-
2
-
-
0032574208
-
Familial Mediterranean fever
-
BEN-CHETRIT E, LEVY M: Familial Mediterranean fever. Lancet 1998; 351: 659-64.
-
(1998)
Lancet
, vol.351
, pp. 659-664
-
-
BEN-CHETRIT, E.1
LEVY, M.2
-
3
-
-
16944365196
-
A candidate gene for familial Mediterranean fever
-
THE FRENCH FMF CONSORTIUM
-
THE FRENCH FMF CONSORTIUM: A candidate gene for familial Mediterranean fever. Nat Genet 1997; 17: 25-31.
-
(1997)
Nat Genet
, vol.17
, pp. 25-31
-
-
-
4
-
-
0030745449
-
Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever
-
THE INTERNATIONAL FMF CONSORTIUM
-
THE INTERNATIONAL FMF CONSORTIUM: Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 1997; 90: 797-807.
-
(1997)
Cell
, vol.90
, pp. 797-807
-
-
-
5
-
-
0033515520
-
Germline mutations in the extracellular domains of the 55kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammmatory syndromes
-
MCDERMOTT MF, AKSENTIJEVICH I, GALON J et al.: Germline mutations in the extracellular domains of the 55kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammmatory syndromes. Cell 1999; 97: 133-44.
-
(1999)
Cell
, vol.97
, pp. 133-144
-
-
MCDERMOTT, M.F.1
AKSENTIJEVICH, I.2
GALON, J.3
-
6
-
-
0034095570
-
TNFRSF1A mutations and autoinflammatory syndromes
-
GALON J, AKSENTIJEVICH I, MCDERMOTT MF, O'SHEA JJ, KASTNER DL: TNFRSF1A mutations and autoinflammatory syndromes. Curr Op Immunol 2000; 12: 479-86.
-
(2000)
Curr Op Immunol
, vol.12
, pp. 479-486
-
-
GALON, J.1
AKSENTIJEVICH, I.2
MCDERMOTT, M.F.3
O'SHEA, J.J.4
KASTNER, D.L.5
-
8
-
-
0034757551
-
BehcIcedil;et's disease: Infectious aetiology, new autoantigens, and HLA-B51
-
DIRESKENELI H: BehcIcedil;et's disease: infectious aetiology, new autoantigens, and HLA-B51. Ann Rheum Dis 2001; 60: 996-1002.
-
(2001)
Ann Rheum Dis
, vol.60
, pp. 996-1002
-
-
DIRESKENELI, H.1
-
9
-
-
0033625291
-
Behcet's disease in familial Mediterranean fever: Characterization of the association between the two diseases
-
SCHWARTZ T, LANGEVITZ P, ZEMER D, GAZIT E, PRAS M, LIVNEH A: Behcet's disease in familial Mediterranean fever: Characterization of the association between the two diseases. Semin Arthritis Rheum 2000; 29: 286-95.
-
(2000)
Semin Arthritis Rheum
, vol.29
, pp. 286-295
-
-
SCHWARTZ, T.1
LANGEVITZ, P.2
ZEMER, D.3
GAZIT, E.4
PRAS, M.5
LIVNEH, A.6
-
10
-
-
0025360899
-
Criteria for diagnosis of Behçet's disease
-
INTERNATIONAL STUDY GROUP OF BEHÇET'S DISEASE
-
INTERNATIONAL STUDY GROUP OF BEHÇET'S DISEASE: Criteria for diagnosis of Behçet's disease. Lancet 1990; 335: 1075-80.
-
(1990)
Lancet
, vol.335
, pp. 1075-1080
-
-
-
11
-
-
0031787901
-
Coexistence of familial Mediterranean fever with sacroiliitis and Behcet's disease: A rare occurrence
-
BIRLIK M, TUNCA M, HIZLI N, SOYTURK M, YENICERIOGLU Y, OZCAN MA: Coexistence of familial Mediterranean fever with sacroiliitis and Behcet's disease: A rare occurrence. Clin Rheumatol 1998; 17: 397-9.
