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Epilepsia

Cover image for Vol. 51 Issue 9

September 2010

Volume 51, Issue 9

Pages 1649–1932

  1. FROM THE EDITORS

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
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      From the Editors (page 1649)

      Philip A. Schwartzkroin and Simon D. Shorvon

      Version of Record online: 2 SEP 2010 | DOI: 10.1111/j.1528-1167.2010.02745.x

  2. CRITICAL REVIEW AND INVITED COMMENTARY

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      Sodium channel SCN1A and epilepsy: Mutations and mechanisms (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

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  3. FULL-LENGTH ORIGINAL RESEARCH

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Nav1.1 (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

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      Frameshift mutations of the ARX gene in familial Ohtahara syndrome (pages 1679–1684)

      Mitushiro Kato, Norihisa Koyama, Masayasu Ohta, Kiyokuni Miura and Kiyoshi Hayasaka

      Version of Record online: 2 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02559.x

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      Evaluation of depression risk in LGI1 mutation carriers (pages 1685–1690)

      Gary A. Heiman, Kay Kamberakis, Richard Gill, Sergey Kalachikov, Timothy A. Pedley, W. Allen Hauser and Ruth Ottman

      Version of Record online: 26 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02677.x

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      Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease (pages 1691–1698)

      Gaetan Lesca, Nadia Boutry-Kryza, Bertrand De Toffol, Mathieu Milh, Dominique Steschenko, Martine Lemesle-Martin, Louis Maillard, Giovanni Foletti, Gabrielle Rudolf, Jørgen Erik Nielsen, Bjarke á Rogvi-Hansen, Jesper Erdal, Josette Mancini, Christel Thauvin-Robinet, Amel M’Rrabet, Dorothée Ville, Pierre Szepetowski, Emmanuel Raffo, Edouard Hirsch, Philippe Ryvlin, Alain Calender and Pierre Genton

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02692.x

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      Alteration of dopamine D2/D3 receptor binding in patients with juvenile myoclonic epilepsy (pages 1699–1706)

      Christian Landvogt, Hans-Georg Buchholz, Viviane Bernedo, Mathias Schreckenberger and Konrad J. Werhahn

      Version of Record online: 8 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02569.x

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      Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice (pages 1707–1713)

      Mikhail Inyushin, Lilia Y. Kucheryavykh, Yuriy V. Kucheryavykh, Colin G. Nichols, Russell J. Buono, Thomas N. Ferraro, Serguei N. Skatchkov and Misty J. Eaton

      Version of Record online: 28 MAY 2010 | DOI: 10.1111/j.1528-1167.2010.02592.x

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      Region-specific changes in gene expression in rat brain after chronic treatment with levetiracetam or phenytoin (pages 1714–1720)

      Bjørnar Hassel, Erik Taubøll, Renee Shaw, Leif Gjerstad and Ray Dingledine

      Version of Record online: 19 MAR 2010 | DOI: 10.1111/j.1528-1167.2010.02545.x

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      Continuous local intrahippocampal delivery of adenosine reduces seizure frequency in rats with spontaneous seizures (pages 1721–1728)

      Annelies Van Dycke, Robrecht Raedt, Ine Dauwe, Tom Sante, Tine Wyckhuys, Alfred Meurs, Kristl Vonck, Wytse Wadman and Paul Boon

      Version of Record online: 17 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02700.x

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      Extrafocal threshold reductions in amygdala-kindled rats (pages 1729–1735)

      Brian W. Scott, Harrison Park, Hua Han, Ahsanullah Wahidie and W. McIntyre Burnham

      Version of Record online: 26 FEB 2010 | DOI: 10.1111/j.1528-1167.2010.02524.x

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      Susceptibility of brainstem to kindling and transfer to the forebrain (pages 1736–1744)

      Ann Lam, Naomi Whelan and Michael E. Corcoran

      Version of Record online: 2 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02551.x

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      Low frequency stimulation decreases seizure activity in a mutation model of epilepsy (pages 1745–1753)

      Kara Buehrer Kile, Nan Tian and Dominique M. Durand

      Version of Record online: 26 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02679.x

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      Alteration of NMDA receptor–mediated synaptic interactions in the lateral amygdala associated with seizure activity in a mouse model of chronic temporal lobe epilepsy (pages 1754–1762)

      Stéphanie Graebenitz, Jörg Lesting, Ludmila Sosulina, Thomas Seidenbecher and Hans-Christian Pape

      Version of Record online: 2 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02561.x

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      Evaluation of the innate and adaptive immunity in type I and type II focal cortical dysplasias (pages 1763–1773)

      Anand Iyer, Emanuele Zurolo, Wim G.M. Spliet, Peter C. Van Rijen, Johannes C. Baayen, Jan A. Gorter and Eleonora Aronica

      Version of Record online: 23 MAR 2010 | DOI: 10.1111/j.1528-1167.2010.02547.x

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      How common is brain atrophy in patients with medial temporal lobe epilepsy? (pages 1774–1779)

