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Volumn 7, Issue 3, 1997, Pages 191-197

Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

Author keywords

Basal lamina; Electron microscopy; Fukuyama congenital muscular dystrophy

Indexed keywords

ARTICLE; BASEMENT MEMBRANE; CELL MEMBRANE; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTRON MICROSCOPY; FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; HUMAN; HUMAN TISSUE; IMMUNOCYTOCHEMISTRY; MUSCLE CELL; MUSCULAR DYSTROPHY; PRIORITY JOURNAL; SKELETAL MUSCLE;

EID: 0030982138     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(97)00462-8     Document Type: Article
Times cited : (56)

References (46)
  • 1
    • 0001916852 scopus 로고
    • Muscular dystrophies
    • Dubowitz V, editor. London, UK: WB Saunders
    • Dubowitz V. Muscular dystrophies. In: Dubowitz V, editor. Muscle Disorders in Childhood. London, UK: WB Saunders, 1995:34-133.
    • (1995) Muscle Disorders in Childhood , pp. 34-133
    • Dubowitz, V.1
  • 2
  • 3
    • 0001874191 scopus 로고
    • Congenital muscular dyslrophy
    • Vinken PJ, Bruyn GW, editors. Amsterdam: North-Holland
    • Nonaka I, Chou SM. Congenital muscular dyslrophy. In: Vinken PJ, Bruyn GW, editors. Handbook of Clinical Neurology. Amsterdam: North-Holland, 1979:27-50.
    • (1979) Handbook of Clinical Neurology , pp. 27-50
    • Nonaka, I.1    Chou, S.M.2
  • 4
    • 0002618558 scopus 로고
    • A peculiar form of congenital progressive muscular dystrophy
    • Fukuyama Y, Kawazura M, Haruna H. A peculiar form of congenital progressive muscular dystrophy. Paediatr Univ Tokyo 1960;4:5-8.
    • (1960) Paediatr Univ Tokyo , vol.4 , pp. 5-8
    • Fukuyama, Y.1    Kawazura, M.2    Haruna, H.3
  • 5
    • 0024539092 scopus 로고
    • Diagnostic criteria for Walker-Warburg syndrome
    • Dobyns WB, Pagon RA, Armstrong D, et al. Diagnostic criteria for Walker-Warburg syndrome. Am J Med Genet 1989;32:195-210.
    • (1989) Am J Med Genet , vol.32 , pp. 195-210
    • Dobyns, W.B.1    Pagon, R.A.2    Armstrong, D.3
  • 6
    • 0000644417 scopus 로고
    • Muscle, eye and brain disease: A new syndrome
    • Santavuori P, Leisti J, Kraus S. Muscle, eye and brain disease: a new syndrome (abstract). Neuropaediatrie 1977;8(Suppl):553.
    • (1977) Neuropaediatrie , vol.8 , Issue.SUPPL. , pp. 553
    • Santavuori, P.1    Leisti, J.2    Kraus, S.3
  • 9
    • 0028094441 scopus 로고
    • Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
    • Hillaire D, Leclerc A, Fauré S, et al. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Hum Mol Genet 1994;3:1657-61.
    • (1994) Hum Mol Genet , vol.3 , pp. 1657-1661
    • Hillaire, D.1    Leclerc, A.2    Fauré, S.3
  • 10
    • 0029102340 scopus 로고
    • Deficiency of laminin alpha 2- Chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy
    • Hayashi YK, Koga R, Tsukahara T, et al. Deficiency of laminin alpha 2- chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy. Muscle Nerve 1995;18:1027-30.
    • (1995) Muscle Nerve , vol.18 , pp. 1027-1030
    • Hayashi, Y.K.1    Koga, R.2    Tsukahara, T.3
  • 11
    • 0028980027 scopus 로고
    • Mutations in the laminin α2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
    • Helbling-Leclerc A, Zhang X, Topaloglu H, et al. Mutations in the laminin α2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nature Genet 1995;11:216-18.
    • (1995) Nature Genet , vol.11 , pp. 216-218
    • Helbling-Leclerc, A.1    Zhang, X.2    Topaloglu, H.3
  • 12
    • 0019471880 scopus 로고
    • Congenital progressive muscular dystrophy of the Fukuyama type: Clinical genetic and pathologic considerations
    • Fukuyama Y, Osawa M, Suzuki H. Congenital progressive muscular dystrophy of the Fukuyama type: clinical genetic and pathologic considerations. Brain Dev (Tokyo) 1981;13:1-29.
    • (1981) Brain Dev (Tokyo) , vol.13 , pp. 1-29
    • Fukuyama, Y.1    Osawa, M.2    Suzuki, H.3
  • 13
    • 0017123442 scopus 로고
