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Volumn 21, Issue 4, 1997, Pages 355-360

Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy

Author keywords

Basement membrane; Central nervous system; Fukuyama congenital muscular dystrophy; Ultrastructure

Indexed keywords

ADULT; ARTICLE; BASEMENT MEMBRANE; CASE REPORT; CENTRAL NERVOUS SYSTEM; CONGENITAL DISORDER; CONTROLLED STUDY; FETUS; HUMAN; HUMAN TISSUE; MALE; MUSCULAR DYSTROPHY; PRIORITY JOURNAL; ULTRASTRUCTURE;

EID: 0030944752     PISSN: 01913123     EISSN: None     Source Type: Journal    
DOI: 10.3109/01913129709021933     Document Type: Article
Times cited : (22)

References (21)
  • 1
    • 0019471880 scopus 로고
    • Congenital progressive muscular dystrophy of the Fukuyama type. Clinical, genetic, and pathological considerations
    • Fukuyama Y, Osawa M, Suzuki H. Congenital progressive muscular dystrophy of the Fukuyama type. Clinical, genetic, and pathological considerations. Brain Dev. 1981;3: 1-29.
    • (1981) Brain Dev. , vol.3 , pp. 1-29
    • Fukuyama, Y.1    Osawa, M.2    Suzuki, H.3
  • 2
    • 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;33:513-516.
    • (1976) Arch Neurol. , vol.33 , pp. 513-516
    • Kamoshita, S.1    Konishi, Y.2    Segawa, M.3    Fukuyama, Y.4
  • 4
    • 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
  • 5
    • 0023937158 scopus 로고
    • Fukuyama congenital muscular dystrophy as a unique disorder of neuronal migration: A neuropathological review and hypothesis
    • Takada K. Fukuyama congenital muscular dystrophy as a unique disorder of neuronal migration: a neuropathological review and hypothesis. Yonago Acta Med. 1988;31:1-16.
    • (1988) Yonago Acta Med. , vol.31 , pp. 1-16
    • Takada, K.1
  • 6
    • 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;55:946-950.
    • (1994) Am J Hum Genet. , vol.55 , pp. 946-950
    • Toda, T.1    Ikegawa, S.2    Okui, K.3
  • 7
    • 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. Nat Genet. 1993;5:283-286.
    • (1993) Nat Genet. , vol.5 , pp. 283-286
    • Toda, T.1    Segawa, M.2    Nomura, Y.3
  • 8
    • 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;74:300-306.
    • (1987) Acta Neuropathol. , vol.74 , pp. 300-306
    • Takada, K.1    Nakamura, H.2    Suzumori, K.3    Ishikawa, T.4    Sugiyama, N.5
  • 9
    • 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;91:313-321.
    • (1996) Acta Neuropathol. , vol.91 , pp. 313-321
    • Nakano, I.1    Funahashi, M.2    Takada, K.3    Toda, T.4
  • 10
    • 0029759153 scopus 로고    scopus 로고
    • Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20-week fetus
    • Yamamoto T, Komori T, Shibata N, et al. Fukuyama congenital muscular dystrophy: cortical dysplasia of the cerebrum in a 20-week fetus. Neuropathology. 1996;16:184-189.
    • (1996) Neuropathology , vol.16 , pp. 184-189
    • Yamamoto, T.1    Komori, T.2    Shibata, N.3
  • 11
    • 0031051605 scopus 로고    scopus 로고
    • Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
    • Yamamoto T, Toyoda C, Kobayashi M, Kondo E, Saito K, Osawa M. Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy. Brain Dev. 1997;19:35-42.
    • (1997) Brain Dev. , vol.19 , pp. 35-42
    • Yamamoto, T.1    Toyoda, C.2    Kobayashi, M.3    Kondo, E.4    Saito, K.5    Osawa, M.6
  • 13
    • 0022510331 scopus 로고
    • Glial fibrillary acidic protein in radial glia of early human fetal cerebrum: A light and electron microscopic immunoperoxidase study
    • Choi BH. Glial fibrillary acidic protein in radial glia of early human fetal cerebrum: a light and electron microscopic immunoperoxidase study. J Neuropathol Exp Neurol. 1986;45:408-418.
    • (1986) J Neuropathol Exp Neurol. , vol.45 , pp. 408-418
    • Choi, B.H.1
  • 14
    • 0030456594 scopus 로고    scopus 로고
    • Prenatal diagnosis in Fukuyama type congenital muscular dystrophy by polymorphism analysis
    • Kondo E, Saito K, Toda T, Osawa M, Fukuyama Y. Prenatal diagnosis in Fukuyama type congenital muscular dystrophy by polymorphism analysis. Am J Med Genet. 1996;66:169-174.
    • (1996) Am J Med Genet. , vol.66 , pp. 169-174
    • Kondo, E.1    Saito, K.2    Toda, T.3    Osawa, M.4    Fukuyama, Y.5
  • 15
    • 0029875997 scopus 로고    scopus 로고
    • Dystrophin-associated proteins and the muscular dystrophies: A glossary
    • Brown RH Jr. Dystrophin-associated proteins and the muscular dystrophies: a glossary. Brain Pathol. 1996;6:19-24.
    • (1996) Brain Pathol. , vol.6 , pp. 19-24
    • Brown Jr., R.H.1
  • 16
    • 0028047235 scopus 로고
    • Dystrophin-glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophies
    • Matsumura K, Campbell KP. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Muscle Nerve. 1994;17:2-15.
    • (1994) Muscle Nerve. , vol.17 , pp. 2-15
    • Matsumura, K.1    Campbell, K.P.2
  • 17
    • 0027360897 scopus 로고
    • Abnormal localization of laminin subunits in muscular dystrophies
    • Hayashi YK, Engvall E, Arisawa-Hirasawa E, et al. Abnormal localization of laminin subunits in muscular dystrophies. J Neurol Sci. 1993;119:53-64.
    • (1993) J Neurol Sci. , vol.119 , pp. 53-64
    • Hayashi, Y.K.1    Engvall, E.2    Arisawa-Hirasawa, E.3
  • 18
    • 0027458810 scopus 로고
    • Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy
    • Matusmura K, Nonaka I, Campbell KP. Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy. Lancet. 1993;341:521-522.
    • (1993) Lancet , vol.341 , pp. 521-522
    • Matusmura, K.1    Nonaka, I.2    Campbell, K.P.3
  • 20
    • 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;91:332-336.
    • (1996) Acta Neuropathol. , vol.91 , pp. 332-336
    • Osari, S.1    Kobayashi, O.2    Yamashita, Y.3
  • 21
    • 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
    • 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(B):259-264.
    • (1993) Proc Jpn Acad. , vol.69 , Issue.B , pp. 259-264
    • Arahata, K.1    Hayashi, Y.K.2    Koga, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.