-
1
-
-
0021802275
-
Familial granulomatous synovitis, uveitis, and cranial neuropathies
-
DOI 10.1016/0002-9343(85)90286-4
-
Jabs DA, Houk JL, Bias WB, Arnett FC, et al. Familial granulomatous synovitis, uveitis, and cranial neuropathies. Am J Med 1985;78:801-4. (Pubitemid 15008235)
-
(1985)
American Journal of Medicine
, vol.78
, Issue.5
, pp. 801-804
-
-
Jabs, D.A.1
Houk, J.L.2
Bias, W.B.3
Arnett, F.C.4
-
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
-
DOI 10.1002/art.10618
-
Wang X, Kuivaniemi H, Bonavita G, Mutkus L, et al. CARD15 mutations in familial granulomatosis syndromes: A study of the original Blau syndrome kindred and other familieswith large-vessel arteritis and cranial neuropathy. Arthritis Rheum 2002;46:3041-5. (Pubitemid 35315899)
-
(2002)
Arthritis and Rheumatism
, vol.46
, Issue.11
, pp. 3041-3045
-
-
Wang, X.1
Kuivaniemi, H.2
Bonavita, G.3
Mutkus, L.4
Mau, U.5
Blau, E.6
Inohara, N.7
Nunez, G.8
Tromp, G.9
Williams, C.J.10
-
3
-
-
0141747229
-
Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation
-
DOI 10.1016/S0161-6420(03)00717-6
-
Kurokawa T, Kikuchi T, Ohta K, Imai H, Yoshimura N. Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation. Ophthalmology 2003;110:2040-44. (Pubitemid 37163327)
-
(2003)
Ophthalmology
, vol.110
, Issue.10
, pp. 2040-2044
-
-
Kurokawa, T.1
Kikuchi, T.2
Ohta, K.3
Imai, H.4
Yoshimura, N.5
-
4
-
-
0141570485
-
With a mere nod, uveitis enters a new era
-
DOI 10.1016/S0002-9394(03)00569-5
-
Rosenbaum JT, Planck SR, Davey MP, Iwanaga Y, Kurz DE, Martin TM. With a mere nod, uveitis enters a new era. Am J Ophthalmol 2003;136:729-32. (Pubitemid 37153190)
-
(2003)
American Journal of Ophthalmology
, vol.136
, Issue.4
, pp. 729-732
-
-
Rosenbaum, J.T.1
Planck, S.R.2
Davey, M.P.3
Iwanaga, Y.4
Kurz, D.E.5
Martin, T.M.6
-
5
-
-
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
-
DOI 10.1002/art.22966
-
Arostegui J, 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 and Rheumatism 2007;56:3805-13. (Pubitemid 350100713)
-
(2007)
Arthritis and Rheumatism
, vol.56
, Issue.11
, pp. 3805-3813
-
-
Arostegui, J.I.1
Arnal, C.2
Merino, R.3
Modesto, C.4
Carballo, M.A.5
Moreno, P.6
Garcia-Consuegra, J.7
Naranjo, A.8
Ramos, E.9
De Paz, P.10
Rius, J.11
Plaza, S.12
Yague, J.13
-
6
-
-
0037452968
-
Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases
-
DOI 10.1073/pnas.0530276100
-
Chamaillard M, Philpott D, Girardin SE, et al. Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases. Proc Natl Acad Sci U S A 2003;100:3455-60. (Pubitemid 36356605)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.6
, pp. 3455-3460
-
-
Chamaillard, M.1
Philpott, D.2
Girardin, S.E.3
Zouali, H.4
Lesage, S.5
Chareyre, F.6
Bui, T.H.7
Giovannini, M.8
Zaehringer, U.9
Penard-Lacronique, V.10
Sansonetti, P.J.11
Hugot, J.-P.12
Thomas, G.13
-
7
-
-
58249095950
-
Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis
-
Okafujim I, Nishikomori R, Kanazawa N, et al. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis. Arth Rheum 2009;60:242-50.
-
(2009)
Arth Rheum
, vol.60
, pp. 242-250
-
-
Okafujim, I.1
Nishikomori, R.2
Kanazawa, N.3
-
8
-
-
0028035092
-
Preschool sarcoidosis manifesting as juvenile rheumatoid arthritis: A case report and a review of the literature of Japanese cases
-
Ukae S, Tsutsumi H, Adachi N, Takahashi H, Kato F, Chiba S. Pre-school sarcoidosis manifesting as juvenile rheumatoid arthritis: A case report and a review of the literature of Japanese cases. Acta Paediatrica Japonica (Overseas Edition) 1994;36:515-8. (Pubitemid 24319574)
-
(1994)
Acta Paediatrica Japonica (Overseas Edition)
, vol.36
, Issue.5
, pp. 515-518
-
-
Ukae, S.1
Tsutsumi, H.2
Adachi, N.3
Takahashi, H.4
Kato, F.5
Chiba, S.6
-
9
-
-
19944431022
-
Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-B activation: Common genetic etiology with Blau syndrome
-
DOI 10.1182/blood-2004-07-2972
-
Kanazawa N, Okafuji I, Kambe N, et al. Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-B activation: Common genetic etiology with Blau syndrome. Blood 2005;105:1195-7. (Pubitemid 40170893)
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 1195-1197
-
-
Kanazawa, N.1
Okafuji, I.2
Kambe, N.3
Nishikomori, R.4
Nakata-Hizume, M.5
Nagai, S.6
Fuji, A.7
Yuasa, T.8
Manki, A.9
Sakurai, Y.10
Nakajima, M.11
Kobayashi, H.12
Fujiwara, I.13
Tsutsumi, H.14
Utani, A.15
Nishigori, C.16
Heike, T.17
Nakahata, T.18
Miyachi, Y.19
|