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Volumn 50, Issue 5, 1998, Pages 1466-1469

Agyria-pachygyria and agenesis of the corpus callosum: Autosomal recessive inheritance with neonatal death

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARTICLE; ASPHYXIA; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CORPUS CALLOSUM AGENESIS; CYTOGENETICS; FEMALE; HUMAN; INTRACTABLE EPILEPSY; INTRAUTERINE INFECTION; MALE; METABOLIC DISORDER; MICROCEPHALY; NEWBORN; NEWBORN MORTALITY; PACHYGYRIA; PRIORITY JOURNAL;

EID: 0031816178     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.5.1466     Document Type: Article
Times cited : (9)

References (10)
  • 2
    • 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;26:132-147.
    • (1995) Neuropediatrics , vol.26 , pp. 132-147
    • Dobyns, W.B.1    Truwit, C.L.2
  • 5
    • 0029804898 scopus 로고    scopus 로고
    • Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study
    • Kroon AA, Smit BJ, Barth PG, Hennekam RCM. Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study. Neuropediatrics 1996;27:273-276.
    • (1996) Neuropediatrics , vol.27 , pp. 273-276
    • Kroon, A.A.1    Smit, B.J.2    Barth, P.G.3    Hennekam, R.C.M.4
  • 6
    • 0028129844 scopus 로고
    • Metabolic disorders of embryogenesis
    • Brown GK. Metabolic disorders of embryogenesis. J Inherit Metab Dis 1994;17:448-458.
    • (1994) J Inherit Metab Dis , vol.17 , pp. 448-458
    • Brown, G.K.1
  • 7
    • 0029562888 scopus 로고
    • Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1α subunit mutations in females
    • Otero LJ, Brown GK, Silver K, Arnold DL, Matthews PM. Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1α subunit mutations in females. Pediatr Neurol 1995;13:327-332.
    • (1995) Pediatr Neurol , vol.13 , pp. 327-332
    • Otero, L.J.1    Brown, G.K.2    Silver, K.3    Arnold, D.L.4    Matthews, P.M.5
  • 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;39:817-820.
    • (1989) Neurology , vol.39 , pp. 817-820
    • Dobyns, W.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.