-
1
-
-
44449086297
-
Diagnosis and management of autoinflammatory diseases in childhood
-
(in press).
-
Gattorno M, Federici S, Pelagatti MA et al. Diagnosis and management of autoinflammatory diseases in childhood. J Clin Immunol Suppl 2008 (in press).
-
(2008)
J Clin Immunol Suppl
-
-
Gattorno, M.1
Federici, S.2
Pelagatti, M.A.3
-
2
-
-
33645458522
-
Familial Mediterranean fever and other autoinflammatory syndromes: Evaluation of the patient with recurrent fever
-
Samuels J, Ozen S. Familial Mediterranean fever and other autoinflammatory syndromes: evaluation of the patient with recurrent fever. Curr Opin Rheumatol 2006;18:108-17.
-
(2006)
Curr Opin Rheumatol
, vol.18
, pp. 108-17
-
-
Samuels, J.1
Ozen, S.2
-
3
-
-
34147145971
-
Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis
-
Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh A. Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol 2007;36:48-52.
-
(2007)
Scand J Rheumatol
, vol.36
, pp. 48-52
-
-
Rabinovich, E.1
Shinar, Y.2
Leiba, M.3
Ehrenfeld, M.4
Langevitz, P.5
Livneh, A.6
-
4
-
-
34249830128
-
Autoinflammatory gene mutations in Behçet's disease
-
Koné-Paut I, Sanchez E, Le Quellec A, Manna R, Touitou I. Autoinflammatory gene mutations in Behçet's disease. Ann Rheum Dis 2007;66:832-4.
-
(2007)
Ann Rheum Dis
, vol.66
, pp. 832-4
-
-
Koné-Paut, I.1
Sanchez, E.2
Le Quellec, A.3
Manna, R.4
Touitou, I.5
-
5
-
-
15944398723
-
MEFV gene is a probable susceptibility gene for Behçet's disease
-
Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC. MEFV gene is a probable susceptibility gene for Behçet's disease. Scand J Rheumatol 2005;34:56-8.
-
(2005)
Scand J Rheumatol
, vol.34
, pp. 56-8
-
-
Imirzalioglu, N.1
Dursun, A.2
Tastan, B.3
Soysal, Y.4
Yakicier, M.C.5
-
6
-
-
33645883525
-
Increased frequency of mutations in the gene responsible for familial Mediterranean fever (MEFV) in a cohort of patients with ulcerative colitis: Evidence for a potential disease-modifying effect?
-
Giaglis S, Mimidis K, Papadopoulos V, Thomopoulos K, Sidiropoulos P, Rafail S, Nikolopoulou V, Fragouli E, Kartalis G, Tzioufas A, Boumpas D, Ritis K. Increased frequency of mutations in the gene responsible for familial Mediterranean fever (MEFV) in a cohort of patients with ulcerative colitis: evidence for a potential disease-modifying effect? Dig Dis Sci 2006;51:687-92.
-
(2006)
Dig Dis Sci
, vol.51
, pp. 687-92
-
-
Giaglis, S.1
Mimidis, K.2
Papadopoulos, V.3
Thomopoulos, K.4
Sidiropoulos, P.5
Rafail, S.6
Nikolopoulou, V.7
Fragouli, E.8
Kartalis, G.9
Tzioufas, A.10
Boumpas, D.11
Ritis, K.12
-
7
-
-
84895913579
-
The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy
-
May 23 [Epub ahead of print].
-
Sari S, Egritas O, Dalgic B. The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy. Eur J Pediatr. 2007 May 23 [Epub ahead of print].
-
(2007)
Eur J Pediatr
-
-
Sari, S.1
Egritas, O.2
Dalgic, B.3
-
9
-
-
0019425358
-
Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation
-
Prieur AM, Griscelli C. Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation. J Pediatr 1981;99:79-83.
-
(1981)
J Pediatr
, vol.99
, pp. 79-83
-
-
Prieur, A.M.1
Griscelli, C.2
-
10
-
-
0021992710
-
Infantile multisystem inflammatory disease: A specific syndrome?
-
3
-
Yarom A, Rennebohm RM, Levinson JE. Infantile multisystem inflammatory disease: a specific syndrome? J Pediatr 1985;106(3):390-6.
-
(1985)
J Pediatr
, vol.106
, pp. 390-6
-
-
Yarom, A.1
Rennebohm, R.M.2
Levinson, J.E.3
-
11
-
-
33645800192
-
Chronic infantile neurological cutaneous and articular syndrome-an early description
-
Travers R, Allen R. Chronic infantile neurological cutaneous and articular syndrome-an early description. J Rheumatol 2006;33:822-4.
-
(2006)
J Rheumatol
, vol.33
, pp. 822-4
-
-
Travers, R.1
Allen, R.2
-
12
-
-
0035179970
-
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome
-
Nov
-
Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet 2001;29:301-5. Nov.
-
(2001)
Nat Genet
, vol.29
, pp. 301-5
-
-
Hoffman, H.M.1
Mueller, J.L.2
Broide, D.H.3
Wanderer, A.A.4
Kolodner, R.D.5
-
13
-
-
20244373040
-
Intrafamilial variable phenotypic expression of a CIAS1 mutation: From Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome
-
4
-
Hentgen V, Despert V, Leprêtre AC, Cuisset L, Chevrant-Breton J, Jégo P, Chalès G, Gall EL, Delpech M, Grateau G. Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome. J Rheumatol. 2005;32(4):747-51.
-
(2005)
J Rheumatol.