-
(1998)
Clin Rheumatol
, vol.17
, pp. 397-399
-
-
BIRLIK, M.1
TUNCA, M.2
HIZLI, N.3
SOYTURK, M.4
YENICERIOGLU, Y.5
OZCAN, M.A.6
-
12
-
-
0036195579
-
Familial Mediterranean fever and Behcet's disease - are they associated?
-
BEN-CHETRIT E, COHEN R, CHAJEK-SHAUL T: Familial Mediterranean fever and Behcet's disease - are they associated? J Rheumatol 2002; 29: 530-4.
-
(2002)
J Rheumatol
, vol.29
, pp. 530-534
-
-
BEN-CHETRIT, E.1
COHEN, R.2
CHAJEK-SHAUL, T.3
-
13
-
-
0034268002
-
MEFV mutation in Behçet's disease
-
TOUITOU I, MAGNE X, MOLINARI N et al.: MEFV mutation in Behçet's disease. Human Mut 2000; 16: 271-2.
-
(2000)
Human Mut
, vol.16
, pp. 271-272
-
-
TOUITOU, I.1
MAGNE, X.2
MOLINARI, N.3
-
14
-
-
0029662248
-
Cytokines in Behçet's diseases
-
SAYINALP N, OEZCEBE OI, OEZDEMIR O, HAZNEDAROGLU CH, DUNDAR S, KIRAZLI S: Cytokines in Behçet's diseases. J Rheumatol 1996; 23: 321.
-
(1996)
J Rheumatol
, vol.23
, pp. 321
-
-
SAYINALP, N.1
OEZCEBE, O.I.2
OEZDEMIR, O.3
HAZNEDAROGLU, C.H.4
DUNDAR, S.5
KIRAZLI, S.6
-
15
-
-
13444310437
-
Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's disease
-
AMOURA Z, DODÉ C, HUE S et al.: Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's disease. Arthritis Rheum 2005; 52; 608-11.
-
(2005)
Arthritis Rheum
, vol.52
, pp. 608-611
-
-
AMOURA, Z.1
DODÉ, C.2
HUE, S.3
-
16
-
-
2342558725
-
The West side story: MEFV haplotype in Spanish FMF patients and controls, and evidence of high LD and a recombination 'hotspot' at the MEFV locus
-
ALDEA A, CALAFELL F, AROSTEGUI JI et al.: The West side story: MEFV haplotype in Spanish FMF patients and controls, and evidence of high LD and a recombination 'hotspot' at the MEFV locus. Hum Mutation 2004; 23: 399.
-
(2004)
Hum Mutation
, vol.23
, pp. 399
-
-
ALDEA, A.1
CALAFELL, F.2
AROSTEGUI, J.I.3
-
17
-
-
0141669189
-
MEFV mutations are increased in Behçet's disease (BD) and are associated with vascular involvement
-
ATAGUNDUZ P, ERGUN T, DIRESKENELI H: MEFV mutations are increased in Behçet's disease (BD) and are associated with vascular involvement. Clin Exp Rheumatol 2003; 21(suppl 30): S35-S37.
-
(2003)
Clin Exp Rheumatol
, vol.21
, Issue.SUPPL. 30
-
-
ATAGUNDUZ, P.1
ERGUN, T.2
DIRESKENELI, H.3
-
18
-
-
0035076326
-
A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMFBD)
-
LIVNEH A, AKSENTIJEVICH I, LANGEVITZ P et al.: A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMFBD). Eur J Hum Genet 2001; 9: 191-6.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 191-196
-
-
LIVNEH, A.1
AKSENTIJEVICH, I.2
LANGEVITZ, P.3
-
19
-
-
0029079903
-
Familial Mediterranean fever in the "chuetas" of Mallorca: Origin in inquisition?
-
BUADES J, BEN-CHETRIT E, LEVY M: Familial Mediterranean fever in the "chuetas" of Mallorca: Origin in inquisition? Isr J Med Sci 1995; 31: 497-9.
-
(1995)
Isr J Med Sci
, vol.31
, pp. 497-499
-
-
BUADES, J.1
BEN-CHETRIT, E.2
LEVY, M.3
|