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Volumn 48, Issue 12, 2009, Pages 1618-1619

Brain multiple sclerosis-like lesions in a patient with Muckle-Wells syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CRYOPYRIN; TRYPTOPHAN;

EID: 75649137216     PISSN: 14620324     EISSN: 14620332     Source Type: Journal    
DOI: 10.1093/rheumatology/kep321     Document Type: Letter
Times cited : (28)

References (7)
  • 1
    • 73649189052 scopus 로고
    • Urticaria, deafness, and amyloidosis: A new heredo-familial syndrome
    • Muckle TJ, Wells M. Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome. Q J Med 1962;31:235-48.
    • (1962) Q J Med , vol.31 , pp. 235-248
    • Muckle, T.J.1    Wells, M.2
  • 2
    • 0035179970 scopus 로고    scopus 로고
    • Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome
    • 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.
    • (2001) Nat Genet , vol.29 , pp. 301-305
    • Hoffman, H.M.1    Mueller, J.L.2    Broide, D.H.3    Wanderer, A.A.4    Kolodner, R.D.5
  • 3
    • 34047120264 scopus 로고    scopus 로고
    • A cryopyrin-associated periodic syndrome with joint destruction
    • Lequerre T, Vittecoq O, Saugier-Veber P et al. A cryopyrin-associated periodic syndrome with joint destruction. Rheumatology 2007;46:709-14.
    • (2007) Rheumatology , vol.46 , pp. 709-714
    • Lequerre, T.1    Vittecoq, O.2    Saugier-Veber, P.3
  • 4
    • 20244373040 scopus 로고    scopus 로고
    • Intrafamilial variable phenotypic expression of a CIAS1 mutation: From Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome
    • Hentgen V, Despert V, Lepretre AC et al. Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome. J Rheumatol 2005;32:747-51.
    • (2005) J Rheumatol , vol.32 , pp. 747-751
    • Hentgen, V.1    Despert, V.2    Lepretre, A.C.3
  • 5
    • 0037251380 scopus 로고    scopus 로고
    • CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes
    • Granel B, Philip N, Serratrice J et al. CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes. Dermatology 2003;206:257-9.
    • (2003) Dermatology , vol.206 , pp. 257-259
    • Granel, B.1    Philip, N.2    Serratrice, J.3
  • 6
    • 34547747790 scopus 로고    scopus 로고
    • Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation
    • Kumpfel T, Hoffmann LA, Rubsamen H et al. Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation. Arthritis Rheum 2007;56:2774-83.
    • (2007) Arthritis Rheum , vol.56 , pp. 2774-2783
    • Kumpfel, T.1    Hoffmann, L.A.2    Rubsamen, H.3
  • 7
    • 34548675581 scopus 로고    scopus 로고
    • The NLR network and the immunological disease continuum of adaptive and innate immune-mediated inflammation against self
    • McGonagle D, Savic S, McDermott MF. The NLR network and the immunological disease continuum of adaptive and innate immune-mediated inflammation against self. Semin Immunopathol 2007;29:303-13.
    • (2007) Semin Immunopathol , vol.29 , pp. 303-313
    • McGonagle, D.1    Savic, S.2    McDermott, M.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.