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There are 6413 results for: content related to: Sodium channels and the neurobiology of epilepsy

  1. You have free access to this content
    Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects

    The Journal of Physiology

    Volume 588, Issue 11, June 2010, Pages: 1841–1848, Miriam H. Meisler, Janelle E. O’Brien and Lisa M. Sharkey

    Version of Record online : 28 MAY 2010, DOI: 10.1113/jphysiol.2010.188482

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    Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures

    Genes, Brain and Behavior

    Volume 11, Issue 2, March 2012, Pages: 170–176, Y.-W. Shi, M.-J. Yu, Y.-S. Long, B. Qin, N. He, H. Meng, X.-R. Liu, W.-Y. Deng, M.-M. Gao, Y.-H. Yi, B.-M. Li and W.-P. Liao

    Version of Record online : 14 DEC 2011, DOI: 10.1111/j.1601-183X.2011.00756.x

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    Sodium channel SCN1A and epilepsy: Mutations and mechanisms

    Epilepsia

    Volume 51, Issue 9, September 2010, Pages: 1650–1658, Andrew Escayg and Alan L. Goldin

    Version of Record online : 28 MAY 2010, DOI: 10.1111/j.1528-1167.2010.02640.x

  4. SCN1A mutations and epilepsy

    Human Mutation

    Volume 25, Issue 6, June 2005, Pages: 535–542, John C. Mulley, Ingrid E. Scheffer, Steven Petrou, Leanne M. Dibbens, Samuel F. Berkovic and Louise A. Harkin

    Version of Record online : 6 MAY 2005, DOI: 10.1002/humu.20178

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    Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome

    Epilepsia

    Volume 54, Issue 9, September 2013, Pages: e122–e126, John C. Mulley, Bree Hodgson, Jacinta M. McMahon, Xenia Iona, Susannah Bellows, Saul A Mullen, Kevin Farrell, Mark Mackay, Lynette Sadleir, Andrew Bleasel, Deepak Gill, Richard Webster, Elaine C. Wirrell, Michael Harbord, Sanyjay Sisodiya, Eva Andermann, Sara Kivity, Samuel F. Berkovic, Ingrid E. Scheffer and Leanne M. Dibbens

    Version of Record online : 29 JUL 2013, DOI: 10.1111/epi.12323

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    SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

    Epilepsia

    Volume 50, Issue 7, July 2009, Pages: 1670–1678, Carla Marini, Ingrid E. Scheffer, Rima Nabbout, Davide Mei, Kathy Cox, Leanne M. Dibbens, Jacinta M. McMahon, Xenia Iona, Rochio Sanchez Carpintero, Maurizio Elia, Maria Roberta Cilio, Nicola Specchio, Lucio Giordano, Pasquale Striano, Elena Gennaro, J. Helen Cross, Sara Kivity, Miriam Y. Neufeld, Zaid Afawi, Eva Andermann, Daniel Keene, Olivier Dulac, Federico Zara, Samuel F. Berkovic, Renzo Guerrini and John C. Mulley

    Version of Record online : 12 MAR 2009, DOI: 10.1111/j.1528-1167.2009.02013.x

  7. Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures

    Clinical Genetics

    Volume 80, Issue 2, August 2011, Pages: 191–195, M Bartnik, A Chun-Hui Tsai, Z Xia, SW Cheung and P Stankiewicz

    Version of Record online : 2 AUG 2010, DOI: 10.1111/j.1399-0004.2010.01526.x

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    Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Nav1.1

    Epilepsia

    Volume 51, Issue 9, September 2010, Pages: 1669–1678, Wei-Ping Liao, Yi-Wu Shi, Yue-Sheng Long, Yang Zeng, Tian Li, Mei-Juan Yu, Tao Su, Ping Deng, Zhi-Gang Lei, Shu-Jun Xu, Wei-Yi Deng, Xiao-Rong Liu, Wei-Wen Sun, Yong-Hong Yi, Zao C. Xu and Shumin Duan

    Version of Record online : 7 JUN 2010, DOI: 10.1111/j.1528-1167.2010.02645.x

  9. You have full text access to this OnlineOpen article
    Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss

    Genes, Brain and Behavior

    Volume 8, Issue 7, October 2009, Pages: 699–713, F. E. Mackenzie, A. Parker, N. J. Parkinson, P. L. Oliver, D. Brooker, P. Underhill, V. A. Lukashkina, A. N. Lukashkin, C. Holmes and S. D. M. Brown

