-
1
-
-
0142257968
-
Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15)
-
Martin TM, Doyle TM, Smith Jr. Dinulesu D, et al. Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15). Am J Ophthalmol 2003;136: 933-935.
-
(2003)
Am J Ophthalmol
, vol.136
, pp. 933-935
-
-
Martin, T.M.1
Doyle, T.M.2
Smith Jr., D.D.3
-
3
-
-
77954754916
-
A genome-wide linkage analysis in 181 German sarcoidosis families using clustered biallelic markers
-
Fischer A, Nothagel M, Schürmann M, et al. A genome-wide linkage analysis in 181 German sarcoidosis families using clustered biallelic markers. Chest 2010; 138(1):151-157.
-
(2010)
Chest
, vol.138
, Issue.1
, pp. 151-157
-
-
Fischer A, N.1
-
4
-
-
0022213722
-
Familial granulomatous arthritis, iritis and rash
-
Blau EB. Familial granulomatous arthritis, iritis and rash. J Pediat. 1985;107:689-693.
-
(1985)
J Pediat.
, vol.107
, pp. 689-693
-
-
Blau, E.B.1
-
5
-
-
0021802275
-
Familial granu-lomatous synovitis, uveitis, and cranial neuropathies
-
Jabs DA, Houk JL, Bias WB, Arnett FC. Familial granu-lomatous synovitis, uveitis, and cranial neuropathies. Am J Med 1985;78:801-804.
-
(1985)
Am J Med
, vol.78
, pp. 801-804
-
-
Jabs, D.A.1
Houk, J.L.2
Bias, W.B.3
Arnett, F.C.4
-
6
-
-
0022542441
-
Early-onset sarcoidosis and "familial granu-lomatous arthritis (arteritis)": The same disease
-
Miller III JJ. Early-onset sarcoidosis and "familial granu-lomatous arthritis (arteritis)": The same disease. J Pediatr 1986;109(2):109387- 109388.
-
(1986)
J Pediatr
, vol.109
, Issue.2
, pp. 109387-109388
-
-
Miller III, J.J.1
-
7
-
-
0029981988
-
Liver involvement in familial granulomatous arthritis (Blau syndrome)
-
Saini SK and Rose CD. Liver involvement in familial granulomatous arthritis (Blau syndrome). J Rheum 1996;23: 396-399.
-
(1996)
J Rheum
, vol.23
, pp. 396-399
-
-
Saini, S.K.1
Rose, C.D.2
-
8
-
-
0031682554
-
Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions
-
Ting SS, Ziegler J, Fischer E. Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions. J Pediatr 1998;133:450-452.
-
(1998)
J Pediatr
, vol.133
, pp. 450-452
-
-
Ting, S.S.1
Ziegler, J.2
Fischer, E.3
-
9
-
-
36849095673
-
Central nervous system involvement in Blau syndrome: A new feature of the syndrome?
-
Emaminia A, Nabavi M, Mousavi NM, Kashef S. Central nervous system involvement in Blau syndrome: A new feature of the syndrome? J Rheumatol 2007;34(12): 2504-2505.
-
(2007)
J Rheumatol
, vol.34
, Issue.12
, pp. 2504-2505
-
-
Emaminia, A.1
Nabavi, M.2
Mousavi, N.M.3
Kashef, S.4
-
10
-
-
14144252856
-
Blau syndrome presenting with ichthyosis
-
Masel G, Halbert A. Blau syndrome presenting with ichthyosis. Australas J Dermatol 2005;46:29-32.
-
(2005)
Australas J Dermatol
, vol.46
, pp. 29-32
-
-
Masel, G.1
Halbert, A.2
-
11
-
-
0036846291
-
CARD15 mutations in familial granulomatosis syndromes
-
Wang X, Kuivaniemi H, Bonavita G, et al. CARD15 mutations in familial granulomatosis syndromes. Arthritis Rheum 2002;46(11):3041-3045.
-
(2002)
Arthritis Rheum
, vol.46
, Issue.11
, pp. 3041-3045
-
-
Wang, X.1
Kuivaniemi, H.2
Bonavita, G.3
-
12
-
-
77952250064
-
Sinus of vaslava aneurysm in Blau's syndrome
-
Mourad F, Tang A. Sinus of vaslava aneurysm in Blau's syndrome. J Cardiothorac Surd 2010;5:16.
