Canlyniadau Chwilio - Richard J. Leventer
- Dangos 1 - 20 canlyniadau o 68
- Ewch i'r Dudalen Nesaf
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Malformations of cortical development and epilepsy. gan Richard J. Leventer, Renzo Guerrini, William B. Dobyns
Cyhoeddwyd 2008Artigo -
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Malformations of cortical development and epilepsy gan Richard J. Leventer, Renzo Guerrini, William B. Dobyns
Cyhoeddwyd 2008Artigo -
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A Neuropsychological Profile for Agenesis of the Corpus Callosum? Cognitive, Academic, Executive, Social, and Behavioral Functioning in School-Age Children gan Vanessa Siffredi, Vicki Anderson, Alissandra McIlroy, Amanda Wood, Richard J. Leventer, Megan Spencer‐Smith
Cyhoeddwyd 2018Artigo -
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Pontine Tegmental Cap Dysplasia: MR Imaging and Diffusion Tensor Imaging Features of Impaired Axonal Navigation gan Patrice Jissendi‐Tchofo, Dan Doherty, George McGillivray, Robert F. Hevner, Dennis Shaw, Gisele E. Ishak, Richard J. Leventer, A. James Barkovich
Cyhoeddwyd 2008Artigo -
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Whole exome sequencing in family trios reveals<i>de novo</i>mutations in<i>PURA</i>as a cause of severe neurodevelopmental delay and learning disability gan David Hunt, Richard J. Leventer, Cas Simons, Ryan J. Taft, Kathryn J. Swoboda, M. L. Gawne‐Cain, Alex Magee, Peter D. Turnpenny, Diana Baralle
Cyhoeddwyd 2014Artigo -
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Gradient of brain mosaic <i>RHEB</i> variants causes a continuum of cortical dysplasia gan Wei Shern Lee, Sara Baldassari, Mathilde Chipaux, Homa Adle‐Biassette, Sarah Stephenson, Wirginia Maixner, A. Simon Harvey, Paul J. Lockhart, Stéphanie Baulac, Richard J. Leventer
Cyhoeddwyd 2021Artigo -
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Detection of Epileptogenic Cortical Malformations with Surface-Based MRI Morphometry gan Thomas Thesen, Brian T. Quinn, Chad Carlson, Orrin Devinsky, Jonathan M. DuBois, Carrie R. McDonald, Jacqueline A. French, Richard J. Leventer, Olga Felsovalyi, Xiuyuan Wang, Eric Halgren, Ruben Kuzniecky
Cyhoeddwyd 2011Artigo -
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<i>DARS</i> -associated leukoencephalopathy can mimic a steroid-responsive neuroinflammatory disorder gan Nicole I. Wolf, Camilo Toro, Ilya Kister, Kartikasalwah Abd Latif, Richard J. Leventer, Amy Pizzino, Cas Simons, Truus E. M. Abbink, Ryan J. Taft, Marjo S. van der Knaap, Adeline Vanderver
Cyhoeddwyd 2014Artigo -
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Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes gan Katherine R. Smith, Catherine J. Bromhead, Michael S. Hildebrand, A. Eliot Shearer, Paul J. Lockhart, Hossein Najmabadi, Richard J. Leventer, George McGillivray, David J. Amor, Richard J. Smith, Melanie Bahlo
Cyhoeddwyd 2011Artigo -
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Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia gan Naomichi Matsumoto, Richard J. Leventer, Julie A. Kuc, Stephanie K. Mewborn, L. Dudlicek, Melissa B. Ramocki, Daniela T. Pilz, Patti L. Mills, Soma Das, M. Elizabeth Ross, David H. Ledbetter, William B. Dobyns
Cyhoeddwyd 2001Artigo -
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The surgically remediable syndrome of epilepsy associated with bottom-of-sulcus dysplasia gan A. Simon Harvey, Simone Mandelstam, Wirginia Maixner, Richard J. Leventer, Mira Semmelroch, Duncan MacGregor, Renate M. Kalnins, Yuliya Perchyonok, Gregory J. Fitt, Sarah Barton, Michael Kean, Gavin Fabinyi, Graeme D. Jackson
Cyhoeddwyd 2015Artigo -
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Definitions and classification of malformations of cortical development: practical guidelines gan Mariasavina Severino, Ana Filipa Geraldo, Norbert Utz, Domenico Tortora, Ivana Pogledić, Włodzimierz Klonowski, Fabio Triulzi, Filippo Arrigoni, Kshitij Mankad, Richard J. Leventer, Grazia M.S. Mancini, James Barkovich, Maarten H. Lequin, Andrea Rossi
Cyhoeddwyd 2020Revisão -
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Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder gan Margherita Nosadini, Gülay Alper, Catherine J. Riney, Leslie Benson, Shekeeb S. Mohammad, Sudarshini Ramanathan, Melinda Nolan, Richard Appleton, Richard J. Leventer, Kumaran Deiva, Fabienne Brilot, Mark Gorman, Amy Waldman, Brenda Banwell, Russell C. Dale
Cyhoeddwyd 2016Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Medicine
Gene
Genetics
Neuroscience
Pathology
Epilepsy
Psychiatry
Mutation
Phenotype
Internal medicine
Pediatrics
Polymicrogyria
Radiology
Anatomy
Cortical dysplasia
Lissencephaly
Missense mutation
Psychology
Dysplasia
Magnetic resonance imaging
Exome sequencing
Biochemistry
Disease
Neuroimaging
Exome
Genotype
Germline mutation
Pregnancy
Somatic cell