SEARCH

SEARCH BY CITATION

References

  • Battaglia G, Granata T, Farina L, D’Incerti L, Franceschetti S, Avanzini G. (1997) Periventricular nodular heterotopia: epileptogenic findings. Epilepsia 38:11731182.
  • Battaglia G, Chiapparini L, Franceschetti S, Freri E, Tassi L, Bassanini S, Villani F, Spreafico R, D’Incerti L, Granata T. (2006) Periventricular nodular heterotopia: classification, epileptic history, and genesis of epileptic discharges. Epilepsia 47:8697.
  • Cardoso C, Boys A, Parrini E, Mignon-Ravix C, McMahon JM, Khantane S, Bertini E, Pallesi E, Missirian C, Zuffardi O, Novara F, Villard L, Giglio S, Chabrol B, Slater HR, Moncla A, Scheffer IE, de Wit MC, de Coo IF, Halley DJ, Lequin MH, Mancini GM. (2009) Movement disorder and neuronal migration disorder due to ARFGEF2 mutation. Neurogenetics 10 (4):333336.
  • de Wit MC, Kros JM, Halley DJ, de Coo IF, Verdijk R, Jacobs BC, Mancini GM. (2009) Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects. J Neurol Neurosurg Psychiatry 80:426428.
  • Dubeau F, Tampieri D, Lee N, Andermann E, Carpenter S, Leblanc R, Olivier A, Radtke R, Villemure JG, Andermann F. (1995) Periventricular and subcortical nodular heterotopia. A study of 33 patients. Brain 118:12731287.
  • Ferland RJ, Gaitanis JN, Apse K, Tantravahi U, Walsh CA, Sheen VL. (2006) Periventricular nodular heterotopia and Williams syndrome. Am J Med Genet A 140:13051311.
  • Fox JW, Lamperti ED, Ekşioğlu YZ, Hong SE, Feng Y, Graham DA, Scheffer IE, Dobyns WB, Hirsch BA, Radtke RA, Berkovic SF, Huttenlocher PR, Walsh CA. (1998) Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron 21:13151325.
  • Gressens P, Kosofsky BE, Evrard P. (1992) Cocaine-induced disturbances of corticogenesis in the developing murine brain. Neurosci Lett 140:113116.
  • Guerrini R, Carrozzo R. (2001) Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing. Seizure 10:532543.
  • Guerrini R, Dobyns WB. (1998) Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation. Neurology 51:499503.
  • Guerrini R, Parrini E. (2010) Neuronal migration disorders. Neurobiol Dis 38(2):154166.
  • Humphreys P, Muzumdar DP, Sly LE, Michaud J. (2007) Focal cerebral mantle disruption in fetal hydrocephalus. Pediatr Neurol 36:236243.
  • Kawamura T, Morioka T, Nishio S, Mihara F, Fukui M. (2001) Cerebral abnormalities in lumbosacral neural tube closure defect: MR imaging evaluation. Childs Nerv Syst 17:405410.
  • Kyndt F, Gueffet JP, Probst V, Jaafar P, Legendre A, Le Bouffant F, Toquet C, Roy E, McGregor L, Lynch SA, Newbury-Ecob R, Tran V, Young I, Trochu JN, Le Marec H, Schott JJ. (2007) Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy. Circulation 115:4049.
  • McLone DG, Knepper PA. (1989) The cause of Chiari II malformation: a unified theory. Pediatr Neurosci 15:112.
  • Neal J, Apse K, Sahin M, Walsh CA, Sheen VL. (2006) Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia. Am J Med Genet A 140:16921695.
  • Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R. (2006) Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. Brain 129:18921906.
  • Raymond AA, Fish DR, Stevens JM, Sisodiya SM, Alsanjari N, Shorvon SD. (1994) Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy. J Neurol Neurosurg Psychiatry 57:11951202.
  • Raymond AA, Fish DR, Sisodiya SM, Alsanjari N, Stevens JM, Shorvon SD. (1995) Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patients. Brain 118:629660.
  • Saito S, Kawamura R, Kosho T, Shimizu T, Aoyama K, Koike K, Wada T, Matsumoto N, Kato M, Wakui K, Fukushima Y. (2008) Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36. Am J Med Genet A 146A:28912897.
  • Sheen VL, Topçu M, Berkovic S, Yalnizoglu D, Blatt I, Bodell A, Hill RS, Ganesh VS, Cherry TJ, Shugart YY, Walsh CA. (2003a) Autosomal recessive form of periventricular heterotopia. Neurology 60:11081112.
  • Sheen VL, Wheless JW, Bodell A, Braverman E, Cotter PD, Rauen KA, Glenn O, Weisiger K, Packman S, Walsh CA, Sherr EH. (2003b) Periventricular heterotopia associated with chromosome 5p anomalies. Neurology 60:10331036.
  • Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA. (2004) Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex. Nat Genet 36:6976.