      Leonardo Bonilha, Jordan J. Elm, Jonathan C. Edwards, Paul S. Morgan, Christian Hicks, Carl Lozar, Zoran Rumboldt, Donna R. Roberts, Chris Rorden and Mark A. Eckert

      Version of Record online: 20 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02576.x

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      Imaging of P-glycoprotein–mediated pharmacoresistance in the hippocampus: Proof-of-concept in a chronic rat model of temporal lobe epilepsy (pages 1780–1790)

      Hero Bartmann, Christina Fuest, Christian La Fougere, Guoming Xiong, Theresa Just, Juli Schlichtiger, Petra Winter, Guido Böning, Björn Wängler, Anton Pekcec, Jonna Soerensen, Peter Bartenstein, Paul Cumming and Heidrun Potschka

      Version of Record online: 14 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02671.x

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      Induction of sodium channel Nax (SCN7A) expression in rat and human hippocampus in temporal lobe epilepsy (pages 1791–1800)

      Jan A. Gorter, Emanuele Zurolo, Anand Iyer, Kees Fluiter, Erwin A. Van Vliet, Johannes C. Baayen and Eleonora Aronica

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02678.x

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      Reliability of patterns of hippocampal sclerosis as predictors of postsurgical outcome (pages 1801–1808)

      Maria Thom, Ioannis Liagkouras, Kathryn J. Elliot, Lillian Martinian, William Harkness, Andrew McEvoy, Luis O Caboclo and Sanjay M. Sisodiya

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02681.x

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      Role of cortical dysplasia in epileptogenesis following prolonged febrile seizure (pages 1809–1819)

      Kyung-Il Park, Kon Chu, Keun-Hwa Jung, Jin-Hee Kim, Kyung-Muk Kang, Soon-Tae Lee, Hee-Kwon Park, Manho Kim, Sang Kun Lee and Jae-Kyu Roh

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02676.x

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      Utility of 3-T FLAIR and 3D short tau inversion recovery MR imaging in the preoperative diagnosis of hippocampal sclerosis: Direct comparison with 1.5-T FLAIR MR imaging (pages 1820–1828)

      Kimiaki Hashiguchi, Takato Morioka, Nobuya Murakami, Satoshi O. Suzuki, Akio Hiwatashi, Takashi Yoshiura and Tomio Sasaki

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02685.x

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      BOLD signal changes preceding negative responses in EEG-fMRI in patients with focal epilepsy (pages 1837–1845)

      Rahul Rathakrishnan, Friederike Moeller, Pierre Levan, Francois Dubeau and Jean Gotman

      Version of Record online: 7 JUN 2010 | DOI: 10.1111/j.1528-1167.2010.02643.x

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      Magnetoencephalographic correlates of different types of aura in temporal lobe epilepsy (pages 1846–1851)

      Kenjiro Fukao, Yushi Inoue and Kazuichi Yagi

      Version of Record online: 1 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02655.x

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      Increased frequency of arousal parasomnias in families with nocturnal frontal lobe epilepsy: A common mechanism? (pages 1852–1860)

      Francesca Bisulli, Luca Vignatelli, Ilaria Naldi, Laura Licchetta, Federica Provini, Giuseppe Plazzi, Lidia Di Vito, Simona Ferioli, Pasquale Montagna and Paolo Tinuper

      Version of Record online: 30 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02581.x

  4. BRIEF COMMUNICATION

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      Therapeutic time window of low-frequency stimulation at entorhinal cortex for amygdaloid-kindling seizures in rats (pages 1861–1864)

      Zheng-Hao Xu, Deng-Chang Wu, Qi Fang, Kai Zhong, Shuang Wang, Hong-Liu Sun, Shi-Hong Zhang and Zhong Chen

      Version of Record online: 16 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02663.x

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      Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3 (pages 1865–1869)

      Sarah E. Heron, Ingrid E. Scheffer, Bronwyn E. Grinton, Helen Eyre, Karen L. Oliver, Sharon Bain, Samuel F. Berkovic and John C. Mulley

      Version of Record online: 2 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02558.x

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      Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region (pages 1870–1873)

      Constanze Reutlinger, Ingo Helbig, Barbara Gawelczyk, Jose Ignacio Martin Subero, Holger Tönnies, Hiltrud Muhle, Katrin Finsterwalder, Sascha Vermeer, Rolph Pfundt, Jürgen Sperner, Irina Stefanova, Gabriele Gillessen-Kaesbach, Sarah Von Spiczak, Andreas Van Baalen, Rainer Boor, Reiner Siebert, Ulrich Stephani and Almuth Caliebe

      Version of Record online: 2 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02555.x

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      Genetic risk perception and reproductive decision making among people with epilepsy (pages 1874–1877)

      Katherine L. Helbig, Barbara A. Bernhardt, Laura J. Conway, Kathleen D. Valverde, Ingo Helbig and Michael R. Sperling

