메뉴 건너뛰기




Volumn 48, Issue 1, 1997, Pages 33-37

Proximal myotonic myopathy with MRI white matter abnormalities of the brain

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CATARACT; GENE LOCUS; HUMAN; HUMAN TISSUE; MUSCLE WEAKNESS; MYOTONIC DYSTROPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WHITE MATTER;

EID: 0031037404     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.48.1.33     Document Type: Article
Times cited : (79)

References (15)
  • 1
    • 0028334933 scopus 로고
    • Myotonic dystrophy with no trinucleotide repeat expansion
    • Thornton CA, Griggs RC, Moxley RT III. 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. III3
  • 2
    • 0027982349 scopus 로고
    • Proximal myotonic myopathy: A new dominant disorder with myotonia, muscle weakness, and cataracts
    • Ricker K, Koch MC, Lehmann-Horn F, 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
  • 3
    • 0028837404 scopus 로고
    • Proximal myotonic myopathy: Clinical features of a multisystem disorder similar to myotonic dystrophy
    • Ricker K, Koch MC, Lehmann-Horn F, 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
  • 4
    • 0029976445 scopus 로고    scopus 로고
    • Proximal myotonic myopathy: Mini-review of a recently delineated clinical disorder
    • Moxley RT III. Proximal myotonic myopathy: mini-review of a recently delineated clinical disorder. Neuromuscul Disord 1996;6:87-93.
    • (1996) Neuromuscul Disord , vol.6 , pp. 87-93
    • Moxley R.T. III1
  • 5
    • 0029040351 scopus 로고
    • Convergent myotonic dystrophy (DM) haplotypes: Potential inconsistencies in human disease gene localization
    • Whiting EJ, Tsilfidis C, Surh L, MacKenzie AE, Korneluk RG. Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization. Eur J Hum Genet 1995;3:195-202.
    • (1995) Eur J Hum Genet , vol.3 , pp. 195-202
    • Whiting, E.J.1    Tsilfidis, C.2    Surh, L.3    MacKenzie, A.E.4    Korneluk, R.G.5
  • 6
    • 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
    • published erratum appears in Cell 1992;69: 385
    • Brook JD, McCurrach ME, Harley HG, 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 [published erratum appears in Cell 1992;69: 385]. Cell 1992;68:799-808.
    • (1992) Cell , vol.68 , pp. 799-808
    • Brook, J.D.1    McCurrach, M.E.2    Harley, H.G.3
  • 8
    • 0029035545 scopus 로고
    • Lateralized differences in iodine-123-IBZM uptake in the basal ganglia in asymmetric Parkinson's disease
    • Knable MB, Jones DW, Coppola R, et al. Lateralized differences in iodine-123-IBZM uptake in the basal ganglia in asymmetric Parkinson's disease. J Nucl Med 1995;36:1216-1225.
    • (1995) J Nucl Med , vol.36 , pp. 1216-1225
    • Knable, M.B.1    Jones, D.W.2    Coppola, R.3
  • 9
    • 0029945035 scopus 로고    scopus 로고
    • A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): A challenge for future molecular studies
    • Meola G, Sansone V, Radice S, Skradski S, Ptacek L. A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies. Neuromuscul Disord 1996;6:143-150.
    • (1996) Neuromuscul Disord , vol.6 , pp. 143-150
    • Meola, G.1    Sansone, V.2    Radice, S.3    Skradski, S.4    Ptacek, L.5
  • 10
    • 0018906933 scopus 로고
    • Predominant white matter involvement in subcortical arteriosclerotic encephalopathy (Binswanger's disease)
    • Zeumer J, Schonsky B, Sturm KW. Predominant white matter involvement in subcortical arteriosclerotic encephalopathy (Binswanger's disease). J Comput Assist Tomogr 1980;4:14-19.
    • (1980) J Comput Assist Tomogr , vol.4 , pp. 14-19
    • Zeumer, J.1    Schonsky, B.2    Sturm, K.W.3
  • 11
    • 0027479304 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
    • Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet 1993;3:256-259.
    • (1993) Nat Genet , vol.3 , pp. 256-259
    • Tournier-Lasserve, E.1    Joutel, A.2    Melki, J.3
  • 12
    • 0029089247 scopus 로고
    • Clinical spectrum of CADASIL: A study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
    • Chabriat H, Vahedi K, Iba ZM, et al. Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet 1995;346:934-939.
    • (1995) Lancet , vol.346 , pp. 934-939
    • Chabriat, H.1    Vahedi, K.2    Iba, Z.M.3
  • 13
    • 0028129309 scopus 로고
    • Brain involvement in myotonic dystrophy: MRI features and their relationship to clinical and cognitive conditions
    • Censori B, Provinciali L, Danni M, et al. Brain involvement in myotonic dystrophy: MRI features and their relationship to clinical and cognitive conditions. Acta Neurol Scand 1994;90: 211-217.
    • (1994) Acta Neurol Scand , vol.90 , pp. 211-217
    • Censori, B.1    Provinciali, L.2    Danni, M.3
  • 14
    • 0028007281 scopus 로고
    • Involvement of the central nervous system in myotonic dystrophy
    • Abe K, Fujimura H, Toyooka K, et al. Involvement of the central nervous system in myotonic dystrophy. J Neurol Sci 1994;127:179-185.
    • (1994) J Neurol Sci , vol.127 , pp. 179-185
    • Abe, K.1    Fujimura, H.2    Toyooka, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.