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Volumn 35, Issue 4, 2007, Pages 479-485

Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy

Author keywords

Electrical myotonia; Myotonia; Myotonic discharges; Myotonic dystrophy

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CORRELATION ANALYSIS; DISEASE SEVERITY; ELECTROMYOGRAPHY; FEMALE; HUMAN; HUMAN TISSUE; MALE; MUSCLE TISSUE; MUSCLE WEAKNESS; MYOTONIA; MYOTONIC DYSTROPHY; MYOTONIC DYSTROPHY TYPE 1; MYOTONIC DYSTROPHY TYPE 2; PRIORITY JOURNAL; TISSUE DISTRIBUTION;

EID: 34047219170     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.20722     Document Type: Article
Times cited : (73)

References (25)
  • 1
    • 0141780610 scopus 로고    scopus 로고
    • Glossary of terms in electrodiagnostic medicine
    • American Association of Electrodiagnostic Medicine
    • American Association of Electrodiagnostic Medicine. Glossary of terms in electrodiagnostic medicine. Muscle Nerve 2001; 26:S5-S50.
    • (2001) Muscle Nerve , vol.26
  • 3
    • 0026566108 scopus 로고
    • Molecular basis of myotonic dystrophy-expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
    • Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, et al. Molecular basis of myotonic dystrophy-expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 1992;68:799-808.
    • (1992) Cell , vol.68 , pp. 799-808
    • Brook, J.D.1    McCurrach, M.E.2    Harley, H.G.3    Buckler, A.J.4    Church, D.5    Aburatani, H.6
  • 4
    • 0036347927 scopus 로고    scopus 로고
    • Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
    • Charlet B, Savkur RS, Singh G, Philips AV, Grice EA, Cooper TA. Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. Mol Cell 2002;10:45-53.
    • (2002) Mol Cell , vol.10 , pp. 45-53
    • Charlet, B.1    Savkur, R.S.2    Singh, G.3    Philips, A.V.4    Grice, E.A.5    Cooper, T.A.6
  • 6
    • 0032995065 scopus 로고    scopus 로고
    • Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)
    • Day JW, Roelofs R, Leroy B, Pech I, Benzow K, Ranum LPW. Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2). Neuromuscul Disord 1999;9:19-27.
    • (1999) Neuromuscul Disord , vol.9 , pp. 19-27
    • Day, J.W.1    Roelofs, R.2    Leroy, B.3    Pech, I.4    Benzow, K.5    Ranum, L.P.W.6
  • 9
    • 1842476000 scopus 로고    scopus 로고
    • Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1
    • Logigian EL, Moxley RT, Blood CL, Barbieri CA, Martens WB, Wiegner AW, et al. Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1. Neurology 2004;62:1081-1089.
    • (2004) Neurology , vol.62 , pp. 1081-1089
    • Logigian, E.L.1    Moxley, R.T.2    Blood, C.L.3    Barbieri, C.A.4    Martens, W.B.5    Wiegner, A.W.6
  • 10
    • 21444450805 scopus 로고    scopus 로고
    • Clinical and molecular aspects of the myotonic dystrophies: A review
    • Machuca-Tzili L, Brook D, Hilton-Jones D. Clinical and molecular aspects of the myotonic dystrophies: a review. Muscle Nerve 2005;32:1-18.
    • (2005) Muscle Nerve , vol.32 , pp. 1-18
    • Machuca-Tzili, L.1    Brook, D.2    Hilton-Jones, D.3
  • 11
    • 0036347525 scopus 로고    scopus 로고
    • Expanded CUG repeats trigger aberrant splicing of CIC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy
    • Mankodi A, Takahashi MP, Jiang H, Beck CL, Bowers WJ, Moxley RT, et al. Expanded CUG repeats trigger aberrant splicing of CIC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy. Mol Cell 2002;10:35-44.
    • (2002) Mol Cell , vol.10 , pp. 35-44
    • Mankodi, A.1    Takahashi, M.P.2    Jiang, H.3    Beck, C.L.4    Bowers, W.J.5    Moxley, R.T.6
  • 13
    • 0028013507 scopus 로고
    • Facioscapulohumeral dystrophy natural history study-standardization of testing procedures and reliability of measurements
    • Personius KE, Pandya S, King WM, Tawil R, McDermott MP. Facioscapulohumeral dystrophy natural history study-standardization of testing procedures and reliability of measurements. Phys Ther 1994;74:253-263.
