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Volumn 8, Issue 7, 1998, Pages 459-466

Autosomal dominant late adult onset distal leg myopathy

Author keywords

Autosomal dominant inheritance; Distal myopathy; Immunocytochemistry; Inclusion body myopathy

Indexed keywords

CREATINE KINASE;

EID: 0032191687     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(98)00063-7     Document Type: Article
Times cited : (21)

References (23)
  • 1
    • 0029011231 scopus 로고
    • Distal myopathies
    • Workshop report from 25th ENMC International Workshop, 18-20 November 1994, Naarden, the Netherlands
    • [1] Somer H. Distal myopathies. Workshop report from 25th ENMC International Workshop, 18-20 November 1994, Naarden, the Netherlands. Neuromusc Disord 1995;5:249-252.
    • (1995) Neuromusc Disord , vol.5 , pp. 249-252
    • Somer, H.1
  • 2
    • 0003132648 scopus 로고
    • Myopathia distalis tarda hereditaria
    • [2] Welander L. Myopathia distalis tarda hereditaria. Acta Med Scand 1951;141:1-124.
    • (1951) Acta Med Scand , vol.141 , pp. 1-124
    • Welander, L.1
  • 4
    • 0027278526 scopus 로고
    • Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients
    • [4] Udd B, Partanen J, Halonen P, et al. Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients. Arch Neurol 1993;50:604-608.
    • (1993) Arch Neurol , vol.50 , pp. 604-608
    • Udd, B.1    Partanen, J.2    Halonen, P.3
  • 5
    • 0022634885 scopus 로고
    • Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy: Seventeen cases in eight families including an autopsied case
    • [5] Miyoshi K, Kawai H, Iwasa M, Kusaka K, Nishino H. Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy: seventeen cases in eight families including an autopsied case. Brain 1986;109:31-54.
    • (1986) Brain , vol.109 , pp. 31-54
    • Miyoshi, K.1    Kawai, H.2    Iwasa, M.3    Kusaka, K.4    Nishino, H.5
  • 6
    • 0019481203 scopus 로고
    • Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
    • [6] Nonaka I, Sunohara N, Ishiura S, Satayoshi E. Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 1981;51:141-155.
    • (1981) J Neurol Sci , vol.51 , pp. 141-155
    • Nonaka, I.1    Sunohara, N.2    Ishiura, S.3    Satayoshi, E.4
  • 7
    • 0000114741 scopus 로고
    • Distal myopathies
    • Engel AG, Franzini-Armstrong C, editors. New York: McGraw-Hill
    • [7] Griggs RC, Markesbery WR. Distal myopathies. In: Engel AG, Franzini-Armstrong C, editors. Myology, second ed, New York: McGraw-Hill, 1994:1246-1257.
    • (1994) Myology, Second Ed , pp. 1246-1257
    • Griggs, R.C.1    Markesbery, W.R.2
  • 8
    • 0028951204 scopus 로고
    • Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
    • [8] Bejaoui K, Hirabayashi K, Hentati F, et al. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology 1995;45:768-772.
    • (1995) Neurology , vol.45 , pp. 768-772
    • Bejaoui, K.1    Hirabayashi, K.2    Hentati, F.3
  • 9
    • 0028326542 scopus 로고
    • A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p
    • [9] Bashir R, Strachan T, Keers S, et al. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum Mol Genet 1994;3:455-457.
    • (1994) Hum Mol Genet , vol.3 , pp. 455-457
    • Bashir, R.1    Strachan, T.2    Keers, S.3
  • 10
    • 0021320516 scopus 로고
    • 'Rimmed vacuole myopathy' sparing the quadriceps: A unique disorder in Iranian Jews
    • [10] Argov Z, Yarom R. 'Rimmed vacuole myopathy' sparing the quadriceps: a unique disorder in Iranian Jews. J Neurol Sci 1984;64:33-43.
    • (1984) J Neurol Sci , vol.64 , pp. 33-43
    • Argov, Z.1    Yarom, R.2
  • 11
    • 0030933296 scopus 로고    scopus 로고
    • Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9
    • [11] Ikeuchi T, Asaka T, Saito M, et al. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9. Ann Neurol 1997;41:432-437.
    • (1997) Ann Neurol , vol.41 , pp. 432-437
    • Ikeuchi, T.1    Asaka, T.2    Saito, M.3
  • 12
    • 0030063986 scopus 로고    scopus 로고
