References
- Leventer RJ, Guerrini R, Dobyns WB. Malformations of cortical development and epilepsy. Dialogues Clin Neurosci 2008;10:47–62.
- Serdal G, Dilek Y, Güzide T, Işıl, Emel EB, Meral T. Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I). Turk J Pediatr 2007;49:120–130.
- Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R. Classification system for malformations of cortical development, update 2001. Neurology 2001;57:2168–2178.
- Montenegro MA, Gerreiro MM, Lopes-Cendes I, Guerreiro CA, Cendes F. Interrelationship of genetics and prenatal injury in the genesis of malformations of cortical development. Arch Neurol 2002;59:1147–1153.
- Barkovich AJ, Raybaud C. Pediatric Neuroimaging. 5th ed. Philadelphia: Wolters Kluwer. 2012.
- Dobins B, Truwit C. Lissencephaly and other manifestations of cortical development, 1995 update. Neuropediatrics 1995;26:132–147.
- Barkovich AJ, Koch TK, Carrol CL. The spectrum of lissencephaly: report of ten patients analyzed by magnetic resonance imaging. Ann Neurol 1991;30:139–114.
- Barkovich AJ. Morphologic characteristics of subcortical heterotopia: MR imaging study. AJNR Am J Neuroradiol 2000;21:290–295.
- Barkovich AJ, Guerrini R, Battaglia G, Kalifa G, N’Guyen T, Parmeggiani A, Santucci M. Band heterotopia: correlation of outcome whit magnetic resonance imaging parameters. Ann Neurol 1994;36:609–617.
- Guerrini R, Carozzo R. Epilepsy and genetic malformations of the cerebral cortex. Am J Med Genet 2001;106:160–173.
- Janj MA, Woo HI, Kim JW, Lee J, Ki CS. Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing. Pediatr Neurol 2013;48:411–414.
- Leger PL, Souville I. The location of DCX mutations predicts malformation severity in x-linked lissencephaly. Neurogenetics 2008;9:277–285.
- Guerrini R, Filippi T. Neuronal migrations disorders, genetics and epileptogenesis. J Child Neurol 2005;20:287–299.
- Guerrini R, Filippi T. Neuronal migrations disorders, genetics and epileptogenesis. J Child Neurol 2005;20:287–299.
- Sicca F, kelemen A, Genton P, et al. Mosaic mutations of the LIS1 gene cause subcortical band heterotopia. Neurology 2003;61:1042–1046.
- Cardoso C, Leventer RJ, Matsumoto N, Kuc JA, Ramocki MB, Mewborn SK, Dudlicek LL, May LF, Mills PL, Das S, Pilz DT, Dobyns WB, Ledbetter DH. The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene. Hum Mol Genet 2000;9:3009–3018.
- Rahi JS, Cable N. Severe visual impairment and blindness in children in the UK. Lancet 2003;362:1359–1365.