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Neurology|August 26, 1998
Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformationR Guerrini, W B DobynsNeurologia (Barcelona, Spain)|June 24, 1999
Epilepsy and malformations of the cerebral cortexR Guerrini, R Canapicchi, W B DobynsNeurology|February 26, 2000
Bilateral frontal polymicrogyria: a newly recognized brain malformation syndromeR Guerrini, A J Barkovich, L Sztriha, et al.Human Molecular Genetics|July 21, 1998
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defectsK Sossey-Alaoui, A J Hartung, R Guerrini, et al.American Journal of Human Genetics|August 1, 1997
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopiaJ M Fink, W B Dobyns, R Guerrini, et al.Neuropediatrics|December 19, 2003
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literatureM Rossi, R Guerrini, W B Dobyns, et al.Neurology|September 30, 2005
A developmental and genetic classification for malformations of cortical developmentA J Barkovich, R I Kuzniecky, G D Jackson, et al.Neurology|January 12, 2002
Classification system for malformations of cortical development: update 2001A J Barkovich, R I Kuzniecky, G D Jackson, et al.Neurology|October 29, 2003
Mosaic mutations of the LIS1 gene cause subcortical band heterotopiaF Sicca, A Kelemen, P Genton, et al.Pageof 64