Zoekresultaten

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

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Intracranial evaluation of the epileptogenic zone in regional infrasylvian polymicrogyria door Georgia Ramantani, Laurent Koessler, Sophie Colnat‐Coulbois, Jean‐Pierre Vignal, Jean Isnard, Hélène Catenoix, Jacques Jonas, Josef Zentner, Andreas Schulze‐Bonhage, Louis Georges Maillard

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

Sulthiame add‐on therapy in children with focal epilepsies associated with encephalopathy related to electrical status epilepticus during slow sleep (ESES) door Natalio Fejerman, Roberto Caraballo, Ricardo Cersósimo, S.M. Ferraro, Santiago Galicchio, Hernán Amartino

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The histopathology of polymicrogyria: a series of 71 brain autopsy studies door Anna Jansen, Yves Robitaille, Mrinalini Honavar, Nandini Mullatti, Richard J. Leventer, Eva Andermann, Frédérick Andermann, Waney Squier

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

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Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study door Ghayda Mirzaa, Valerio Conti, Andrew E. Timms, Christopher D. Smyser, Sarah Ahmed, Melissa Carter, Sarah Barnett, Robert B. Hufnagel, Amy Goldstein, Yoko Narumi‐Kishimoto, Carissa Olds, Sarah Collins, Kathreen Johnston, Jean‐François Deleuze, Patrick Nitschké, Kathryn Friend, Catharine Harris, Allison L. Goetsch, Beth Martin, Evan A. Boyle, Elena Parrini, Davide Mei, Lorenzo Tattini, Anne Slavotinek, Ed Blair, Christopher Barnett, Jay Shendure, Jamel Chelly, William B. Dobyns, Renzo Guerrini

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Interpersonal traits of psychopathy linked to reduced integrity of the uncinate fasciculus door Richard C. Wolf, Maia S. Pujara, Julian C. Motzkin, Joseph P. Newman, Kent A. Kiehl, Jean Decety, David S. Kosson, Michael Koenigs

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MR susceptibility weighted imaging (SWI) complements conventional contrast enhanced T1 weighted MRI in characterizing brain abnormalities of Sturge‐Weber Syndrome door Jiani Hu, Yingjian Yu, Csaba Juhász, Zhifeng Kou, Yang Xuan, Zahid Latif, Kohsuke Kudo, Harry T. Chugani, E. Mark Haacke

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Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation door 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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Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients door Robert L. Conway, Barry D. Pressman, William B. Dobyns, Moise Danielpour, John Lee, Pedro A. Sanchez‐Lara, Merlin G. Butler, Elaine H. Zackai, Lindsey Campbell, Sulagna C. Saitta, Carol L. Clericuzio, Jeff M. Milunsky, H. Eugene Hoyme, Joseph T.C. Shieh, John B. Moeschler, Barbara F. Crandall, Julie Lauzon, David Viskochil, Brian Harding, John M. Graham

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Occipital Lobe Developmental Malformations and Epilepsy: Clinical Spectrum, Treatment, and Outcome door Ruben Kuzniecky, Frank Gilliam, Richard Morawetz, Edward Faught, Cheryl A. Palmer, Lorie Black

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Intralesional recordings and epileptogenic zone in focal polymicrogyria door Francine Chassoux, Elisabeth Landré, S. Rodrigo, F. Beuvon, Baris Turak, Franck Semah, Bertrand Devaux

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Periventricular nodular heterotopia with overlying polymicrogyria door Gretchen Wieck, Richard J. Leventer, Waney M. Squier, Anna Jansen, Eva Andermann, François Dubeau, Anna Ramazzotti, Renzo Guerrini, William B. Dobyns

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Electrical source imaging in cortical malformation–related epilepsy: A prospective <scp>EEG</scp>‐<scp>SEEG</scp> concordance study door Estelle Rikir, Laurent Koessler, Martine Gavaret, Fabrice Bartoloméi, Sophie Colnat‐Coulbois, Jean‐Pierre Vignal, Hervé Vespignani, Georgia Ramantani, Louis Maillard

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Genetic Malformations of the Cerebral Cortex and Epilepsy door Renzo Guerrini

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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations door Michael Field, Ingrid E. Scheffer, Deepak Gill, Meredith Wilson, Louise Christie, Marie Shaw, Alison Gardner, Georgie C. Glubb, Lynne Hobson, Mark Corbett, Kathryn Friend, Saffron A.G. Willis‐Owen, Jozef Gécz

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Malformations of Cortical Development door Trudy Pang, Ramin Atefy, Volney Sheen

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Mechanics of the brain: perspectives, challenges, and opportunities door Alain Goriely, M.G.D. Geers, Gerhard A. Holzapfel, Jayaratnam Jayamohan, Antoine Jérusalem, Sivabal Sivaloganathan, Waney Squier, J.A.W. van Dommelen, Sarah L. Waters, Ellen Kuhl

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RTTN Mutations Link Primary Cilia Function to Organization of the Human Cerebral Cortex door Sima Kheradmand Kia, Elly Verbeek, Erik Engelen, Rachel Schot, Raymond A. Poot, I.F.M. de Coo, Maarten H. Lequin, Cathryn Poulton, Farzin Pourfarzad, Frank Grosveld, António Brehm, Marie‐Claire Y. de Wit, Renske Oegema, William B. Dobyns, Frans W. Verheijen, Grazia M.S. Mancini

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