    • Congenital muscular dystrophy as a disease of the central nervous system
    • Kamoshita S, Konishi Y, Segawa M, Fukuyama Y. Congenital muscular dystrophy as a disease of the central nervous system. Arch Neurol 1976;33:513-6.
    • (1976) Arch Neurol , vol.33 , pp. 513-516
    • Kamoshita, S.1    Konishi, Y.2    Segawa, M.3    Fukuyama, Y.4
  • 15
    • 0021136592 scopus 로고
    • Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type)
    • Takada K, Nakamura H, Tanaka J. Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type). J Neuropathol Exp Neurol 1984;43:395-407.
    • (1984) J Neuropathol Exp Neurol , vol.43 , pp. 395-407
    • Takada, K.1    Nakamura, H.2    Tanaka, J.3
  • 16
    • 0023231444 scopus 로고
    • Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD)
    • Takada K, Nakamura H, Suzumori K, Ishikawa T, Sugiyama N. Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD). Acta Neuropathol 1987;74:300-6.
    • (1987) Acta Neuropathol , vol.74 , pp. 300-306
    • Takada, K.1    Nakamura, H.2    Suzumori, K.3    Ishikawa, T.4    Sugiyama, N.5
  • 17
    • 0030031292 scopus 로고    scopus 로고
    • Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? - Pathological study of the cerebral cortex of an FCMD fetus
    • Nakano I, Funahashi M, Takada K, Toda T. Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? - Pathological study of the cerebral cortex of an FCMD fetus. Acta Neuropathol 1996;91:313-21.
    • (1996) Acta Neuropathol , vol.91 , pp. 313-321
    • Nakano, I.1    Funahashi, M.2    Takada, K.3    Toda, T.4
  • 18
    • 84996350040 scopus 로고
    • Histological, histochemical and electron microscopical studies of biopsied muscle of congenital muscular dystrophy (arthrogrypotic type congenital muscular dystrophy with mental retardation and facial muscle involvement)
    • Segawa M. Histological, histochemical and electron microscopical studies of biopsied muscle of congenital muscular dystrophy (arthrogrypotic type congenital muscular dystrophy with mental retardation and facial muscle involvement). No to Hattatsu (Brain Dev/in Japanese)(Tokyo) 1971;3:21-36.
    • (1971) No to Hattatsu (Brain Dev/in Japanese)(Tokyo) , vol.3 , pp. 21-36
    • Segawa, M.1
  • 19
    • 0015529507 scopus 로고
    • An electron microscopical study of the muscle in congenital muscular dystrophy
    • Nonaka I, Miyoshino S, Miike T, Ueno T, Usuku G. An electron microscopical study of the muscle in congenital muscular dystrophy. Kumamoto Med J 1972;25:68-82.
    • (1972) Kumamoto Med J , vol.25 , pp. 68-82
    • Nonaka, I.1    Miyoshino, S.2    Miike, T.3    Ueno, T.4    Usuku, G.5
  • 20
    • 0018868593 scopus 로고
    • Light and electron microscopic studies of congenital muscular dystrophy
    • Misugi N. Light and electron microscopic studies of congenital muscular dystrophy. Brain Dev (Tokyo) 1980;2:191-9.
    • (1980) Brain Dev (Tokyo) , vol.2 , pp. 191-199
    • Misugi, N.1
  • 21
    • 0020085750 scopus 로고
    • Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement
    • Nonaka I, Sugita H, Takada K, Kumagai K. Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement. Muscle Nerve 1982;5:102-6.
    • (1982) Muscle Nerve , vol.5 , pp. 102-106
    • Nonaka, I.1    Sugita, H.2    Takada, K.3    Kumagai, K.4
  • 22
    • 0020644090 scopus 로고
    • Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies
    • Miike T. Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies. Muscle Nerve 1983;6:545-52.
    • (1983) Muscle Nerve , vol.6 , pp. 545-552
    • Miike, T.1
  • 23
    • 0022650743 scopus 로고
    • Muscle regeneration and satellite cells in Fukuyama type congenital muscular dystrophy
    • Terasawa K. Muscle regeneration and satellite cells in Fukuyama type congenital muscular dystrophy. Muscle Nerve 1986;9:465-70.
    • (1986) Muscle Nerve , vol.9 , pp. 465-470
    • Terasawa, K.1
  • 24
    • 0025870790 scopus 로고
    • Immunocytochemical analysis of dystrophin in congenital muscular dystrophy
