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Volumn 18, Issue 4, 1998, Pages 362-365

Microlissencephaly

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARAB; ARTICLE; CASE REPORT; CORPUS CALLOSUM AGENESIS; HUMAN; INFANT; MALE; MICROCEPHALY; PACHYGYRIA; PRIORITY JOURNAL;

EID: 0031943631     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(97)00213-0     Document Type: Article
Times cited : (28)

References (9)
  • 1
    • 0029000061 scopus 로고
    • Lissencephaly and other malformations of cortical development: 1995 update
    • Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics 1995;26: 132-47.
    • (1995) Neuropediatrics , vol.26 , pp. 132-147
    • Dobyns, W.B.1    Truwit, C.L.2
  • 2
    • 0020075263 scopus 로고
    • Familial lissencephaly with extreme neopallial hypoplasia
    • Barth PG, Mullaart R, Stam FC, Slooff JL. Familial lissencephaly with extreme neopallial hypoplasia. Brain Dev 1982;4:145-51.
    • (1982) Brain Dev , vol.4 , pp. 145-151
    • Barth, P.G.1    Mullaart, R.2    Stam, F.C.3    Slooff, J.L.4
  • 3
    • 10544240253 scopus 로고
    • Cerebrocerebellar lissencephaly, congenital heart defects and other congenital anomalies in male sibs: A new syndrome
    • Vancouver, BC, Canada
    • McComb R, Schaefer B, Olney A, Hattie B. Cerebrocerebellar lissencephaly, congenital heart defects and other congenital anomalies in male sibs: a new syndrome. Proceedings of the Birth Defects Conference, Vancouver, BC, Canada, 1991.
    • (1991) Proceedings of the Birth Defects Conference
    • McComb, R.1    Schaefer, B.2    Olney, A.3    Hattie, B.4
  • 4
    • 0029804898 scopus 로고    scopus 로고
    • Lissencephaly with extreme cerebral and cerebellar hypoplasia. a magnetic resonance imaging study
    • Kroon AA, Amit BJ, Barth PG, Hennekam RCM. Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study. Neuropediatrics 1996 27:273-6.
    • (1996) Neuropediatrics , vol.27 , pp. 273-276
    • Kroon, A.A.1    Amit, B.J.2    Barth, P.G.3    Hennekam, R.C.M.4
  • 6
    • 0022550695 scopus 로고
    • Arthrogryposis multiplex congenita: Spectrum of pathologic changes
    • Banker BQ, Arthrogryposis multiplex congenita: Spectrum of pathologic changes. Hum Pathol 1986;17:656-72.
    • (1986) Hum Pathol , vol.17 , pp. 656-672
    • Banker, B.Q.1
  • 8
    • 0024395161 scopus 로고
    • Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia
    • Dobyns WB. Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia. Neurology 1989;39:817-20.
    • (1989) Neurology , vol.39 , pp. 817-820
    • Dobyns, W.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.