, vol.32
, pp. 747-51
-
-
Hentgen, V.1
Despert, V.2
Leprêtre, A.C.3
Cuisset, L.4
Chevrant-Breton, J.5
Jégo, P.6
Chalès, G.7
Gall, E.L.8
Delpech, M.9
Grateau, G.10
-
14
-
-
1042290321
-
Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra
-
Hawkins PN, Lachmann HJ, Aganna E, McDermott MF. Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra. Arthritis Rheum 2004;50:607-12.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 607-12
-
-
Hawkins, P.N.1
Lachmann, H.J.2
Aganna, E.3
McDermott, M.F.4
-
15
-
-
10444241090
-
Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene
-
Aróstegui JI, Aldea A, Modesto C, Rua MJ, Argüelles F, González-Enseñat MA, Ramos E, Rius J, Plaza S, Vives J, Yagüe J. Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene. Arthritis Rheum 2004;50:4045-50.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 4045-50
-
-
Aróstegui, J.I.1
Aldea, A.2
Modesto, C.3
Rua, M.J.4
Argüelles, F.5
González-Enseñat, M.A.6
Ramos, E.7
Rius, J.8
Plaza, S.9
Vives, J.10
Yagüe, J.11
-
16
-
-
34247252063
-
The clinical continuum of cryopyrinopathies: Novel CIAS1 mutations in North American patients and a new cryopyrin model
-
4
-
Aksentijevich I, D Putnam C, Remmers EF, Mueller JL, Le J, Kolodner RD, Moak Z, Chuang M, Austin F, Goldbach-Mansky R, Hoffman HM, Kastner DL. The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Arthritis Rheum 2007;56(4):1273-85.
-
(2007)
Arthritis Rheum
, vol.56
, pp. 1273-85
-
-
Aksentijevich, I.1
Putnam C, D.2
Remmers, E.F.3
Mueller, J.L.4
Le, J.5
Kolodner, R.D.6
Moak, Z.7
Chuang, M.8
Austin, F.9
Goldbach-Mansky, R.10
Hoffman, H.M.11
Kastner, D.L.12
-
17
-
-
34047120264
-
A cryopyrin-associated periodic syndrome with joint destruction
-
4
-
Lequerré T, Vittecoq O, Saugier-Veber P, Goldenberg A, Patoz P, Frébourg T, Le Loët X. A cryopyrin-associated periodic syndrome with joint destruction. Rheumatology (Oxford) 2007;46(4):709-14.
-
(2007)
Rheumatology (Oxford)
, vol.46
, pp. 709-14
-
-
Lequerré, T.1
Vittecoq, O.2
Saugier-Veber, P.3
Goldenberg, A.4
Patoz, P.5
Frébourg, T.6
Le Loët, X.7
-
19
-
-
0018745507
-
Pustulosis palmoplantaris and its relation to chronic recurrent multifocal osteomyelitis
-
Bergdahal K, Bjorksten B, Gustavson KH, et al. Pustulosis palmoplantaris and its relation to chronic recurrent multifocal osteomyelitis. Dermatologica 1979;159:37-45.
-
(1979)
Dermatologica
, vol.159
, pp. 37-45
-
-
Bergdahal, K.1
Bjorksten, B.2
Gustavson, K.H.3
-
20
-
-
0031888903
-
Chronic recurrent multifocal osteomyelitis associated with Crohn's Disease
-
Bognar M, Blake W, Agudelo C. Chronic recurrent multifocal osteomyelitis associated with Crohn's Disease. Am J Med Sci 1998;315:133-5.
-
(1998)
Am J Med Sci
, vol.315
, pp. 133-5
-
-
Bognar, M.1
Blake, W.2
Agudelo, C.3
-
21
-
-
44449163682
-
Evolution of chronic recurrent multifocal osteitis toward spondyloarthropathy over the long term
-
Vitecoq O, Said LA, Michot C, et al. Evolution of chronic recurrent multifocal osteitis toward spondyloarthropathy over the long term. Arthritis Rheum 2006;55:665-9.
-
(2006)
Arthritis Rheum
, vol.55
, pp. 665-9
-
-
Vitecoq, O.1
Said, L.A.2
Michot, C.3
-
22
-
-
33747887903
-
Conundrums in nosology: Synovitis, acne, pustulosis, hyperostosis and osteitis syndrome and spondylarthritis
-
Rohekar G, Inman RD. Conundrums in nosology: synovitis, acne, pustulosis, hyperostosis and osteitis syndrome and spondylarthritis. Arthritis Rheum 2006;55:665-9.
-
(2006)
Arthritis Rheum
, vol.55
, pp. 665-9
-
-
Rohekar, G.1
Inman, R.D.2
-
23
-
-
11844294692
-
Myocarditis and sacroileitis: Two previously unrecognized manifestations of tumor necrosis factor receptor associated periodic syndrome
-
Trost S, Rosé CD. Myocarditis and sacroileitis: two previously unrecognized manifestations of tumor necrosis factor receptor associated periodic syndrome. J Rheumatol 2005;32:175-7.
-
(2005)
J Rheumatol
, vol.32
, pp. 175-7
-
-
Trost, S.1
Rosé, C.D.2
-
24
-
-
35948985448
-
Granulomatous nephritis associated with R334Q mutation in NOD2
-
Meiorin SM, Espada G, Costa CE, et al. Granulomatous nephritis associated with R334Q mutation in NOD2. J Rheumatol 2007;34:1945-7.
-
(2007)
J Rheumatol
, vol.34
, pp. 1945-7
-
-
Meiorin, S.M.1
Espada, G.2
Costa, C.E.3
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