-
(2010)
J Cardiothorac Surd
, vol.5
, pp. 16
-
-
Mourad, F.1
Tang, A.2
-
13
-
-
84865758181
-
Blau arteritis resembling Takayasu Disease with a novel NOD2 Mutation
-
Raju P, Hasija R, Touitou I, et al. Blau arteritis resembling Takayasu Disease with a novel NOD2 Mutation. J Rheumatol 2012;39:1888-1892.
-
(2012)
J Rheumatol
, vol.39
, pp. 1888-1892
-
-
Raju, P.1
Hasija, R.2
Touitou, I.3
-
14
-
-
66449110515
-
NOD2-Associated pediatric granulomatous arthritis, an expanding pheno-type: Study of an international registry and a national cohort in Spain
-
Rose CD, Arostegui JI, Martin TM, et al. NOD2-Associated pediatric granulomatous arthritis, an expanding pheno-type: Study of an international registry and a national cohort in Spain. Arthritis Rheum 2009;60:1797-1803.
-
(2009)
Arthritis Rheum
, vol.60
, pp. 1797-1803
-
-
Rose, C.D.1
Arostegui, J.I.2
Martin, T.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
-
17
-
-
19244364857
-
Genetic linkage of familial granulomatosis inflammatory arthritis, skin rash and uveitis to chromosome 16
-
Tromp G, Kuivaniemi H, Raphael S, et al. Genetic linkage of familial granulomatosis inflammatory arthritis, skin rash and uveitis to chromosome 16. Am J Hum Genet 1996; 59:1097-1107.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1097-1107
-
-
Tromp, G.1
Kuivaniemi, H.2
Raphael, S.3
-
18
-
-
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
-
20
-
-
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 Derm 2004;122:851-852.
-
(2004)
J Invest Derm
, vol.122
, pp. 851-852
-
-
Kanazawa, N.1
Matsushima, S.2
Kambe, N.3
-
21
-
-
13444281923
-
Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis
-
Rose 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
-
-
Rose, C.D.1
Doyle, T.M.2
McIlvain-Simpson, G.3
-
23
-
-
79956218796
-
Uveitis in Blau syndrome from a de novo mutation of the NOD2/CARD15 gene
-
Raiji VR, Miller MM, Jung LK. Uveitis in Blau syndrome from a de novo mutation of the NOD2/CARD15 gene. J AAPOS 2011;15:205-207.
-
(2011)
J AAPOS
, vol.15
, pp. 205-207
-
-
Raiji, V.R.1
Miller, M.M.2
Jung, L.K.3
-
24
-
-
66449102948
-
Incomplete penetrance of the NOD2 E383K substitution among members of a pediatric granulomatous arthritis pedigree
-
Saulsbury FT, Wouters CH, Martin TM, et al. Incomplete penetrance of the NOD2 E383K substitution among members of a pediatric granulomatous arthritis pedigree. Arthritis Rheum 2009;60:1804-1806.
-
(2009)
Arthritis Rheum
, vol.60
, pp. 1804-1806
-
-
Saulsbury, F.T.1
Wouters, C.H.2
Martin, T.M.3
-
25
-
-
19944431022
-
Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-KB 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-KB activation: Common genetic etiology with Blau syndrome. Blood 2005;10(3):1195-1197.
-
(2005)
Blood
, vol.10
, Issue.3
, pp. 1195-1197
-
-
Kanazawa, N.1
Okafuji, I.2
Kambe, N.3
-
26
-
-
33845189002
-
Blau syndrome associated with a CARD15/NOD2 mutation
-
Snyers B, Dahan K. Blau syndrome associated with a CARD15/NOD2 mutation. Am J Ophthalmol 2006;142(6): 1421089-1421092.
-
(2006)
Am J Ophthalmol
, vol.142
, Issue.6
, pp. 1421089-1421092
-
-
Snyers, B.1
Dahan, K.2
-
27
-
-
0035895992
-
Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-KB
-
Ogura Y, Inohara N, Benito A, et al. Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-KB. J Biol Chem 2001;276(7):4812-4818.
