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	61.	Sonographic diagnosis of cerebral malformations. Part 3: agenesis of the corpus callosum - migration disorders. [electronic resource] by Deeg, K-H Producer: 20110815 In: Ultraschall in der Medizin (Stuttgart, Germany : 1980) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Post-natal investigations: management and prognosis for fetuses with CNS anomalies identified in utero excluding neurosurgical problems. [electronic resource] by Mighell, Amal S Johnstone, Ed D Levene, Malcolm Producer: 20090618 In: Prenatal diagnosis vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes. [electronic resource] by Pawlisz, Ashley S Feng, Yuanyi Producer: 20120214 In: PLoS biology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. [electronic resource] by Conti, Valerio Carabalona, Aurelie Pallesi-Pocachard, Emilie Parrini, Elena Leventer, Richard J Buhler, Emmanuelle McGillivray, George Michel, François J Striano, Pasquale Mei, Davide Watrin, Françoise Lise, Stefano Pagnamenta, Alistair T Taylor, Jenny C Kini, Usha Clayton-Smith, Jill Novara, Francesca Zuffardi, Orsetta Dobyns, William B Scheffer, Ingrid E Robertson, Stephen P Berkovic, Samuel F Represa, Alfonso Keays, David A Cardoso, Carlos Guerrini, Renzo Producer: 20131231 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly. [electronic resource] by Kerjan, Geraldine Gleeson, Joseph G Producer: 20080225 In: Trends in genetics : TIG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	[Neurocristopathies: a high incidence of cerebral dysgenesis in patients with Hirschsprung's disease]. [electronic resource] by Carrascosa-Romero, M C Fernández-Córdoba, M S Gonzálvez-Piñera, J Gutiérrez-Junquera, C Pardal-Fernández, J M Producer: 20080403 In: Revista de neurologia vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	67.	Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. [electronic resource] by Burbridge, T J Wang, Y Volz, A J Peschansky, V J Lisann, L Galaburda, A M Lo Turco, J J Rosen, G D Producer: 20080721 In: Neuroscience vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Post-section recruitment of epileptiform discharges in electrocorticography during callosotomy in 48 patients with Lennox-Gastaut syndrome. [electronic resource] by Lin, Ji-Ho Kwan, Shang-Yeong Producer: 20120531 In: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III. [electronic resource] by Juric-Sekhar, Gordana Kapur, Raj P Glass, Ian A Murray, Mitzi L Parnell, Shawn E Hevner, Robert F Producer: 20110701 In: Acta neuropathologica vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Heat shock factor 2 is a stress-responsive mediator of neuronal migration defects in models of fetal alcohol syndrome. [electronic resource] by El Fatimy, Rachid Miozzo, Federico Le Mouël, Anne Abane, Ryma Schwendimann, Leslie Sabéran-Djoneidi, Délara de Thonel, Aurélie Massaoudi, Illiasse Paslaru, Liliana Hashimoto-Torii, Kazue Christians, Elisabeth Rakic, Pasko Gressens, Pierre Mezger, Valérie Producer: 20150330 In: EMBO molecular medicine vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Ethanol inhibition of aspartyl-asparaginyl-beta-hydroxylase in fetal alcohol spectrum disorder: potential link to the impairments in central nervous system neuronal migration. [electronic resource] by de la Monte, Suzanne M Tong, Ming Carlson, Rolf I Carter, Jade J Longato, Lisa Silbermann, Elizabeth Wands, Jack R Producer: 20090528 In: Alcohol (Fayetteville, N.Y.) vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Annual Research Review: Development of the cerebral cortex: implications for neurodevelopmental disorders. [electronic resource] by Rubenstein, John L R Producer: 20110804 In: Journal of child psychology and psychiatry, and allied disciplines vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies. [electronic resource] by Chan, Yiumo Michael Keramaris-Vrantsis, Elizabeth Lidov, Hart G Norton, James H Zinchenko, Natalia Gruber, Helen E Thresher, Randy Blake, Derek J Ashar, Jignya Rosenfeld, Jeffrey Lu, Qi L Producer: 20110301 In: Human molecular genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder. [electronic resource] by Manent, Jean-Bernard Wang, Yu Chang, Yoonjeung Paramasivam, Murugan LoTurco, Joseph J Producer: 20090204 In: Nature medicine vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome. [electronic resource] by Baas, Annette F Gabbett, Michael Rimac, Milan Kansikas, Minttu Raphael, Martine Nievelstein, Rutger Aj Nicholls, Wayne Offerhaus, Johan Bodmer, Danielle Wernstedt, Annekatrin Krabichler, Birgit Strasser, Ulrich Nyström, Minna Zschocke, Johannes Robertson, Stephen P van Haelst, Mieke M Wimmer, Katharina Producer: 20130520 In: European journal of human genetics : EJHG vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse. [electronic resource] by Way, Sharon W McKenna, James Mietzsch, Ulrike Reith, R Michelle Wu, Henry Cheng-Ju Gambello, Michael J Producer: 20090518 In: Human molecular genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Molecular genetics of neuronal migration disorders. [electronic resource] by Liu, Judy S Producer: 20110603 In: Current neurology and neuroscience reports vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)