메뉴 건너뛰기




Volumn 19, Issue 1, 1997, Pages 35-42

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

Author keywords

Fetus; Fukuyama congenital muscular dystrophy; Immunohistochemistry; Pial glial barrier

Indexed keywords

PROTEIN S 100;

EID: 0031051605     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(96)00056-3     Document Type: Article
Times cited : (49)

References (21)
  • 1
    • 0002618558 scopus 로고
    • A peculiar form of congenital progressive muscular dystrophy. Report of fifteen cases
    • Fukuyama Y, Kawazura M, Haruna H. A peculiar form of congenital progressive muscular dystrophy. Report of fifteen cases. Pediatr. Univ. Tokyo (Tokyo) 1960; 4: 5-8.
    • (1960) Pediatr. Univ. Tokyo (Tokyo) , vol.4 , pp. 5-8
    • Fukuyama, Y.1    Kawazura, M.2    Haruna, H.3
  • 2
    • 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. (Tokyo) 1981; 3: 1-29.
    • (1981) Brain Dev. (Tokyo) , vol.3 , pp. 1-29
    • Fukuyama, Y.1    Osawa, M.2    Suzuki, H.3
  • 3
    • 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. Neural. 1976; 33: 513-516.
    • (1976) Arch. Neural. , vol.33 , pp. 513-516
    • Kamoshita, S.1    Konishi, Y.2    Segawa, M.3    Fukuyama, Y.4
  • 4
    • 0342869744 scopus 로고
    • Fukuyama type congenital progressive muscular dystrophy (FCMD). Special comment on the relationship between the case reported by Nakayama et al and FCMD
    • Osawa M, Suzuki N, Arai Y, et al. Fukuyama type congenital progressive muscular dystrophy (FCMD). Special comment on the relationship between the case reported by Nakayama et al and FCMD. Neuropathology (Tokyo) 1993; 13: 259-268.
    • (1993) Neuropathology (Tokyo) , vol.13 , pp. 259-268
    • Osawa, M.1    Suzuki, N.2    Arai, Y.3
  • 5
    • 0021136592 scopus 로고
    • Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type)
    • Takada K, Nakamura H, Tanaka. 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    Tanaka3
  • 6
    • 0042923468 scopus 로고
    • Cerebral dysgenesis
    • New York: Oxford University Press
    • Sarnat HB. Cerebral dysgenesis. Embryonal and Clinical Expression. New York: Oxford University Press, 1992: 245-274.
    • (1992) Embryonal and Clinical Expression , pp. 245-274
    • Sarnat, H.B.1
  • 7
    • 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. (Yonago) 1988; 31: 1-16.
    • (1988) Yonago Acta Med. (Yonago) , vol.31 , pp. 1-16
    • Takada, K.1
  • 8
    • 0023231444 scopus 로고
    • Cortical dysplasia in a 23-week fetus with Fukuyama congenital uscular dystrophy (FCMD)
    • Takada K, Nakamura H, Suzumori K, Ishikawa T, Sugiyama N. Cortical dysplasia in a 23-week fetus with Fukuyama congenital uscular 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 branches of the glia limitans the primary cause of the micropolygyria of Fukuyamatype congenital muscular dystrophy (FCMD)? - Pathological study of the cerebral cortex of a FCMD fetus
    • Nakano I, Funahashi M, Takada K, et al. Are branches of the glia limitans the primary cause of the micropolygyria of Fukuyamatype congenital muscular dystrophy (FCMD)? - Pathological study of the cerebral cortex of a 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
  • 10
    • 0343304764 scopus 로고    scopus 로고
    • Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20-week fetus
    • in press
    • Yamamoto T, Komori T, Shibata N et al. Fukuyama congenital muscular dystrophy: cortical dysplasia of the cerebrum in a 20-week fetus. Neuropathology (Tokyo), in press.
    • Neuropathology (Tokyo)
    • Yamamoto, T.1    Komori, T.2    Shibata, N.3
  • 11
    • 0030456594 scopus 로고    scopus 로고
    • Prenatal diagnosis in Fukuyama type congenital muscular dystrophy by polymorphisms analysis
    • in press
    • Kondo E, Saito K, Toda T, Osawa M, Fukuyama Y. Prenatal diagnosis in Fukuyama type congenital muscular dystrophy by polymorphisms analysis. Am. J. Med. Genet., in press.
    • Am. J. Med. Genet.
    • Kondo, E.1    Saito, K.2    Toda, T.3    Osawa, M.4    Fukuyama, Y.5
  • 12
    • 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
  • 13
    • 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
  • 15
    • 0013828515 scopus 로고
    • Marginal glioneural heterotopias of the central nervous system
    • Brun A. Marginal glioneural heterotopias of the central nervous system. Acta Pathol. Microbiol. Scand. 1965; 65: 221-233.
    • (1965) Acta Pathol. Microbiol. Scand. , vol.65 , pp. 221-233
    • Brun, A.1
  • 16
    • 0015846291 scopus 로고
    • Neuronal migration, with special reference to developing human brain: A review
    • Sidman RL, Rakic P. Neuronal migration, with special reference to developing human brain: A review. Brain Res. 1973; 62: 1-35.
    • (1973) Brain Res. , vol.62 , pp. 1-35
    • Sidman, R.L.1    Rakic, P.2
  • 17
    • 0022256291 scopus 로고
    • Meningeal cells are involved in foliation, lamination, and neurogenesis of the cerebellum: Evidence from 6-hydroxydopamine-induced destruction of meningeal cells
    • Pehlemann FW, Sievers J, Berry M. Meningeal cells are involved in foliation, lamination, and neurogenesis of the cerebellum: evidence from 6-hydroxydopamine-induced destruction of meningeal cells. Dev. Biol. 1985; 110: 136-146.
    • (1985) Dev. Biol. , vol.110 , pp. 136-146
    • Pehlemann, F.W.1    Sievers, J.2    Berry, M.3
  • 19
    • 0022611338 scopus 로고
    • Destruction of meningeal cells over the new born hamster cerebellum with 6-hydroxydopamine prevents foliation and lamination in the rostral cerebellum
    • Von Knebel Doeberitz C, Sievers J, Sadler M, Pehlemann FW, Berry M, Halliwell P. Destruction of meningeal cells over the new born hamster cerebellum with 6-hydroxydopamine prevents foliation and lamination in the rostral cerebellum. Neuroscience 1986; 17: 409-426.
    • (1986) Neuroscience , vol.17 , pp. 409-426
    • Von Knebel Doeberitz, C.1    Sievers, J.2    Sadler, M.3    Pehlemann, F.W.4    Berry, M.5    Halliwell, P.6
  • 20
    • 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
  • 21
    • 0027360897 scopus 로고
    • Abnormal localization of laminin subunits in muscular dystrophies
    • Hayashi YK, Engvall E, Arahata-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    Arahata-Hirasawa, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.