-
(2001)
J Biol Chem
, vol.276
, Issue.7
, pp. 4812-4818
-
-
Ogura, Y.1
Inohara, N.2
Benito, A.3
-
28
-
-
20444459502
-
NOD2 and Crohn's disease: Loss or gain of function?
-
Eckmann L, Karin M. NOD2 and Crohn's disease: Loss or gain of function? Immunity 2005;22(6):661-667
-
(2005)
Immunity
, vol.22
, Issue.6
, pp. 661-667
-
-
Eckmann, L.1
Karin, M.2
-
29
-
-
84866874147
-
Blau syndrome, clinical and genetic aspects
-
Sfriso P, Caso F, Tognon S, et al. Blau syndrome, clinical and genetic aspects. Autoimmunity Reviews 2012;12:44-51.
-
(2012)
Autoimmunity Reviews
, vol.12
, pp. 44-51
-
-
Sfriso, P.1
Caso, F.2
Tognon, S.3
-
30
-
-
45549085856
-
NOD2, the gene responsible for familial granulomatous uveitis, in a mouse model of uveitis
-
Rosenzweig HL, Martin TM, Jann MM, et al. NOD2, the gene responsible for familial granulomatous uveitis, in a mouse model of uveitis. Invest Ophthalmol Vis Sci 2008;49: 1518-1524.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 1518-1524
-
-
Rosenzweig, H.L.1
Martin, T.M.2
Jann, M.M.3
-
31
-
-
64049102506
-
Nucleotide oligomerization domain-2(NOD2) induced uveitis: Dependence on IFN gamma
-
Apr
-
Rosenzweig HL, Kawaguchi T, Martin TM, et al. Nucleotide oligomerization domain-2(NOD2) induced uveitis: Dependence on IFN gamma. IOVS 2009 Apr: 1739-1745.
-
(2009)
IOVS
, pp. 1739-1745
-
-
Rosenzweig, H.L.1
Kawaguchi, T.2
Martin, T.M.3
-
32
-
-
0141570485
-
With a mere nod, uveitis enters a new era
-
Rosenbaum JT, Planck SR, Davey MP, et al. With a mere nod, uveitis enters a new era. Am J Ophthalmol 2003;136: 729-732.
-
(2003)
Am J Ophthalmol
, vol.136
, pp. 729-732
-
-
Rosenbaum, J.T.1
Planck, S.R.2
Davey, M.P.3
-
33
-
-
33646051863
-
Human endo-thelial cells express NOD2/CARD15 and increase IL-6 secretion in response to muramyl dipeptide
-
Davey MP, Martin TM, Planck SR, et al. Human endo-thelial cells express NOD2/CARD15 and increase IL-6 secretion in response to muramyl dipeptide. Microvascular Res 2006;71:103-107.
-
(2006)
Microvascular Res
, vol.71
, pp. 103-107
-
-
Davey, M.P.1
Martin, T.M.2
Planck, S.R.3
-
34
-
-
48649100466
-
Activation of NOD2 in vivo induces IL-1beta production in the eye via caspase-1 but results in ocular inflammation independently of IL-1 signaling
-
Aug
-
Rosenzweig HL, Martin TM, Planck SR, et al. Activation of NOD2 in vivo induces IL-1beta production in the eye via caspase-1 but results in ocular inflammation independently of IL-1 signaling. J Leukoc Biol 2008 Aug;84(2): 529-536.
-
(2008)
J Leukoc Biol
, vol.84
, Issue.2
, pp. 529-536
-
-
Rosenzweig, H.L.1
Martin, T.M.2
Planck, S.R.3
-
35
-
-
73849121209
-
Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry
-
Travassos LH, Carneiro LA, Ramjeet M, et al. Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry. Nat Immunol 2010;11:55-62.
-
(2010)
Nat Immunol
, vol.11
, pp. 55-62
-
-
Travassos, L.H.1
Carneiro, L.A.2
Ramjeet, M.3
-
36
-
-
73849151394
-
NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation
-
Cooney R, Baker J, Brain O, et al. NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation. Nat Med 2010;16:90-97.
-
(2010)
Nat Med
, vol.16
, pp. 90-97
-
-
Cooney, R.1
Baker, J.2
Brain, O.3
-
37
-
-
84863989711
-
Meta-analysis of NOD2/CARD15 polymorphisms with psoriasis and psoriatic arthritis
-
Zhu K, Yin X, Tang X, et al. Meta-analysis of NOD2/CARD15 polymorphisms with psoriasis and psoriatic arthritis. Rheumatol Int 2012;32(7):1893-1900.