      Version of Record online: 12 FEB 2010 | DOI: 10.1111/j.1528-1167.2009.02507.x

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      Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy (pages 1878–1881)

      Chunbo Zhang, Virgina Wong, Ping Wing Ng, Colin Hiu Tung Lui, Ngai Chuen Sin, Ka Sing Wong, Larry Baum and Patrick Kwan

      Version of Record online: 30 APR 2010 | DOI: 10.1111/j.1528-1167.2010.02587.x

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      Predisposition to epilepsy—Does the ABCB1 gene play a role? (pages 1882–1885)

      Laila Nurmohamed, Facundo Garcia-Bournissen, Russell J. Buono, Michael W. Shannon and Yaron Finkelstein

      Version of Record online: 14 MAY 2010 | DOI: 10.1111/j.1528-1167.2010.02588.x

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      Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report (pages 1886–1888)

      Masaru Takayanagi, Kazuhiro Haginoya, Naoki Umehara, Taro Kitamura, Yurika Numata, Keisuke Wakusawa, Naomi Hino-Fukuyo, Emi Mazaki, Kazuhiro Yamakawa, Toshihiro Ohura and Masatoshi Ohtake

      Version of Record online: 14 MAY 2010 | DOI: 10.1111/j.1528-1167.2010.02600.x

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      Familial form of typical childhood absence epilepsy in a consanguineous context (pages 1889–1893)

      Hanen Abouda, Yosr Hizem, Amina Gargouri, Christel Depienne, Delphine Bouteiller, Florence Riant, Elisabeth Tournier-Lasserve, Isabelle Gourfinkel-An, Eric LeGuern and Riadh Gouider

      Version of Record online: 18 JUN 2010 | DOI: 10.1111/j.1528-1167.2010.02649.x

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      Screening of GABRB3 in French-Canadian families with idiopathic generalized epilepsy (pages 1894–1897)

      Pamela Lachance-Touchette, Caroline Martin, Chantal Poulin, Micheline Gravel, Lionel Carmant and Patrick Cossette

      Version of Record online: 7 JUN 2010 | DOI: 10.1111/j.1528-1167.2010.02642.x

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      Autoantibodies to glutamic acid decarboxylase in patients with epilepsy are associated with low cortical GABA levels (pages 1898–1901)

      Charlotte J. Stagg, Bethan Lang, Jonathan G. Best, Karen McKnight, Ana Cavey, Heidi Johansen-Berg, Angela Vincent and Jacqueline Palace

      Version of Record online: 7 JUN 2010 | DOI: 10.1111/j.1528-1167.2010.02644.x

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      Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria (pages 1902–1905)

      Kate M. Lawrence, Davide Mei, Mark R. Newton, Richard J. Leventer, Renzo Guerrini and Samuel F. Berkovic

      Version of Record online: 17 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02694.x

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      Clinical features of seizures associated with parahippocampal/inferior temporal lesions compared to those with hippocampal sclerosis (pages 1906–1909)

      Laura Mirandola, Radwa A. Badawy, Ann M. Saunders, Anne McIntosh, Samuel F. Berkovic and Graeme D. Jackson

      Version of Record online: 19 MAR 2010 | DOI: 10.1111/j.1528-1167.2010.02537.x

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      Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12 (pages 1910–1914)

      José Morales-Corraliza, Pilar Gómez-Garre, Raúl Sanz, Fernando Díaz-Otero, Eva Gutiérrez-Delicado and José M. Serratosa

      Version of Record online: 26 JUL 2010 | DOI: 10.1111/j.1528-1167.2010.02680.x

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      A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation (pages 1915–1918)

      François Le Gal, Christian M. Korff, Christine Monso-Hinard, Michael T. Mund, Michael Morris, Alain Malafosse and Thomas Schmitt-Mechelke

      Version of Record online: 5 AUG 2010 | DOI: 10.1111/j.1528-1167.2010.02691.x

  5. Gray Matters

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      The EpiNet project—Invitation to participate in investigator-led clinical research (pages 1919–1920)

      Peter Bergin, Ettore Beghi and John Egbuji

      Version of Record online: 2 SEP 2010 | DOI: 10.1111/j.1528-1167.2010.02647.x

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      Announcements (pages 1920–1921)

      Version of Record online: 2 SEP 2010 | DOI: 10.1111/j.1528-1167.2010.02743.x

  6. Erratum

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      Erratum (page 1922)

      Version of Record online: 2 SEP 2010 | DOI: 10.1111/j.1528-1167.2010.02744.x

      This article corrects:
  7. Instructions for Authors

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. FULL-LENGTH ORIGINAL RESEARCH
    5. BRIEF COMMUNICATION
    6. Gray Matters
    7. Erratum
    8. Instructions for Authors
    1. You have free access to this content
      Instructions for Authors (pages 1923–1932)

      Version of Record online: 2 SEP 2010 | DOI: 10.1111/j.1528-1167.2010.02749.x

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