-
1
-
-
66649102432
-
Canakinumab in CAPS Study Group Use of canakinumab in the cryopyrin-associated periodic syndrome
-
LACHMANN HJ, KONE-PAUT I, KUEMMERLE-DESCHNER JB et al. Canakinumab in CAPS Study Group. Use of canakinumab in the cryopyrin-associated periodic syndrome. N Engl J Med 2009; 360: 2416-25.
-
(2009)
N Engl J Med
, vol.360
, pp. 2416-2425
-
-
Lachmann, H.J.1
Kone-Paut, I.2
Kuemmerle-Deschner, J.B.3
-
2
-
-
79551533377
-
Cryopyrin-associated periodic syndrome: an update on diagnosis and treatment response
-
YU JR, LESLIE KS Cryopyrin-associated periodic syndrome: an update on diagnosis and treatment response. Curr Allergy Asthma Rep 2011; 11: 12-20.
-
(2011)
Curr Allergy Asthma Rep
, vol.11
, pp. 12-20
-
-
Yu, J.R.1
Leslie, K.S.2
-
3
-
-
84856571891
-
Bridging the gap between the clinician and the patient with cryopyrin-associated periodic syndromes
-
CANTARINI L, LUCHERINI OM, FREDIANI B et al. Bridging the gap between the clinician and the patient with cryopyrin-associated periodic syndromes. Int J Immunopathol Pharmacol 2011; 24: 827-26.
-
(2011)
Int J Immunopathol Pharmacol
, vol.24
, pp. 827-926
-
-
Cantarini, L.1
Lucherini, O.M.2
Frediani, B.3
-
4
-
-
65649100204
-
Neurological manifestations of the Mendelian-inherited autoinflammatory syndromes
-
MONTEALEGRE SANCHEZ GA, HASHKES PJ Neurological manifestations of the Mendelian-inherited autoinflammatory syndromes. Dev Med Child Neurol 2009; 51: 420-8.
-
(2009)
Dev Med Child Neurol
, vol.51
, pp. 420-428
-
-
Montealegre Sanchez, G.A.1
Hashkes, P.J.2
-
5
-
-
0034774916
-
Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever
-
HOFFMAN HM, WANDERER AA, BROIDE DH Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever. J Allergy Clin Immunol 2001; 108: 615-20.
-
(2001)
J Allergy Clin Immunol
, vol.108
, pp. 615-620
-
-
Hoffman, H.M.1
Wanderer, A.A.2
Broide, D.H.3
-
6
-
-
38049083888
-
Primer: inflammasomes and interleukin 1beta in inflammatory disorders
-
CHURCH LD, COOK GP, MCDERMOTT MF Primer: inflammasomes and interleukin 1beta in inflammatory disorders. Nat Clin Pract Rheumatol 2008; 4: 34-42.
-
(2008)
Nat Clin Pract Rheumatol
, vol.4
, pp. 34-42
-
-
Church, L.D.1
Cook, G.P.2
Mcdermott, M.F.3
-
7
-
-
33746876396
-
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition
-
GOLDBACH-MANSKY R, DAILEY NJ, CANNA SW et al. Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition. N Engl J Med 2006; 355: 581-92.
-
(2006)
N Engl J Med
, vol.355
, pp. 581-592
-
-
Goldbach-Mansky, R.1
Dailey, N.J.2
Canna, S.W.3
-
8
-
-
12144288979
-
Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU
-
NEVEN B, CALLEBAUT I, PRIEUR AM et al. Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU. Blood 2004; 103: 2809-15.
-
(2004)
Blood
, vol.103
, pp. 2809-2815
-
-
Neven, B.1
Callebaut, I.2
Prieur, A.M.3
-
9
-
-
18344385660
-
New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes
-
DODÉ C, LE DÛ N, CUISSET L et al. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes. Am J Hum Genet 2002; 70: 1498-506.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1498-1506
-
-
Dodé, C.1
Le Dû, N.2
Cuisset, L.3
-
10
-
-
34247252063
-
The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model
-
AKSENTIJEVICH I, D PUTNAM C, REMMERS EF et al. The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Arthritis Rheum 2007; 56: 1273-85.
-
(2007)
Arthritis Rheum
, vol.56
, pp. 1273-1285
-
-
Aksentijevichi, D.1
Putnam, C.2
Remmers, E.F.3
-
11
-
-
0037317936
-
Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation L353P
-
HOFFMAN HM, GREGORY SG, MUELLER JL et al. Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P. Hum Genet 2003; 112: 209-16.
-
(2003)
Hum Genet
, vol.112
, pp. 209-216
-
-
Hoffman, H.M.1
Gregory, S.G.2
Mueller, J.L.3
-
12
-
-
40549084310
-
Gene polymorphisms in the NALP3 inflammasome are associated with interleukin-1 production and severe inflammation: relation to common inflammatory diseases?
-
VERMA D, LERM M, BLOMGRAN JULINDER R, ERIKSSON P, SÖDERKVIST P, SÄRNDAHL E Gene polymorphisms in the NALP3 inflammasome are associated with interleukin-1 production and severe inflammation: relation to common inflammatory diseases? Arthritis Rheum 2008; 58: 888-94
-
(2008)
Arthritis Rheum
, vol.58
, pp. 888-894
-
-
Verma, D.1
Lerm, M.2
Blomgran Julinder, R.3
Eriksson, P.4
Söderkvist, P.5
Särndahl, E.6
-
13
-
-
4143125654
-
Infevers: an evolving mutation database for auto-inflammatory syndromes
-
TOUITOU I, LESAGE S, MCDERMOTT M et al. Infevers: an evolving mutation database for auto-inflammatory syndromes. Hum Mutat 2004; 24: 194-8.
-
(2004)
Hum Mutat
, vol.24
, pp. 194-198
-
-
Touitou, I.1
Lesage, S.2
Mcdermott, M.3
-
14
-
-
34248185606
-
Nonclassic neurologic features in cryopyrin-associated periodic syndromes
-
TING TV, SCALZI LV, HASHKES PJ Nonclassic neurologic features in cryopyrin-associated periodic syndromes. Pediatr Neurol 2007; 36: 338-41.
-
(2007)
Pediatr Neurol
, vol.36
, pp. 338-341
-
-
Ting, T.V.1
Scalzi, L.V.2
Hashkes, P.J.3
-
15
-
-
77955291693
-
Followup and quality of life of patients with cryopyrin-associated periodic syndromes treated with Anakinra
-
LEPORE L, PALONI G, CAORSI R et al. Followup and quality of life of patients with cryopyrin-associated periodic syndromes treated with Anakinra. J Pediatr 2010; 157: 310-5.
-
(2010)
J Pediatr
, vol.157
, pp. 310-315
-
-
Lepore, L.1
Paloni, G.2
Caorsi, R.3
-
16
-
-
0036745064
-
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis
-
AGANNA E, MARTINON F, HAWKINS PN et al. Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis. Arthritis Rheum 2002; 46: 2445-52.
-
(2002)
Arthritis Rheum
, vol.46
, pp. 2445-2452
-
-
Aganna, E.1
Martinon, F.2
Hawkins, P.N.3
-
17
-
-
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 et al. 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. 4045-4050
-
-
Aróstegui, J.I.1
Aldea, A.2
Modesto, C.3
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