메뉴 건너뛰기




Volumn 146, Issue 22, 2008, Pages 2871-2878

Neuroimaging aspects of aicardi syndrome

Author keywords

Aicardi syndrome; Cerebellum; Corpus callosum; Heterotopias; Polymicrogyria; Tectum

Indexed keywords

AICARDI GOUTIERES SYNDROME; ARTICLE; BRAIN CYST; CEREBELLUM; CHILD; CLINICAL ARTICLE; CORPUS CALLOSUM AGENESIS; FEMALE; GENE MUTATION; HEMISPHERE; HETEROTOPIA; HUMAN; MALE; MICROGYRIA; NEUROIMAGING; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; THALAMUS;

EID: 56049094136     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32537     Document Type: Article
Times cited : (65)

References (32)
  • 1
  • 3
    • 0019299076 scopus 로고
    • Aicardi syndrome in a male infant. Editorial correspondence
    • Aicardi J. 1980. Aicardi syndrome in a male infant. Editorial correspondence. J Pediatr 97:1040-1041.
    • (1980) J Pediatr , vol.97 , pp. 1040-1041
    • Aicardi, J.1
  • 4
    • 14644402393 scopus 로고    scopus 로고
    • Aicardi syndrome
    • Aicardi J. 2005. Aicardi syndrome. Brain Dev 27:164-171.
    • (2005) Brain Dev , vol.27 , pp. 164-171
    • Aicardi, J.1
  • 6
    • 0035936638 scopus 로고    scopus 로고
    • Callosal agenesis with cyst:Abetter understanding andnewclassification
    • Barkovich AJ, Simon EM, Walsh CA. 2001. Callosal agenesis with cyst:Abetter understanding andnewclassification. Neurology 56:220-227.
    • (2001) Neurology , vol.56 , pp. 220-227
    • Barkovich, A.J.1    Simon, E.M.2    Walsh, C.A.3
  • 7
    • 32144433872 scopus 로고    scopus 로고
    • A developmental and genetic classification for malformations of cortical development
    • Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. 2005. A developmental and genetic classification for malformations of cortical development. Neurology 65:1873-1887.
    • (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
  • 8
    • 0029150742 scopus 로고
    • MR of the cerebral operculum: Topographic identification and measurement of interopercular distances in healthy infants and children
    • Chen CY, Zimmerman RA, Faro S, Parrish B, Wang Z, Bilaniuk LT, Chou TY. 1995. MR of the cerebral operculum: Topographic identification and measurement of interopercular distances in healthy infants and children. Am J Neuroradiol 16:1677-1687.
    • (1995) Am J Neuroradiol , vol.16 , pp. 1677-1687
    • Chen, C.Y.1    Zimmerman, R.A.2    Faro, S.3    Parrish, B.4    Wang, Z.5    Bilaniuk, L.T.6    Chou, T.Y.7
  • 12
    • 34249848178 scopus 로고
    • Aicardi syndrome in a male infant. Editorial correspondence
    • Hunter AGW. 1980. Aicardi syndrome in a male infant. Editorial correspondence. J Pediatr 97:1041-1042.
    • (1980) J Pediatr , vol.97 , pp. 1041-1042
    • Hunter, A.G.W.1
  • 13
    • 33749649813 scopus 로고    scopus 로고
    • Aicardi syndrome: Chorioretinal lacunae without corpus callosum agenesis
    • Iturralde D, Meyerle CB, Yannuzzi LA. 2006. Aicardi syndrome: Chorioretinal lacunae without corpus callosum agenesis. Retina 26:977-978.
    • (2006) Retina , vol.26 , pp. 977-978
    • Iturralde, D.1    Meyerle, C.B.2    Yannuzzi, L.A.3
  • 14
    • 33751016367 scopus 로고    scopus 로고
    • Cerebral developmental disorders
    • Lian G, Sheen V. 2006. Cerebral developmental disorders. Curr Opin Pediatr 18:614-620.
