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Volumn 36, Issue 6, 2007, Pages 418-420

Bilateral Perisylvian Polymicrogyria and Chromosome 1 Anomaly

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 1; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CYTOGENETICS; CYTOMEGALOVIRUS; DISEASE ASSOCIATION; EPILEPSY; FEMALE; FETUS MALFORMATION; GROWTH RETARDATION; HUMAN; HYPOTHYROIDISM; MACROCEPHALY; MICROGYRIA; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SUPRASYLVIAN GYRUS;

EID: 34249895003     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2007.01.015     Document Type: Article
Times cited : (14)

References (10)
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    • Fan Y.S., Jung J., and Hamilton B. Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. Am J Med Genet 86 (1999) 118-123
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  • 2
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    • Maternal pericentric inversion in the origin of an abnormal child due to a recombinant chromosome 1: implications for genetic counseling
    • Pinto M.R., Aguiar J., and Mota C.R. Maternal pericentric inversion in the origin of an abnormal child due to a recombinant chromosome 1: implications for genetic counseling. Genet Counsel 11 (2000) 179-180
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  • 3
    • 0034891040 scopus 로고    scopus 로고
    • Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disorders
    • Blinder G., Corat-Simon J., and Hershkovitz E. Micropituitarism and cortical dysplasia: an unknown association of two uncommon CNS disorders. Eur Radiol 11 (2001) 1070-1072
    • (2001) Eur Radiol , vol.11 , pp. 1070-1072
    • Blinder, G.1    Corat-Simon, J.2    Hershkovitz, E.3
  • 4
    • 18844370078 scopus 로고    scopus 로고
    • Genetics of the polymicrogyria syndromes
    • Jansen A., and Andermann E. Genetics of the polymicrogyria syndromes. J Med Genet 42 (2005) 369-378
    • (2005) J Med Genet , vol.42 , pp. 369-378
    • Jansen, A.1    Andermann, E.2
  • 5
    • 0032716092 scopus 로고    scopus 로고
    • Syndromes of bilateral symmetrical polymicrogyria
    • Barkovich A.J., Hevner R., and Guerrini R. Syndromes of bilateral symmetrical polymicrogyria. Am J Neuroradiol 20 (1999) 1814-1821
    • (1999) Am J Neuroradiol , vol.20 , pp. 1814-1821
    • Barkovich, A.J.1    Hevner, R.2    Guerrini, R.3
  • 6
    • 32144433872 scopus 로고    scopus 로고
    • A developmental and genetic classification for malformations of cortical development
    • Barkovich A.J., Kuzniecky R.I., Jackson G.D., Guerrini R., and Dobyns W.B. A developmental and genetic classification for malformations of cortical development. Neurology 65 (2005) 1873-1887
    • (2005) Neurology , vol.65 , pp. 1873-1887
    • Barkovich, A.J.1    Kuzniecky, R.I.2    Jackson, G.D.3    Guerrini, R.4    Dobyns, W.B.5
  • 7
    • 34249904082 scopus 로고    scopus 로고
    • Lopate G. Congenital muscular dystrophy [Internet]. Available at: http://www.emedicine.com. Accessed January 2, 2007.
  • 9
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    • Pachygyria and polymicrogyria in 22q11 deletion syndrome
    • [Erratum in: Am J Med Genet A. 2005;136:224]
    • Ehara H., Maegaki Y., and Takeshita K. Pachygyria and polymicrogyria in 22q11 deletion syndrome. Am J Med Genet 117 (2003) 80-82 [Erratum in: Am J Med Genet A. 2005;136:224]
    • (2003) Am J Med Genet , vol.117 , pp. 80-82
    • Ehara, H.1    Maegaki, Y.2    Takeshita, K.3
  • 10
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    • A study of 220 patients with polymicrogyria delineates distinct phenotypes and reveals genetic loci on chromosomes 1p, 2p, 6q, 21q and 22q
    • [Abstract]
    • Leventer R.J., Lese C.M., Cardoso C., et al. A study of 220 patients with polymicrogyria delineates distinct phenotypes and reveals genetic loci on chromosomes 1p, 2p, 6q, 21q and 22q. [Abstract]. Am J Hum Genet 69 Suppl (2001) 177
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.