    • Arikawa E, Ishihara T, Nonaka I, Sugita H, Arahata K. Immunocytochemical analysis of dystrophin in congenital muscular dystrophy. J Neurol Sei 1991;105:79-87.
    • (1991) J Neurol Sei , vol.105 , pp. 79-87
    • Arikawa, E.1    Ishihara, T.2    Nonaka, I.3    Sugita, H.4    Arahata, K.5
  • 25
    • 0027360897 scopus 로고
    • Abnormal localization of laminin subunits in muscular dystrophies
    • Hayashi YK, Engvall E, Arikawa-Hirasawa E, et al. Abnormal localization of laminin subunits in muscular dystrophies. J Neurol Sei 1993; 119:53-64.
    • (1993) J Neurol Sei , vol.119 , pp. 53-64
    • Hayashi, Y.K.1    Engvall, E.2    Arikawa-Hirasawa, E.3
  • 26
    • 0027364850 scopus 로고
    • Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
    • Toda T, Segawa M, Nomura Y, et al. Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33. Nature Genet 1993;5:283-6.
    • (1993) Nature Genet , vol.5 , pp. 283-286
    • Toda, T.1    Segawa, M.2    Nomura, Y.3
  • 27
    • 0028114849 scopus 로고
    • Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: Evidence for strong linkage disequilibrium
    • Toda T, Ikegawa S, Okui K, et al. Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: Evidence for strong linkage disequilibrium. Am J Hum Genet 1994;55: 946-50.
    • (1994) Am J Hum Genet , vol.55 , pp. 946-950
    • Toda, T.1    Ikegawa, S.2    Okui, K.3
  • 28
    • 0028066764 scopus 로고
    • Human laminin M chain (merosin): Complete primary structure, chromosomal assignment. and expression of the M and a chain in human fetal tissues
    • Vuolteenaho R, Nissinen M, Sainio K, et al. Human laminin M chain (merosin): Complete primary structure, chromosomal assignment. and expression of the M and A chain in human fetal tissues. J Cell Biol 1994;124:381-94.
    • (1994) J Cell Biol , vol.124 , pp. 381-394
    • Vuolteenaho, R.1    Nissinen, M.2    Sainio, K.3
  • 29
    • 0028914964 scopus 로고
    • Three muscular dystrophies: Loss of cytoskeletonextracellular matrix linkage
    • Campbell KP. Three muscular dystrophies: Loss of cytoskeletonextracellular matrix linkage. Cell 1995;80:675-9.
    • (1995) Cell , vol.80 , pp. 675-679
    • Campbell, K.P.1
  • 30
    • 0002517253 scopus 로고
    • Supramolecular organization of basement membranes
    • Rohrbach DH, Timpl R, editors. New York: Academic Press
    • Yurchenco PD and O'Rear J. Supramolecular organization of basement membranes. In: Rohrbach DH, Timpl R, editors. Molecular and Cellular Aspects of Basement Membranes. New York: Academic Press, 1993:19-47.
    • (1993) Molecular and Cellular Aspects of Basement Membranes , pp. 19-47
    • Yurchenco, P.D.1    O'Rear, J.2
  • 31
    • 0029060893 scopus 로고
    • Workshop report: Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy
    • Dubowitz V, Fardeau M. Workshop report: Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. Neuromusc Disord 1995;5:253-8.
    • (1995) Neuromusc Disord , vol.5 , pp. 253-258
    • Dubowitz, V.1    Fardeau, M.2
  • 32
    • 0029921917 scopus 로고    scopus 로고
    • Basement membrane abnormality in merosin-negative congenital muscular dystrophy
    • Osari S, Kobayashi O, Yamashita Y, et al. Basement membrane abnormality in merosin-negative congenital muscular dystrophy. Acta Neuropathol 1996:91:332-6.
    • (1996) Acta Neuropathol , vol.91 , pp. 332-336
    • Osari, S.1    Kobayashi, O.2    Yamashita, Y.3
  • 33
    • 85008070304 scopus 로고
    • Laminin in animal models for muscular dystrophy: Defect of laminin M in skeletal and cardiac muscles and peripheral nerve of the homozygous dystrophic dy/dy mice
    • Ser B
    • Arahata K, Hayashi YK, Koga R, et al. Laminin in animal models for muscular dystrophy: Defect of laminin M in skeletal and cardiac muscles and peripheral nerve of the homozygous dystrophic dy/dy mice. Proc Jpn Acad 1993;69 Ser B:259-64.
    • (1993) Proc Jpn Acad , vol.69 , pp. 259-264
    • Arahata, K.1    Hayashi, Y.K.2    Koga, R.3
  • 35
