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Neuronal migration disorders: Focus on the cytoskeleton and epilepsy Tekijä Melissa A. Stouffer, Jeffrey A. Golden, Fiona Francis

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Hippocampal Abnormalities and Enhanced Excitability in a Murine Model of Human Lissencephaly Tekijä Mark W. Fleck, Shinji Hirotsune, Michael J. Gambello, Emily Phillips‐Tansey, Gregory Suares, Ronald F. Mervis, Anthony Wynshaw‐Boris, Chris J. McBain

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Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias Tekijä Mitsuhiro eKato, Mitsuhiro eKato

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Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration Tekijä Orly Reiner, Urs Albrecht, Michal Gordon, KA Chianese, Chen Khuan Wong, O. Gal-Gerber, Tamar Sapir, LD Siracusa, Arthur M. Buchberg, C. Thomas Caskey

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Malformations of cortical development and epilepsy. Tekijä Richard J. Leventer, Renzo Guerrini, William B. Dobyns

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa Tekijä Lori S. Sullivan, John R. Heckenlively, Sara J. Bowne, Jianping Zuo, Yoshihide Hayashizaki, Andreas Gal, Michael J. Denton, Chris F. Inglehearn, Susan H. Blanton, Stephen P. Daiger

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Multiple Dose-Dependent Effects of<i>Lis1</i>on Cerebral Cortical Development Tekijä Michael J. Gambello, Dawn L. Darling, Jessica Yingling, Teruyuki Tanaka, Joseph G. Gleeson, Anthony Wynshaw‐Boris

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A Genetic Animal Model of Human Neocortical Heterotopia Associated with Seizures Tekijä Kevin M. Lee, Frank Schottler, Jennifer L. Collins, Giuseppe Lanzino, Daniel E. Couture, Anand N. Rao, Ken-ichiro Hiramatsu, Yasunobu Goto, Seung‐Chyul Hong, Hakan Caner, Haruaki Yamamoto, Zong‐Fu Chen, Edward H. Bertram, Stuart S. Berr, Reed A. Omary, Heidi Scrable, Theodore Jackson, John C. Goble, Leonard M. Eisenman

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Pathophysiological analyses of cortical malformation using gyrencephalic mammals Tekijä Kosuke Masuda, Tomohisa Toda, Yohei Shinmyo, Haruka Ebisu, Yoshio Hoshiba, Mayu Wakimoto, Yoshie Ichikawa, Hiroshi Kawasaki

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Molecular genetics of human primary microcephaly: an overview Tekijä Muhammad Faheem, Muhammad Imran Naseer, Mahmood Rasool, Adeel Chaudhary, Taha Kumosani, Asad Muhammad Ilyas, Peter Natesan Pushparaj, Farid Ahmed, Hussein Algahtani, Mohammad H. Al-Qahtani, Hasan Saleh Jamal

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Walker-Warburg syndrome Tekijä Jiri Vajsar, Harry Schachter

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Prenatal diagnosis of cobblestone lissencephaly associated with Walker–Warburg syndrome based on a specific sonographic pattern Tekijä Audrey Lacalm, Béatrice Nadaud, Mona Massoud, Audrey Putoux, P. Gaucherand, Laurent Guibaud

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The evolving doublecortin (DCX) superfamily Tekijä Orly Reiner, Frédéric M. Coquelle, Bastian Peter, Talia Levy, Anna Kaplan, Tamar Sapir, Irit Orr, Naama Barkai, Gregor Eichele, Sven Bergmann

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Mowat-Wilson syndrome: neurological and molecular study in seven patients Tekijä José Albino da Paz, Chong Ae Kim, Michael Goossens, Irina Giurgea, Maria Joaquina Marques‐Dias

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Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1 Tekijä Aruto Yoshida, Kazuhiro Kobayashi, Hiroshi Manya, Kiyomi Taniguchi, Hiroki Kano, Mamoru Mizuno, Toshiyuki Inazu, Hideyo Mitsuhashi, Seiichiro Takahashi, Makoto Takeuchi, Ralf Herrmann, Volker Straub, Beril Talim, Thomas Voit, Haluk Topaloğlu, Tatsushi Toda, Tamao Endo

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Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation Tekijä Nathaniel H. Robin, Clare Taylor, Donna M. McDonald‐McGinn, Elaine H. Zackai, Peter M. Bingham, Kevin Collins, Dawn Earl, Deepak Gill, Tiziana Granata, Renzo Guerrini, Naomi Katz, Virginia Kimonis, Jean‐Pierre Lin, David R. Lynch, Shehla Mohammed, R. Massey, Marie McDonald, R. Curtis Rogers, Miranda Splitt, Cathy A. Stevens, Marc Tischkowitz, Neil Stoodley, Richard J. Leventer, Daniela T. Pilz, William B. Dobyns

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Inactivation of<i>Arx</i>, the Murine Ortholog of the X-Linked Lissencephaly with Ambiguous Genitalia Gene, Leads to Severe Disorganization of the Ventral Telencephalon with Impair... Tekijä Elena Colombo, Patrick Collombat, Gaia Colasante, Marta Bianchi, Jason E. Long, Ahmed Mansouri, John L.R. Rubenstein, Vania Broccoli

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New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum Tekijä Nadia Bahi‐Buisson, Isabelle Souville, Franck J. Fourniol, Aurélie Toussaint, Carolyn A. Moores, Anne Houdusse, Jean Yves Lemaitre, Karine Poirier, Reham Khalaf‐Nazzal, Marie Hully, Pierre Louis Léger, Caroline Elie, Nathalie Boddaert, Chérif Beldjord, Jamel Chelly, Fiona Francis

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Presenilin-1 deficiency leads to loss of Cajal–Retzius neurons and cortical dysplasia similar to human type 2 lissencephaly Tekijä Dieter Hartmann, Bart De Strooper, Paul Säftig

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Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency Tekijä Catherine Coffinier, Sandy Y. Chang, Chika Nobumori, Yiping Tu, Emily Farber, Julia I. Toth, Loren G. Fong, Stephen G. Young

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