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Epilepsia

Cover image for Vol. 53 Issue 12

December 2012

Volume 53, Issue 12

Pages 2055–2209, e196–e214

  1. FROM THE EDITORS

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. You have free access to this content
      Thank you (pages 2055–2056)

      Philip A. Schwartzkroin and Simon D. Shorvon

      Version of Record online: 3 DEC 2012 | DOI: 10.1111/epi.12015

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  2. CRITICAL REVIEW AND INVITED COMMENTARY

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. You have free access to this content
      Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene–related encephalopathies (pages 2067–2078)

      Renzo Guerrini and Elena Parrini

      Version of Record online: 21 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03656.x

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      The prognosis of idiopathic generalized epilepsy (pages 2079–2090)

      Udaya Seneviratne, Mark Cook and Wendyl D’Souza

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/j.1528-1167.2012.03723.x

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      Frontal lobe function and structure in juvenile myoclonic epilepsy: A comprehensive review of neuropsychological and imaging data (pages 2091–2098)

      Britta Wandschneider, Pamela J. Thompson, Christian Vollmar and Matthias J. Koepp

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/epi.12003

  3. HISTORICAL REVIEW

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. You have free access to this content
      Emil Theodor Kocher—Valve surgery for epilepsy (pages 2099–2103)

      Werner Surbeck, Martin Nikolaus Stienen and Gerhard Hildebrandt

      Version of Record online: 11 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03663.x

  4. FULL-LENGTH ORIGINAL RESEARCH

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. You have free access to this content
      Alteration of global workspace during loss of consciousness: A study of parietal seizures (pages 2104–2110)

      Isabelle Lambert, Marie Arthuis, Aileen McGonigal, Fabrice Wendling and Fabrice Bartolomei

      Version of Record online: 27 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03690.x

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      Focal seizures with affective symptoms are a major feature of PCDH19 gene–related epilepsy (pages 2111–2119)

      Carla Marini, Francesca Darra, Nicola Specchio, Davide Mei, Alessandra Terracciano, Lucio Parmeggiani, Annarita Ferrari, Federico Sicca, Massimo Mastrangelo, Luigina Spaccini, Maria Lucia Canopoli, Elisabetta Cesaroni, Nelia Zamponi, Lorella Caffi, Paolo Ricciardelli, Salvatore Grosso, Tiziana Pisano, Maria Paola Canevini, Tiziana Granata, Patrizia Accorsi, Domenica Battaglia, Raffaella Cusmai, Federico Vigevano, Bernardo Dalla Bernardina and Renzo Guerrini

      Version of Record online: 4 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03649.x

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      Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations (pages 2120–2127)

      Laura Canafoglia, Elena Gennaro, Giuseppe Capovilla, Giuseppe Gobbi, Antonella Boni, Francesca Beccaria, Maurizio Viri, Roberto Michelucci, Pamela Agazzi, Stefania Assereto, Domenico A. Coviello, Maria Di Stefano, Davide Rossi Sebastiano, Silvana Franceschetti and Federico Zara

      Version of Record online: 12 OCT 2012 | DOI: 10.1111/j.1528-1167.2012.03718.x

      Corrected by:

      Erratum: Erratum

      Vol. 54, Issue 7, 1333, Version of Record online: 1 JUL 2013

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      Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy (pages 2128–2134)

      Barbara Goeggel Simonetti, Claudine Rieubland, Carolina Courage, Susi Strozzi, Sibylle Tschumi, Sabina Gallati and Johannes R. Lemke

      Version of Record online: 27 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03676.x

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      Accelerated long-term forgetting in children with idiopathic generalized epilepsy (pages 2135–2140)

      Michael B. Gascoigne, Belinda Barton, Richard Webster, Deepak Gill, Jayne Antony and Suncica Sunny Lah

      Version of Record online: 12 OCT 2012 | DOI: 10.1111/j.1528-1167.2012.03719.x

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      Family studies of individuals with eyelid myoclonia with absences (pages 2141–2148)

      Lynette G. Sadleir, Danya Vears, Brigid Regan, Natalie Redshaw, Andrew Bleasel and Ingrid E. Scheffer

      Version of Record online: 3 DEC 2012 | DOI: 10.1111/j.1528-1167.2012.03692.x

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      Association between sociodemographic status and antiepileptic drug prescriptions in children with epilepsy (pages 2149–2155)

      Peter Mattsson, Torbjörn Tomson, Karin Edebol Eeg-Olofsson, Lars Brännström and Gunilla Ringbäck Weitoft

      Version of Record online: 12 OCT 2012 | DOI: 10.1111/j.1528-1167.2012.03717.x

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      Neurocognitive profiles in children with epilepsy (pages 2156–2163)

