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Volumn 12, Issue 2, 2005, Pages 160-161

Proximal myotonic dystrophy mimicking progressive muscular atrophy [2]

Author keywords

Myotonic dystrophies; Progressive muscular atrophy; Proximal myotonic dystrophy; Proximal myotonic myopathy

Indexed keywords

AGED; BICEPS BRACHII MUSCLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC ERROR; ELECTROMYOGRAPHY; FACE MUSCLE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HUMAN; IMMUNOHISTOCHEMISTRY; LETTER; MALE; MUSCLE ATROPHY; MUSCLE CELL; MUSCLE WEAKNESS; MYOTONIC DYSTROPHY; PRIORITY JOURNAL; PROXIMAL MYOTONIC DYSTROPHY; TENDON REFLEX;

EID: 13844310348     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2004.01032.x     Document Type: Letter
Times cited : (6)

References (9)
  • 1
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    • Myotonic dystrophy type 2: Molecular, diagnostic and clinical spectrum
    • Day JW, Ricker K, Jacobsen JF et al. (2003). Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum. Neurology 60:657-664.
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    • Day, J.W.1    Ricker, K.2    Jacobsen, J.F.3
  • 2
    • 0035800434 scopus 로고    scopus 로고
    • Myotonic dystrophy type 2 caused a CCTG expansion in intron 1 of ZNF9
    • Liquori CL, Ricker K, Moseley LM et al. (2001). Myotonic dystrophy type 2 caused a CCTG expansion in intron 1 of ZNF9. Science 293:864-867.
    • (2001) Science , vol.293 , pp. 864-867
    • Liquori, C.L.1    Ricker, K.2    Moseley, L.M.3
  • 3
    • 0036169578 scopus 로고    scopus 로고
    • Report of the 84th ENMC Workshop: PROMM (Proximal Myotonic Myopathy) and other Myotonic Dystrophy-like Syndromes
    • Moxley RT III Meola G, Udd B, Ricker K (2002). Report of the 84th ENMC Workshop: PROMM (Proximal Myotonic Myopathy) and other Myotonic Dystrophy-like Syndromes. Neuromuscul Disord 12:306-317.
    • (2002) Neuromuscul Disord , vol.12 , pp. 306-317
    • Moxley III, R.T.1    Meola, G.2    Udd, B.3    Ricker, K.4
  • 5
    • 12144286209 scopus 로고    scopus 로고
    • New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)
    • Sallinen R, Vihola A, Bachinski LL et al. (2004). New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscul Disord 14:274-283.
    • (2004) Neuromuscul Disord , vol.14 , pp. 274-283
    • Sallinen, R.1    Vihola, A.2    Bachinski, L.L.3
  • 6
    • 0034992228 scopus 로고    scopus 로고
    • Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes
    • Schneider C, Wessig C, Muller CR, Brechtelsbauer D, Grimm T (2001). Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromes. Neuromuscul Disord 11:485-488.
    • (2001) Neuromuscul Disord , vol.11 , pp. 485-488
    • Schneider, C.1    Wessig, C.2    Muller, C.R.3    Brechtelsbauer, D.4    Grimm, T.5
  • 7
    • 0031000214 scopus 로고    scopus 로고
    • Proximal myotonic dystrophy - A family with autosomal dominant muscular dystrophy, cataracts, hearing loss, and hypogonadism - Heterogeneity of proximal myotonic disorders
    • Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H (1997). Proximal myotonic dystrophy - a family with autosomal dominant muscular dystrophy, cataracts, hearing loss, and hypogonadism - heterogeneity of proximal myotonic disorders. Neuromuscul Disord 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
  • 8
    • 0043073111 scopus 로고    scopus 로고
    • Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies
    • Udd B, Meola G, Krahe R et al. (2003). Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. Neuromuscul Disord 13:589-596.
    • (2003) Neuromuscul Disord , vol.13 , pp. 589-596
    • Udd, B.1    Meola, G.2    Krahe, R.3
  • 9
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    • Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2
    • Vihola A, Bassez G, Meola G et al. (2003). Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology 60:1854-1857.
    • (2003) Neurology , vol.60 , pp. 1854-1857
    • Vihola, A.1    Bassez, G.2    Meola, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.