    Version of Record online : 22 JUN 2009, DOI: 10.1111/j.1601-183X.2009.00514.x

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    Abstracts

    Epilepsia

    Volume 56, Issue S1, December 2015, Pages: 3–263,

    Version of Record online : 30 NOV 2015, DOI: 10.1111/epi.13241

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    High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy

    Epilepsia

    Volume 51, Issue 4, April 2010, Pages: 694–698, Andrew Makoff, Teck Lai, Catherine Barratt, Antonio Valentin, Nick Moran, Philip Asherson and Lina Nashef

    Version of Record online : 22 DEC 2009, DOI: 10.1111/j.1528-1167.2009.02473.x

  12. Genes and loci involved in febrile seizures and related epilepsy syndromes

    Human Mutation

    Volume 27, Issue 5, May 2006, Pages: 391–401, Dominique Audenaert, Christine Van Broeckhoven and Peter De Jonghe

    Version of Record online : 20 MAR 2006, DOI: 10.1002/humu.20279

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    The SCN1A variant database: a novel research and diagnostic tool

    Human Mutation

    Volume 30, Issue 10, October 2009, Pages: E904–E920, Lieve RF Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets, Tine Van Dyck, Tine Deconinck, Albena Jordanova and Peter De Jonghe

    Version of Record online : 7 JUL 2009, DOI: 10.1002/humu.21083

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    26th IEC PROCEEDINGS 26th International Epilepsy Congress Paris, France, August 28th– September 1st 2005

    Epilepsia

    Volume 46, Issue s6, September 2005, Pages: 3–415,

    Version of Record online : 30 AUG 2005, DOI: 10.1111/j.1528-1167.2005.460602.x

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    Molecular genetics of Dravet syndrome

    Developmental Medicine & Child Neurology

    Volume 53, Issue s2, April 2011, Pages: 7–10, PETER DE JONGHE

    Version of Record online : 19 APR 2011, DOI: 10.1111/j.1469-8749.2011.03965.x

  16. You have free access to this content
    NaV1.1 channels and epilepsy

    The Journal of Physiology

    Volume 588, Issue 11, June 2010, Pages: 1849–1859, William A. Catterall, Franck Kalume and John C. Oakley

    Version of Record online : 28 MAY 2010, DOI: 10.1113/jphysiol.2010.187484

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    SCN1A testing for epilepsy: Application in clinical practice

    Epilepsia

    Volume 54, Issue 5, May 2013, Pages: 946–952, Shinichi Hirose, Ingrid E. Scheffer, Carla Marini, Peter De Jonghe, Eva Andermann, Alica M. Goldman, Marcelo Kauffman, Nigel C. K. Tan, Daniel H. Lowenstein, Sanjay M. Sisodiya, Ruth Ottman, Samuel F. Berkovic and The Genetics Commission of the International League Against Epilepsy

    Version of Record online : 15 APR 2013, DOI: 10.1111/epi.12168

  18. Scn1a dysfunction alters behavior but not the effect of stress on seizure response

    Genes, Brain and Behavior

    Volume 15, Issue 3, March 2016, Pages: 335–347, N. T. Sawyer, A. W. Helvig, C. D. Makinson, M. J. Decker, G. N. Neigh and A. Escayg

    Version of Record online : 21 JAN 2016, DOI: 10.1111/gbb.12281

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    Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations

    Epilepsia

    Volume 45, Issue 2, February 2004, Pages: 149–158, Paolo Bonanni, Michela Malcarne, Francesca Moro, Pierangelo Veggiotti, Daniela Buti, Anna Rita Ferrari, Elena Parrini, Davide Mei, Anna Volzone, Federico Zara, Sarah E. Heron, Laura Bordo, Carla Marini and Renzo Guerrini

    Version of Record online : 26 JAN 2004, DOI: 10.1111/j.0013-9580.2004.04303.x

  20. You have free access to this content
    Embryonic and larval expression of zebrafish voltage-gated sodium channel α-subunit genes

    Developmental Dynamics

    Volume 235, Issue 7, July 2006, Pages: 1962–1973, Alicia E. Novak, Alison D. Taylor, Ricardo H. Pineda, Erika L. Lasda, Melissa A. Wright and Angeles B. Ribera

    Version of Record online : 13 APR 2006, DOI: 10.1002/dvdy.20811