      Claudia L. Kernan, Robert Asarnow, Prabha Siddarth, Suresh Gurbani, Erin K. Lanphier, Raman Sankar and Rochelle Caplan

      Version of Record online: 5 NOV 2012 | DOI: 10.1111/j.1528-1167.2012.03706.x

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      Epilepsy-related mortality is low in children: A 30-year population-based study in Olmsted County, MN (pages 2164–2171)

      Katherine C. Nickels, Brandon R. Grossardt and Elaine C. Wirrell

      Version of Record online: 18 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03661.x

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      Bone mineral density in a population of children and adolescents with cerebral palsy and mental retardation with or without epilepsy (pages 2172–2177)

      Giangennaro Coppola, Delia Fortunato, Ciro Mainolfi, Francesco Porcaro, Davide Roccaro, Giuseppe Signoriello, Francesca Felicia Operto and Alberto Verrotti

      Version of Record online: 7 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03639.x

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      Critical determinants of the epilepsy treatment gap: A cross-national analysis in resource-limited settings (pages 2178–2185)

      Ana-Claire L. Meyer, Tarun Dua, W. John Boscardin, José J. Escarce, Shekhar Saxena and Gretchen L. Birbeck

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/epi.12002

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      Geographic variation of epilepsy for older Americans: How close to the geographic variation of stroke? (pages 2186–2193)

      Maria Pisu, Polly Kratt, Edward Faught, Roy C. Martin, Yongin Kim, Kay Clements, Robert Knowlton, Ellen Funkhouser and Joshua S. Richman

      Version of Record online: 7 SEP 2012 | DOI: 10.1111/j.1528-1167.2012.03640.x

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      Prevalence of neurocysticercosis among people with epilepsy in rural areas of Burkina Faso (pages 2194–2202)

      Athanase Millogo, Pascal Nitiéma, Hélène Carabin, Marie Paule Boncoeur-Martel, Vedantam Rajshekhar, Zékiba Tarnagda, Nicolas Praet, Pierre Dorny, Linda Cowan, Rasmané Ganaba, Sennen Hounton, Pierre-Marie Preux and Rabiou Cissé

      Version of Record online: 13 NOV 2012 | DOI: 10.1111/j.1528-1167.2012.03687.x

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      Association between epilepsy and cysticercosis and toxocariasis: A population-based case–control study in a slum in India (pages 2203–2208)

      Gagandeep Singh, Jasleena Bawa, Deepinder Chinna, Anurag Chaudhary, Kavita Saggar, Manish Modi and Josemir W. Sander

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/epi.12005

  5. BRIEF COMMUNICATION

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. You have free access to this content
      Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences (pages e196–e199)

      Angelo Labate, Patrizia Tarantino, Maurizio Viri, Laura Mumoli, Monica Gagliardi, Antonino Romeo, Federico Zara, Grazia Annesi and Antonio Gambardella

      Version of Record online: 5 NOV 2012 | DOI: 10.1111/epi.12009

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      A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome (pages e200–e203)

      Ikuo Ogiwara, Tojo Nakayama, Tetsushi Yamagata, Hideyuki Ohtani, Emi Mazaki, Shigeru Tsuchiya, Yushi Inoue and Kazuhiro Yamakawa

      Version of Record online: 13 NOV 2012 | DOI: 10.1111/epi.12040

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      Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency (pages e204–e207)

      Todor Arsov, Saul A. Mullen, John A. Damiano, Kate M. Lawrence, Linda L. Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans-Henrik M. Dahl, Samuel F. Berkovic, Douglas E. Crompton, Lynette G. Sadleir and Ingrid E. Scheffer

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/epi.12007

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      Periictal cerebral tissue hypoxemia: A potential marker of SUDEP risk (pages e208–e211)

      Brian D. Moseley, Jeffrey W. Britton, Cindy Nelson, Ricky W. Lee and Elson So

      Version of Record online: 12 OCT 2012 | DOI: 10.1111/j.1528-1167.2012.03707.x

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      Mortality by clinical characteristics in a tertiary care cohort of adult patients with chronic epilepsy (pages e212–e214)

      Olli Nevalainen, Anssi Auvinen, Hanna Ansakorpi, Miia Artama, Jani Raitanen and Jouko Isojärvi

      Version of Record online: 25 OCT 2012 | DOI: 10.1111/epi.12006

  6. GRAY MATTERS

    1. Top of page
    2. FROM THE EDITORS
    3. CRITICAL REVIEW AND INVITED COMMENTARY
    4. HISTORICAL REVIEW
    5. FULL-LENGTH ORIGINAL RESEARCH
    6. BRIEF COMMUNICATION
    7. GRAY MATTERS
    1. Announcements

      You have free access to this content
      Announcements (page 2209)

      Version of Record online: 3 DEC 2012 | DOI: 10.1111/epi.12080

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