.A.2
Mirza, M.M.3
-
15
-
-
0036895932
-
Multifocal choroiditis in patients with familial juvenile systemic granulomatosis
-
Latkany PA, Jabs DA, Smith JR et al. Multifocal choroiditis in patients with familial juvenile systemic granulomatosis. Am J Ophthalmol 2002 134 : 897 904.
-
(2002)
Am J Ophthalmol
, vol.134
, pp. 897-904
-
-
Latkany, P.A.1
Jabs, D.A.2
Smith, J.R.3
|