    • 0029046994 scopus 로고
    • The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: Immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin
    • Hayashi YK, Mizuno Y, Yoshida M, et al. The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: Immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin. Neurology 1995:45:551-4.
    • (1995) Neurology , vol.45 , pp. 551-554
    • Hayashi, Y.K.1    Mizuno, Y.2    Yoshida, M.3
  • 36
    • 0027290582 scopus 로고
    • Dystrophin-associated glycoprotein and dystrophin co-localization at sarcolemma in Fukuyama congenital muscular dystrophy
    • Arahata K, Hayashi YK, Mizuno Y, Yoshida M, Ozawa E. Dystrophin-associated glycoprotein and dystrophin co-localization at sarcolemma in Fukuyama congenital muscular dystrophy. Lancet 1993:342:623-4.
    • (1993) Lancet , vol.342 , pp. 623-624
    • Arahata, K.1    Hayashi, Y.K.2    Mizuno, Y.3    Yoshida, M.4    Ozawa, E.5
  • 37
    • 0023472169 scopus 로고
    • Muscle fiber growth and necrosis in dystrophic muscles: A comparative study between dy and mdx
    • Woo M, Tanabe Y, Ishii H, et al. Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx. J Neurol Sei 1987;82:111-22.
    • (1987) J Neurol Sei , vol.82 , pp. 111-122
    • Woo, M.1    Tanabe, Y.2    Ishii, H.3
  • 38
    • 0015724523 scopus 로고
    • An ultrastructural observation of satellite cells in the biopsied muscle of congenital muscular dystrophy
    • Nonaka I, Miike T, Ueno T, Miyoshino S. An ultrastructural observation of satellite cells in the biopsied muscle of congenital muscular dystrophy. No to Hattatsu (Brain Dev/in Japanese)(Tokyo) 1973:5: 80-9.
    • (1973) No to Hattatsu (Brain Dev/in Japanese)(Tokyo) , vol.5 , pp. 80-89
    • Nonaka, I.1    Miike, T.2    Ueno, T.3    Miyoshino, S.4
  • 40
    • 0024535958 scopus 로고
    • A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction
    • Hunter DD, Shah V, Merlie JP, Sanes JR. A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction. Nature 1989;338:229-34.
    • (1989) Nature , vol.338 , pp. 229-234
    • Hunter, D.D.1    Shah, V.2    Merlie, J.P.3    Sanes, J.R.4
  • 42
    • 0028098737 scopus 로고
    • Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin
    • Higuchi I. Yamada H, Fukunaga H, et al. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. J Clin Invest 1994;94:601-6.
    • (1994) J Clin Invest , vol.94 , pp. 601-606
    • Higuchi, I.1    Yamada, H.2    Fukunaga, H.3
  • 43
    • 0028972907 scopus 로고
    • Abnormal expression of heparan sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency
    • Higuchi I, Fukunaga H, Matsumura K, et al. Abnormal expression of heparan sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency. Neuromusc Disord 1995;5:467-74.
    • (1995) Neuromusc Disord , vol.5 , pp. 467-474
    • Higuchi, I.1    Fukunaga, H.2    Matsumura, K.3
  • 44
    • 0029396750 scopus 로고
    • Laminin 32 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy)
    • Wewer UM, Durkin ME, Zhang X, et al. Laminin (32 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy). Neurology 1995;45:2099-101.
    • (1995) Neurology , vol.45 , pp. 2099-2101
    • Wewer, U.M.1    Durkin, M.E.2    Zhang, X.3
  • 45
    • 0028334735 scopus 로고
    • Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse
    • Xu H, Christmas P, Wu X-R, et al. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc Natl Acad Sei USA 1994;91:5572-6.
    • (1994) Proc Natl Acad Sei USA , vol.91 , pp. 5572-5576
    • Xu, H.1    Christmas, P.2    Wu, X.-R.3
  • 46
    • 0016718398 scopus 로고
    • Genetically determined defect of Schwann cell basement membrane in dystrophic mouse
    • Madrid RE, Jaros E, Cullen MJ, Bradley WG. Genetically determined defect of Schwann cell basement membrane in dystrophic mouse. Nature 1975;257:319-21.
    • (1975) Nature , vol.257 , pp. 319-321
    • Madrid, R.E.1    Jaros, E.2    Cullen, M.J.3    Bradley, W.G.4


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