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Volumn 19, Issue 2, 2009, Pages 167-171

Eosinophilic myositis as presenting symptom in γ-sarcoglycanopathy

Author keywords

Sarcoglycanopathy; Eosinophilic myositis; LGMD2C; Limb girdle muscular dystrophy

Indexed keywords

CALCIUM; COLECALCIFEROL; CORTICOSTEROID; GAMMA SARCOGLYCAN; PREDNISOLONE;

EID: 59249092358     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2008.11.010     Document Type: Article
Times cited : (29)

References (16)
  • 1
    • 36249024105 scopus 로고    scopus 로고
    • EFNS Guideline Task Force. EFNS guideline on diagnosis and management of limb girdle muscular dystrophies
    • Norwood F., deVisser M., Eymard B., Lochmüller H., and Bushby K. EFNS Guideline Task Force. EFNS guideline on diagnosis and management of limb girdle muscular dystrophies. Eur J Neurol 14 12 (2007) 1305-1312
    • (2007) Eur J Neurol , vol.14 , Issue.12 , pp. 1305-1312
    • Norwood, F.1    deVisser, M.2    Eymard, B.3    Lochmüller, H.4    Bushby, K.5
  • 2
    • 0025292555 scopus 로고
    • Fasciitis, perimyositis, myositis, polymyositis and eosinophilia
    • Serratrice G., Pellissier J.F., Roux H., and Quilichini P. Fasciitis, perimyositis, myositis, polymyositis and eosinophilia. Muscle Nerve 13 (1990) 385-395
    • (1990) Muscle Nerve , vol.13 , pp. 385-395
    • Serratrice, G.1    Pellissier, J.F.2    Roux, H.3    Quilichini, P.4
  • 3
    • 33744792021 scopus 로고    scopus 로고
    • CAPN3 mutations in patients with idiopathic eosinophilic myositis
    • Krahn M., Lopez de Munain A., Streichenberger N., et al. CAPN3 mutations in patients with idiopathic eosinophilic myositis. Ann Neurol 59 6 (2006) 905-911
    • (2006) Ann Neurol , vol.59 , Issue.6 , pp. 905-911
    • Krahn, M.1    Lopez de Munain, A.2    Streichenberger, N.3
  • 4
    • 33744831966 scopus 로고    scopus 로고
    • Calpainopathy and eosinophilic myositis
    • Brown Jr. R.H., and Amato A. Calpainopathy and eosinophilic myositis. Ann Neurol 59 (2006) 875-877
    • (2006) Ann Neurol , vol.59 , pp. 875-877
    • Brown Jr., R.H.1    Amato, A.2
  • 5
    • 40349113027 scopus 로고    scopus 로고
    • Adults with eosinophilic myositis and calpain-3 mutations
    • Feb 26
    • Amato A.A. Adults with eosinophilic myositis and calpain-3 mutations. Neurology 70 9 (2008) 730-731 Feb 26
    • (2008) Neurology , vol.70 , Issue.9 , pp. 730-731
    • Amato, A.A.1
  • 6
    • 0030965486 scopus 로고    scopus 로고
    • Becker muscular dystrophy presenting as eosinophilic inflammatory myopathy in an infant
    • Weinstock A., Green C., Cohen B.H., and Prayson R.A. Becker muscular dystrophy presenting as eosinophilic inflammatory myopathy in an infant. J Child Neurol 12 2 (1997) 146-147
    • (1997) J Child Neurol , vol.12 , Issue.2 , pp. 146-147
    • Weinstock, A.1    Green, C.2    Cohen, B.H.3    Prayson, R.A.4
  • 7
    • 0141815578 scopus 로고    scopus 로고
    • Calpain 3 cleaves filamin c and regulates its ability to interact with gama- and delta-sarcoglycans
    • Guyon J.R., Kudryashova E., Potts A., et al. Calpain 3 cleaves filamin c and regulates its ability to interact with gama- and delta-sarcoglycans. Muscle Nerve 28 (2003) 472-483
    • (2003) Muscle Nerve , vol.28 , pp. 472-483
    • Guyon, J.R.1    Kudryashova, E.2    Potts, A.3
  • 8
    • 0028961960 scopus 로고
    • Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses
    • Arahata K., Ishihara T., Fukunaga H., et al. Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses. Muscle Nerve 2 (1995) 56-66
    • (1995) Muscle Nerve , vol.2 , pp. 56-66
    • Arahata, K.1    Ishihara, T.2    Fukunaga, H.3
  • 9
    • 10544230641 scopus 로고    scopus 로고
    • Congenital muscular dystrophy with primary laminin alpha 2 (merosin) deficiency presenting as inflammatory myopathy
    • Pegoraro E., Mancias P., Swerdlow S.H., et al. Congenital muscular dystrophy with primary laminin alpha 2 (merosin) deficiency presenting as inflammatory myopathy. Ann Neurol 40 5 (1996) 782-791
    • (1996) Ann Neurol , vol.40 , Issue.5 , pp. 782-791
    • Pegoraro, E.1    Mancias, P.2    Swerdlow, S.H.3
  • 10
    • 0032884692 scopus 로고    scopus 로고
    • Prominent inflammatory changes on muscle biopsy in patients with Myoshi myopathy
    • Rowin J., Meriggioli M.N., Cochran E.J., and Sanders D.B. Prominent inflammatory changes on muscle biopsy in patients with Myoshi myopathy. Neuromuscul Disord 9 6-7 (1999) 417-420
    • (1999) Neuromuscul Disord , vol.9 , Issue.6-7 , pp. 417-420
    • Rowin, J.1    Meriggioli, M.N.2    Cochran, E.J.3    Sanders, D.B.4
  • 11
    • 0034709195 scopus 로고    scopus 로고
    • Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation
    • McNally E., Ly C.T., Rosenmann H., et al. Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation. Am J Med Gen 91 (2000) 305-312
    • (2000) Am J Med Gen , vol.91 , pp. 305-312
    • McNally, E.1    Ly, C.T.2    Rosenmann, H.3
  • 12
    • 0035846620 scopus 로고    scopus 로고
    • Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients
    • Dec 11
    • Gallardo E., Rojas-Garcia R., de Luna N., Pou A., Brown Jr. R.H., and Illa I. Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients. Neurology 57 11 (2001) 2136-2138 Dec 11
    • (2001) Neurology , vol.57 , Issue.11 , pp. 2136-2138
    • Gallardo, E.1    Rojas-Garcia, R.2    de Luna, N.3    Pou, A.4    Brown Jr., R.H.5    Illa, I.6
  • 13
    • 33845292617 scopus 로고    scopus 로고
    • Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy
    • Godfrey C., Escolar D., Brockington M., et al. Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy. Ann Neurol 60 (2006) 603-610
    • (2006) Ann Neurol , vol.60 , pp. 603-610
    • Godfrey, C.1    Escolar, D.2    Brockington, M.3
  • 15
    • 35148838187 scopus 로고    scopus 로고
    • POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes
    • Nov 30
    • Biancheri R., Falace A., Tessa A., et al. POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. Biochem Biophys Res Commun 363 4 (2007) 1033-1037 Nov 30
    • (2007) Biochem Biophys Res Commun , vol.363 , Issue.4 , pp. 1033-1037
    • Biancheri, R.1    Falace, A.2    Tessa, A.3
  • 16
    • 0033838714 scopus 로고    scopus 로고
    • Eosinophilia of dystrophin-deficient muscle is promoted by perforin-mediated cytotoxicity by T cell effectors
    • Cai B., Spencer M.J., Nakamura G., Tseng-Ong L., and Tidball J.G. Eosinophilia of dystrophin-deficient muscle is promoted by perforin-mediated cytotoxicity by T cell effectors. Am J Pathol 156 5 (2000) 1789-1796
    • (2000) Am J Pathol , vol.156 , Issue.5 , pp. 1789-1796
    • Cai, B.1    Spencer, M.J.2    Nakamura, G.3    Tseng-Ong, L.4    Tidball, J.G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.