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Volumn 46, Issue 4, 1999, Pages 660-663

Diffuse pachygyria with cerebellar hypoplasia: A milder form of microlissencephaly or a new genetic syndrome?

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARTICLE; ATAXIA; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CEREBELLUM HYPOPLASIA; COMPUTER ASSISTED TOMOGRAPHY; DISEASE ASSOCIATION; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MUSCLE HYPOTONIA; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PHENOTYPE; PRIORITY JOURNAL;

EID: 0032831013     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(199910)46:4<660::AID-ANA17>3.0.CO;2-Q     Document Type: Article
Times cited : (22)

References (13)
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    • (1998) Hum Mol Genet , vol.7 , pp. 2029-2037
    • Pilz, D.T.1    Matsumoto, N.2    Minnerath, S.3
  • 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;4:145-151
    • (1982) Brain Dev , vol.4 , pp. 145-151
    • Barth, P.G.1    Mullaart, R.2    Stam, F.C.3    Slooff, J.L.4
  • 3
    • 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
  • 4
    • 0029804898 scopus 로고    scopus 로고
    • Lissencephaly with extreme cerebral and cerebellar hypoplasia: A magnetic resonance imaging study
    • Kroon AA, Smit BJ, Barth PG, Hennekam RC. 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.4
  • 5
    • 0030959134 scopus 로고    scopus 로고
    • Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: A new syndrome?
    • Farah S, Sabry MA, Khuraibet A, et al. Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome? Clin Genet 1997;51: 326-330
    • (1997) Clin Genet , vol.51 , pp. 326-330
    • Farah, S.1    Sabry, M.A.2    Khuraibet, A.3
  • 6
    • 0022118788 scopus 로고
    • Further comments on the lissencephaly syndromes
    • Dobyns WB, Gilbert EF, Opitz JM. Further comments on the lissencephaly syndromes. Am J Med Genet 1985;22:197-211
    • (1985) Am J Med Genet , vol.22 , pp. 197-211
    • Dobyns, W.B.1    Gilbert, E.F.2    Opitz, J.M.3
  • 8
    • 0028859547 scopus 로고
    • Two cases of possible cerebrocerebellar lissencephaly variant of type I
    • Sugama S, Kusano K. Two cases of possible cerebrocerebellar lissencephaly variant of type I [Japanese]. No Hattatsu 1995; 27:502-504
    • (1995) No Hattatsu , vol.27 , pp. 502-504
    • Sugama, S.1    Kusano, K.2
  • 9
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    • Cerebellar agenesia associated with microcephaly and agyria: Report of a case in a newborn and review of the literature
    • Pittella JE, Nogueira AM. Cerebellar agenesia associated with microcephaly and agyria: report of a case in a newborn and review of the literature [Portugese]. Arq Neuro-Psiquiat 1988; 46:385-392
    • (1988) Arq Neuro-Psiquiat , vol.46 , pp. 385-392
    • Pittella, J.E.1    Nogueira, A.M.2
  • 10
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    • A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema
    • Hourihane JO, Bennett CP, Chaudhuri R, et al. A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema. Neuropediatrics 1993;24:43-46
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.