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There are 13959 results for: content related to: Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

  1. You have full text access to this OnlineOpen article
    Tau reduction prevents disease in a mouse model of Dravet syndrome

    Annals of Neurology

    Volume 76, Issue 3, September 2014, Pages: 443–456, Ania L. Gheyara, Ravikumar Ponnusamy, Biljana Djukic, Ryan J. Craft, Kaitlyn Ho, Weikun Guo, Mariel M. Finucane, Pascal E. Sanchez and Lennart Mucke

    Version of Record online : 13 AUG 2014, DOI: 10.1002/ana.24230

  2. You have full text access to this OnlineOpen article
    Screening of conventional anticonvulsants in a genetic mouse model of epilepsy

    Annals of Clinical and Translational Neurology

    Nicole A. Hawkins, Lyndsey L. Anderson, Tracy S. Gertler, Linda Laux, Alfred L. George Jr. and Jennifer A. Kearney

    Version of Record online : 26 APR 2017, DOI: 10.1002/acn3.413

  3. You have free access to this content
    Mapping genetic modifiers of survival in a mouse model of Dravet syndrome

    Genes, Brain and Behavior

    Volume 13, Issue 2, February 2014, Pages: 163–172, A. R. Miller, N. A. Hawkins, C. E. McCollom and J. A. Kearney

    Version of Record online : 14 NOV 2013, DOI: 10.1111/gbb.12099

  4. 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

  5. You have full text access to this OnlineOpen article
    Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novoSCN1A Mutations in Children with Dravet Syndrome

    Human Mutation

    Volume 36, Issue 9, September 2015, Pages: 861–872, Xiaojing Xu, Xiaoxu Yang, Qixi Wu, Aijie Liu, Xiaoling Yang, Adam Yongxin Ye, August Yue Huang, Jiarui Li, Meng Wang, Zhe Yu, Sheng Wang, Zhichao Zhang, Xiru Wu, Liping Wei and Yuehua Zhang

    Version of Record online : 24 JUL 2015, DOI: 10.1002/humu.22819

  6. You have free access to this content
    Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome

    Epilepsia

    Volume 53, Issue 7, July 2012, Pages: 1140–1145, Dezhi Cao, Hideyuki Ohtani, Ikuo Ogiwara, Sanae Ohtani, Yukitoshi Takahashi, Kazuhiro Yamakawa and Yushi Inoue

    Version of Record online : 11 MAY 2012, DOI: 10.1111/j.1528-1167.2012.03497.x

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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

  8. Molecular Genetics of Dravet Syndrome

    Standard Article

    eLS

    Sarah Weckhuysen, Arvid Suls and Peter Jonghe

    Published Online : 15 MAR 2012, DOI: 10.1002/9780470015902.a0023846

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    A Screening test for the prediction of Dravet syndrome before one year of age

    Epilepsia

    Volume 49, Issue 4, April 2008, Pages: 626–633, Junri Hattori, Mamoru Ouchida, Junko Ono, Susumu Miyake, Satoshi Maniwa, Nobuyoshi Mimaki, Yoko Ohtsuka and Iori Ohmori

    Version of Record online : 11 DEC 2007, DOI: 10.1111/j.1528-1167.2007.01475.x

  10. Parental SCN1A mutation mosaicism in familial Dravet syndrome

    Clinical Genetics

    Volume 76, Issue 4, October 2009, Pages: 398–403, KK Selmer, A-S Eriksson, K Brandal, T Egeland, C Tallaksen and DE Undlien

    Version of Record online : 10 AUG 2009, DOI: 10.1111/j.1399-0004.2009.01208.x

  11. You have free access to this content
    The genetics of Dravet syndrome

    Epilepsia

    Volume 52, Issue s2, April 2011, Pages: 24–29, Carla Marini, Ingrid E. Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara and Renzo Guerrini

    Version of Record online : 4 APR 2011, DOI: 10.1111/j.1528-1167.2011.02997.x

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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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    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

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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

  15. You have full text access to this OnlineOpen article
    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

  16. You have free access to this content
    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

  17. You have free access to this content
    Genetic testing in the epilepsies—Report of the ILAE Genetics Commission

    Epilepsia

    Volume 51, Issue 4, April 2010, Pages: 655–670, Ruth Ottman, Shinichi Hirose, Satish Jain, Holger Lerche, Iscia Lopes-Cendes, Jeffrey L. Noebels, José Serratosa, Federico Zara and Ingrid E. Scheffer

    Version of Record online : 19 JAN 2010, DOI: 10.1111/j.1528-1167.2009.02429.x

  18. You have free access to this content
    Dravet syndrome: Seizure control and gait in adults with different SCN1A mutations

    Epilepsia

    Volume 53, Issue 8, August 2012, Pages: 1421–1428, Jennifer J. Rilstone, Fernando M. Coelho, Berge A. Minassian and Danielle M. Andrade

    Version of Record online : 10 JUL 2012, DOI: 10.1111/j.1528-1167.2012.03583.x

  19. You have free access to this content
    Altered sleep regulation in a mouse model of SCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+)

    Epilepsia

    Volume 54, Issue 4, April 2013, Pages: 625–634, Ligia A. Papale, Christopher D. Makinson, J. Christopher Ehlen, Sergio Tufik, Michael J. Decker, Ketema N. Paul and Andrew Escayg

    Version of Record online : 11 JAN 2013, DOI: 10.1111/epi.12060

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    Acute encephalopathy in children with Dravet syndrome

    Epilepsia

    Volume 53, Issue 1, January 2012, Pages: 79–86, Akihisa Okumura, Mitsugu Uematsu, George Imataka, Manabu Tanaka, Tohru Okanishi, Tetsuo Kubota, Akira Sudo, Jun Tohyama, Megumi Tsuji, Iori Ohmori, Misako Naiki, Ayako Hiraiwa-Sofue, Hitoshi Sato, Shinji Saitoh and Toshiaki Shimizu

    Version of Record online : 16 NOV 2011, DOI: 10.1111/j.1528-1167.2011.03311.x