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There are 12109 results for: content related to: Altered sleep regulation in a mouse model of SCN1A - derived genetic epilepsy with febrile seizures plus ( GEFS +)

  1. You have free access to this content
    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

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    Methylphenidate improves learning impairments and hyperthermia-induced seizures caused by an Scn1a mutation

    Epilepsia

    Volume 55, Issue 10, October 2014, Pages: 1558–1567, Iori Ohmori, Nozomi Kawakami, Sumei Liu, Haijiao Wang, Ikuko Miyazaki, Masato Asanuma, Hiroyuki Michiue, Hideki Matsui, Tomoji Mashimo and Mamoru Ouchida

    Version of Record online : 25 AUG 2014, DOI: 10.1111/epi.12750

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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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    Co-occurring malformations of cortical development and SCN1A gene mutations

    Epilepsia

    Volume 55, Issue 7, July 2014, Pages: 1009–1019, Carmen Barba, Elena Parrini, Roland Coras, Anna Galuppi, Dana Craiu, Gerhard Kluger, Antonia Parmeggiani, Tom Pieper, Thomas Schmitt-Mechelke, Pasquale Striano, Flavio Giordano, Ingmar Blumcke and Renzo Guerrini

    Version of Record online : 5 JUN 2014, DOI: 10.1111/epi.12658

  5. Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome

    Epilepsia

    Volume 58, Issue 2, February 2017, Pages: 282–290, Atsushi Ishii, Joseph C. Watkins, Debbie Chen, Shinichi Hirose and Michael F. Hammer

    Version of Record online : 24 DEC 2016, DOI: 10.1111/epi.13639

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    The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: A population-based study from 2004 to 2009

    Epilepsia

    Volume 56, Issue 4, April 2015, Pages: e36–e39, Allan Bayat, Helle Hjalgrim and Rikke S. Møller

    Version of Record online : 16 MAR 2015, DOI: 10.1111/epi.12927

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    Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine

    Epilepsia

    Volume 54, Issue 5, May 2013, Pages: 927–935, Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza and Antonio Gambardella

    Version of Record online : 8 FEB 2013, DOI: 10.1111/epi.12123

  8. Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome

    Epilepsia

    Jeffrey D. Calhoun, Nicole A. Hawkins, Nicole J. Zachwieja and Jennifer A. Kearney

    Version of Record online : 28 MAY 2017, DOI: 10.1111/epi.13811

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    SCN8A encephalopathy: Research progress and prospects

    Epilepsia

    Volume 57, Issue 7, July 2016, Pages: 1027–1035, Miriam H. Meisler, Guy Helman, Michael F. Hammer, Brandy E. Fureman, William D. Gaillard, Alan L. Goldin, Shinichi Hirose, Atsushi Ishii, Barbara L. Kroner, Christoph Lossin, Heather C. Mefford, Jack M. Parent, Manoj Patel, John Schreiber, Randall Stewart, Vicky Whittemore, Karen Wilcox, Jacy L Wagnon, Phillip L. Pearl, Adeline Vanderver and Ingrid E. Scheffer

    Version of Record online : 8 JUN 2016, DOI: 10.1111/epi.13422

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    SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability

    Epilepsia

    Volume 56, Issue 3, March 2015, Pages: 431–438, Weijing Kong, Yujia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jingmin Wang, Ye Wu, Yuehua Zhang, Xiru Wu and Yuwu Jiang

    Version of Record online : 26 FEB 2015, DOI: 10.1111/epi.12925

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    Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities

    Epilepsia

    Volume 48, Issue 9, September 2007, Pages: 1678–1685, Carla Marini, Davide Mei, Teresa Temudo, Anna Rita Ferrari, Daniela Buti, Charlotte Dravet, Ana I. Dias, Ana Moreira, Eulalia Calado, Stefano Seri, Brian Neville, Juan Narbona, Evan Reid, Roberto Michelucci, Federico Sicca, Helen J. Cross and Renzo Guerrini

    Version of Record online : 11 JUN 2007, DOI: 10.1111/j.1528-1167.2007.01122.x

  12. Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features

    Epilepsia

    Volume 58, Issue 3, March 2017, Pages: e44–e48, Danah Aljaafari, Alfonso Fasano, Fábio A. Nascimento, Anthony E. Lang and Danielle M. Andrade

    Version of Record online : 10 FEB 2017, DOI: 10.1111/epi.13692

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    Genetic epileptic encephalopathies: Is all written into the DNA?

    Epilepsia

    Volume 54, Issue s8, November 2013, Pages: 22–26, Pasquale Striano, Peter de Jonghe and Federico Zara

    Version of Record online : 13 NOV 2013, DOI: 10.1111/epi.12419

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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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    Dravet syndrome—From epileptic encephalopathy to channelopathy

    Epilepsia

    Volume 55, Issue 7, July 2014, Pages: 979–984, Andreas Brunklaus and Sameer M. Zuberi

    Version of Record online : 16 MAY 2014, DOI: 10.1111/epi.12652

  16. Comparison and optimization of in silico algorithms for predicting the pathogenicity of sodium channel variants in epilepsy

    Epilepsia

    Volume 58, Issue 7, July 2017, Pages: 1190–1198, Katherine D. Holland, Thomas M. Bouley and Paul S. Horn

    Version of Record online : 18 MAY 2017, DOI: 10.1111/epi.13798

  17. The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

    Human Mutation

    Volume 36, Issue 6, June 2015, Pages: 573–580, Heng Meng, Hai-Qing Xu, Lu Yu, Guo-Wang Lin, Na He, Tao Su, Yi-Wu Shi, Bin Li, Jie Wang, Xiao-Rong Liu, Bin Tang, Yue-Sheng Long, Yong-Hong Yi and Wei-Ping Liao

    Version of Record online : 13 APR 2015, DOI: 10.1002/humu.22782

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    Purinergic control of hippocampal circuit hyperexcitability in Dravet syndrome

    Epilepsia

    Volume 55, Issue 2, February 2014, Pages: 245–255, Feng Gu, Anupam Hazra, Ahmad Aulakh and Jokūbas Žiburkus

    Version of Record online : 13 JAN 2014, DOI: 10.1111/epi.12487

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    Dravet syndrome: New potential genetic modifiers, imaging abnormalities, and ictal findings

    Epilepsia

    Volume 54, Issue 9, September 2013, Pages: 1577–1585, Eija Gaily, Anna-Kaisa Anttonen, Leena Valanne, Elina Liukkonen, Ann-Liz Träskelin, Anne Polvi, Markus Lommi, Mikko Muona, Kai Eriksson and Anna-Elina Lehesjoki

    Version of Record online : 28 JUN 2013, DOI: 10.1111/epi.12256

  20. 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