    • (2006) Curr Opin Pediatr , vol.18 , pp. 614-620
    • Lian, G.1    Sheen, V.2
  • 18
    • 29144470390 scopus 로고    scopus 로고
    • Oculocerebro-cutaneous syndrome: The brain malformation defines a core phenotype
    • Moog U, Jones MC, Bird LM, Dobyns WB. 2005. Oculocerebro-cutaneous syndrome: The brain malformation defines a core phenotype. J Med Genet 42:913-921.
    • (2005) J Med Genet , vol.42 , pp. 913-921
    • Moog, U.1    Jones, M.C.2    Bird, L.M.3    Dobyns, W.B.4
  • 20
    • 45849138222 scopus 로고    scopus 로고
    • Aicardi syndrome in monozygotic twins
    • Pons ME, Garcia CA. 2008. Aicardi syndrome in monozygotic twins. Ophthalmic Genet 29:87-88.
    • (2008) Ophthalmic Genet , vol.29 , pp. 87-88
    • Pons, M.E.1    Garcia, C.A.2
  • 22
    • 0029882297 scopus 로고    scopus 로고
    • Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS)
    • Schaefer L, Ballabio A, Zoghbi HY. 1996. Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS). Genomics 34:166-172.
    • (1996) Genomics , vol.34 , pp. 166-172
    • Schaefer, L.1    Ballabio, A.2    Zoghbi, H.Y.3
  • 23
    • 0031452913 scopus 로고    scopus 로고
    • Cloning and characterization of a novel rho-type GTPase-activating protein gene (ARHGAP6) from the critical region for microphthalmia with linear skin defects
    • Schaefer L, Prakash S, Zoghbi HY. 1997. Cloning and characterization of a novel rho-type GTPase-activating protein gene (ARHGAP6) from the critical region for microphthalmia with linear skin defects. Genomics 46:268-277.
    • (1997) Genomics , vol.46 , pp. 268-277
    • Schaefer, L.1    Prakash, S.2    Zoghbi, H.Y.3
  • 24
    • 0029808121 scopus 로고    scopus 로고
    • Magnetic resonance imaging of the brain in Aicardi's syndrome. Report of 20 patients
    • Smith CD, Ryan SJ, Hoover SL, Baumann RJ. 1996. Magnetic resonance imaging of the brain in Aicardi's syndrome. Report of 20 patients. J Neuroimaging 6:214-221.
    • (1996) J Neuroimaging , vol.6 , pp. 214-221
    • Smith, C.D.1    Ryan, S.J.2    Hoover, S.L.3    Baumann, R.J.4
  • 26
    • 0344099463 scopus 로고    scopus 로고
    • Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: Are they related X-linked dominant male-lethal disorders?
    • Van den Veyver IB. 2002. Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: Are they related X-linked dominant male-lethal disorders? Cytogenet Genome Res 99:289-296.
    • (2002) Cytogenet Genome Res , vol.99 , pp. 289-296
    • Van den Veyver, I.B.1
  • 27
    • 0032527775 scopus 로고    scopus 로고
    • Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22
    • Van den Veyver IB, Cormier TA, Jurecic V, Baldini A, Zoghbi HY. 1998. Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22. Genomics 51:251-261.
    • (1998) Genomics , vol.51 , pp. 251-261
    • Van den Veyver, I.B.1    Cormier, T.A.2    Jurecic, V.3    Baldini, A.4    Zoghbi, H.Y.5
  • 30
    • 0020518307 scopus 로고
    • X-linked dominant inherited diseases with lethality in hemizygous males
    • Wettke-Schafer R, Kantner G. 1983. X-linked dominant inherited diseases with lethality in hemizygous males. Hum Genet 64:1-23.
    • (1983) Hum Genet , vol.64 , pp. 1-23
    • Wettke-Schafer, R.1    Kantner, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.