-
(2012)
Rheumatol Int
, vol.32
, Issue.7
, pp. 1893-1900
-
-
Zhu, K.1
Yin, X.2
Tang, X.3
-
38
-
-
77951721712
-
Insufficient evidence for the association of NOD2/CARD15 or other inflammatory bowel disease associated markers on GVHD incidence or other adverse outcomes in T-replete unrelated donor transplantation
-
Nguyen Y, Al-Lehibi A, Gorbe E, et al. Insufficient evidence for the association of NOD2/CARD15 or other inflammatory bowel disease associated markers on GVHD incidence or other adverse outcomes in T-replete, unrelated donor transplantation. Blood 2010;115(17):3625-3631.
-
(2010)
Blood
, vol.115
, Issue.17
, pp. 3625-3631
-
-
Nguyen, Y.1
Al-Lehibi, A.2
Gorbe, E.3
-
39
-
-
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
-
40
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Chrohn's disease
-
Ogura Y, Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Chrohn's disease. Nature 2001;411:603-606.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
-
41
-
-
17644366913
-
NOD-LRR proteins: Role in host-microbial interactions and inflammatory disease
-
Inohara H, Chamaillard M, McDonald C, Nuñez G. NOD-LRR proteins: Role in host-microbial interactions and inflammatory disease. Annu Rev Biochem 2005;74: 355-383.
-
(2005)
Annu Rev Biochem
, vol.74
, pp. 355-383
-
-
Inohara, H.1
Chamaillard, M.2
McDonald, C.3
Nuñez, G.4
-
42
-
-
33845707639
-
Favourable effect of TNF-alpha inhibitor (infliximab) on Blau syndrome in monozygotic twins with a de novo CARD15 mutation
-
Milman N, Andersen CB, Hansen A, et al. Favourable effect of TNF-alpha inhibitor (infliximab) on Blau syndrome in monozygotic twins with a de novo CARD15 mutation. APMIS 2006;14:912-919.
-
(2006)
APMIS
, vol.14
, pp. 912-919
-
-
Milman, N.1
Andersen, C.B.2
Hansen, A.3
-
44
-
-
74849116666
-
Thalidomide dramatically improves the symptoms of early-onset sarcoidosis/Blau syndrome: Its possible action and mechanism
-
Yasui K, Yashiro M, Tsuge M, et al. Thalidomide dramatically improves the symptoms of early-onset sarcoidosis/Blau syndrome: Its possible action and mechanism. Arthritis Rheum 2010;63:250-257.
-
(2010)
Arthritis Rheum
, vol.63
, pp. 250-257
-
-
Yasui, K.1
Yashiro, M.2
Tsuge, M.3
-
46
-
-
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
-
Nov
-
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 Nov;56(11): 3805-3813.
-
(2007)
Arthritis Rheum
, vol.56
, Issue.11
, pp. 3805-3813
-
-
Aróstegui, J.I.1
Arnal, C.2
Merino, R.3
-
47
-
-
59649127380
-
The NOD2 defect in Blau Syndrome does not result in excess interleukin-1 activity
-
Martin TM, Zhang Z, Kurz P, et al. The NOD2 defect in Blau Syndrome does not result in excess interleukin-1 activity. Arthritis Rheum 2009;60(2):611-618.
-
(2009)
Arthritis Rheum
, vol.60
, Issue.2
, pp. 611-618
-
-
Martin, T.M.1
Zhang, Z.2
Kurz, P.3
-
48
-
-
84873814538
-
Clinical and transcrip-tional response to the long-acting interleukin-1 blocker canakinumab in Blau syndrome-related uveitis
-
Simonini G, Xu Z, Caputo R, et al. Clinical and transcrip-tional response to the long-acting interleukin-1 blocker canakinumab in Blau syndrome-related uveitis. Arthritis Rheum 2013;65(2):513-518.
-
(2013)
Arthritis Rheum
, vol.65
, Issue.2
, pp. 513-518
-
-
Simonini, G.1
Xu, Z.2
Caputo, R.3
|