    • (1994) Phys Ther , vol.74 , pp. 253-263
    • Personius, K.E.1    Pandya, S.2    King, W.M.3    Tawil, R.4    McDermott, M.P.5
  • 14
    • 0035378594 scopus 로고    scopus 로고
    • Electrophysiological evaluation in myotonic dystrophy-correlation with CTG length expansion
    • Pfeilsticker BHM, Bertuzzo CS, Nucci A. Electrophysiological evaluation in myotonic dystrophy-correlation with CTG length expansion. Arq Neuropsiquiatr 2001;59:186-191.
    • (2001) Arq Neuropsiquiatr , vol.59 , pp. 186-191
    • Pfeilsticker, B.H.M.1    Bertuzzo, C.S.2    Nucci, A.3
  • 16
    • 0032977479 scopus 로고    scopus 로고
    • Myotonic dystrophy and proximal myotonic myopathy
    • Ricker K. Myotonic dystrophy and proximal myotonic myopathy. J Neurol 1999;246:334-338.
    • (1999) J Neurol , vol.246 , pp. 334-338
    • Ricker, K.1
  • 17
    • 0027982349 scopus 로고
    • Proximal myotonic myopathy-a new dominant disorder with myotonia, muscle weakness, and cataracts
    • Ricker K, Koch MC, Lehmann-Horn F, Pongratz D, Otto M, Heine R, et al. Proximal myotonic myopathy-a new dominant disorder with myotonia, muscle weakness, and cataracts. Neurology 1994;44:1448-1452.
    • (1994) Neurology , vol.44 , pp. 1448-1452
    • Ricker, K.1    Koch, M.C.2    Lehmann-Horn, F.3    Pongratz, D.4    Otto, M.5    Heine, R.6
  • 18
    • 0028837404 scopus 로고
    • Proximal myotonic myopathy-clinical features of a multisystem disorder similar to myotonic dystrophy
    • Ricker K, Koch MC, Lehmann-Horn F, Pongratz D, Speich N, Reiners K, et al. Proximal myotonic myopathy-clinical features of a multisystem disorder similar to myotonic dystrophy. Arch Neurol 1995;52:25-31.
    • (1995) Arch Neurol , vol.52 , pp. 25-31
    • Ricker, K.1    Koch, M.C.2    Lehmann-Horn, F.3    Pongratz, D.4    Speich, N.5    Reiners, K.6
  • 20
    • 0029804621 scopus 로고    scopus 로고
    • Heat-sensitive myotonia in proximal myotonic myopathy
    • Sander HW, Tavoulareas GP, Chokroverty S. Heat-sensitive myotonia in proximal myotonic myopathy. Neurology 1996; 47:956-962.
    • (1996) Neurology , vol.47 , pp. 956-962
    • Sander, H.W.1    Tavoulareas, G.P.2    Chokroverty, S.3
  • 21
    • 0020713021 scopus 로고
    • Electromyography in myotonic dystrophy
    • Streib E, Sun SF. Electromyography in myotonic dystrophy. Ann Neurol 1983;13:218-219.
    • (1983) Ann Neurol , vol.13 , pp. 218-219
    • Streib, E.1    Sun, S.F.2
  • 22
    • 0031034093 scopus 로고    scopus 로고
    • A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): Implications for therapeutic trials
    • The FSH-DY Group
    • The FSH-DY Group. A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): implications for therapeutic trials. Neurology 2006; 48:38-46.
    • (2006) Neurology , vol.48 , pp. 38-46
  • 23
    • 0028334933 scopus 로고
    • Myotonic dystrophy with no trinucleotide repeat expansion
    • Thornton CA, Griggs RC, Moxley RT. Myotonic dystrophy with no trinucleotide repeat expansion. Ann Neurol 1994;35: 269-272.
    • (1994) Ann Neurol , vol.35 , pp. 269-272
    • Thornton, C.A.1    Griggs, R.C.2    Moxley, R.T.3
  • 24
    • 0027957470 scopus 로고
    • Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes
    • Thornton CA, Johnson K, Moxley RT. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes. Ann Neurol 1994;35:104-107.
    • (1994) Ann Neurol , vol.35 , pp. 104-107
    • Thornton, C.A.1    Johnson, K.2    Moxley, R.T.3
  • 25
    • 0031000214 scopus 로고    scopus 로고
    • Proximal myotonic dystrophy-a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: Heterogeneity of proximal myotonic syndromes?
    • Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H. Proximal myotonic dystrophy-a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? Neuromuscul Disord 1997;7:217-228.
    • (1997) Neuromuscul Disord , vol.7 , pp. 217-228
    • Udd, B.1    Krahe, R.2    Wallgren-Pettersson, C.3    Falck, B.4    Kalimo, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.