    • Hereditary inclusion body myopathy maps to chromosome 9p1-q1
    • [12] Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, et al. Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Hum Mol Genet 1996;5:159-163.
    • (1996) Hum Mol Genet , vol.5 , pp. 159-163
    • Mitrani-Rosenbaum, S.1    Argov, Z.2    Blumenfeld, A.3
  • 14
    • 0017687587 scopus 로고
    • Distal myopathy: Electron microscopic and histochemical studies
    • [14] Markesbery WR, Griggs RC, Herr B. Distal myopathy: electron microscopic and histochemical studies. Neurology 1977;27:727-735.
    • (1977) Neurology , vol.27 , pp. 727-735
    • Markesbery, W.R.1    Griggs, R.C.2    Herr, B.3
  • 15
    • 0028787389 scopus 로고
    • Inclusion body myositis and myopathies
    • [15] Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol 1995;38:705-713.
    • (1995) Ann Neurol , vol.38 , pp. 705-713
    • Griggs, R.C.1    Askanas, V.2    Dimauro, S.3
  • 16
    • 0008139317 scopus 로고    scopus 로고
    • Inclusion body myopathies
    • Askanas V, Serratrice G, Engel WK, editors. Cambridge University Press (in press)
    • [16] Fardeau M, Tome FMS. Inclusion body myopathies. In: Askanas V, Serratrice G, Engel WK, editors. Inclusion body myositis and myopathies, Cambridge University Press (in press).
    • Inclusion Body Myositis and Myopathies
    • Fardeau, M.1    Tome, F.M.S.2
  • 17
    • 0010309911 scopus 로고
    • Hereditary neuromuscular disorder with inclusion body myositis-like filamentous inclusions: Clinical, pathological and tissue culture
    • [17] Fardeau M, Askanas V, Tomé FMS, Engel KW, Alvarez RB, Chevallay M. Hereditary neuromuscular disorder with inclusion body myositis-like filamentous inclusions: clinical, pathological and tissue culture. Neurology 1990;40(Suppl 1):120.
    • (1990) Neurology , vol.40 , Issue.SUPPL. 1 , pp. 120
    • Fardeau, M.1    Askanas, V.2    Tomé, F.M.S.3    Engel, K.W.4    Alvarez, R.B.5    Chevallay, M.6
  • 19
    • 0000780231 scopus 로고
    • 'Familial inclusion body myositis' sparing the quadriceps with asymptomatic leukoencephalopathy in a Tunisian kindred
    • [19] Hentati F, Ben Hamida C, Tomé F, Oueslati S, Fardeau M, Ben Hamida M. 'Familial inclusion body myositis' sparing the quadriceps with asymptomatic leukoencephalopathy in a Tunisian kindred. Neurology 1991;41(Suppl 1):422.
    • (1991) Neurology , vol.41 , Issue.SUPPL. 1 , pp. 422
    • Hentati, F.1    Ben Hamida, C.2    Tomé, F.3    Oueslati, S.4    Fardeau, M.5    Ben Hamida, M.6
  • 20
    • 0027407477 scopus 로고
    • Vacuolar myopathy sparing the quadriceps
    • [20] Sadeh M, Gadoth M, Hadar H, Ben David E. Vacuolar myopathy sparing the quadriceps. Brain 1993;16:217-232.
    • (1993) Brain , vol.16 , pp. 217-232
    • Sadeh, M.1    Gadoth, M.2    Hadar, H.3    Ben David, E.4
  • 21
    • 0026609582 scopus 로고
    • Familial inclusion body myositis: Evidence for autosomal dominant inheritance
    • [21] Neville HE, Baumbach LL, Ringel SP, et al. Familial inclusion body myositis: evidence for autosomal dominant inheritance. Neurology 1992;42:897-902.
    • (1992) Neurology , vol.42 , pp. 897-902
    • Neville, H.E.1    Baumbach, L.L.2    Ringel, S.P.3
  • 22
    • 0029826654 scopus 로고    scopus 로고
    • The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps sparing phenotype in non-Iranian Jews
    • [22] Sivakumar K, Dalakas MC. The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps sparing phenotype in non-Iranian Jews. Neurology 1996;47:977-984.
    • (1996) Neurology , vol.47 , pp. 977-984
    • Sivakumar, K.1    Dalakas, M.C.2
  • 23
    • 0031979926 scopus 로고    scopus 로고
    • Assignment of the tibial muscular dystrophy locus to chromosome 2q31
    • [23] Haravuori H, Mäkelä-Bengs P, Udd B, et al. Assignment of the tibial muscular dystrophy locus to chromosome 2q31. Am J Hum Genet 1998;62:620-626.
    • (1998) Am J Hum Genet , vol.62 , pp. 620-626
    • Haravuori, H.1    Mäkelä-Bengs, P.2    Udd, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.