Works matching IS 00139580 AND DT 2012 AND VI 53


Results: 412
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    Epigenetics and epilepsy.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, p. 2, doi. 10.1111/epi.12030
    By:
    • Roopra, Avtar;
    • Dingledine, Raymond;
    • Hsieh, Jenny
    Publication type:
    Article
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    Introduction.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, p. 1, doi. 10.1111/epi.12023
    By:
    • Bialer, Meir;
    • Smith, Phil E. M.
    Publication type:
    Article
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    Introduction.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, p. 1, doi. 10.1111/j.1528-1167.2012.03708.x
    By:
    • Smith, Phil;
    • Bialer, Meir
    Publication type:
    Article
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    The parasomnias: Mechanisms and treatment.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, p. 12, doi. 10.1111/j.1528-1167.2012.03710.x
    By:
    • Tinuper, Paolo;
    • Bisulli, Francesca;
    • Provini, Federica
    Publication type:
    Article
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    Cardiac syncope.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, p. 34, doi. 10.1111/j.1528-1167.2012.03713.x
    By:
    • Anderson, Joseph;
    • O'Callaghan, Peter
    Publication type:
    Article
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    Emil Theodor Kocher-Valve surgery for epilepsy.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2099, doi. 10.1111/j.1528-1167.2012.03663.x
    By:
    • Surbeck, Werner;
    • Stienen, Martin Nikolaus;
    • Hildebrandt, Gerhard
    Publication type:
    Article
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    Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2111, doi. 10.1111/j.1528-1167.2012.03649.x
    By:
    • Marini, Carla;
    • Darra, Francesca;
    • Specchio, Nicola;
    • Mei, Davide;
    • Terracciano, Alessandra;
    • Parmeggiani, Lucio;
    • Ferrari, Annarita;
    • Sicca, Federico;
    • Mastrangelo, Massimo;
    • Spaccini, Luigina;
    • Canopoli, Maria Lucia;
    • Cesaroni, Elisabetta;
    • Zamponi, Nelia;
    • Caffi, Lorella;
    • Ricciardelli, Paolo;
    • Grosso, Salvatore;
    • Pisano, Tiziana;
    • Canevini, Maria Paola;
    • Granata, Tiziana;
    • Accorsi, Patrizia
    Publication type:
    Article
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    Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, n. 12, p. e204, doi. 10.1111/epi.12007
    By:
    • Arsov, Todor;
    • Mullen, Saul A.;
    • Damiano, John A.;
    • Lawrence, Kate M.;
    • Huh, Linda L.;
    • Nolan, Melinda;
    • Young, Helen;
    • Thouin, Anaïs;
    • Dahl, Hans-Henrik M.;
    • Berkovic, Samuel F.;
    • Crompton, Douglas E.;
    • Sadleir, Lynette G.;
    • Scheffer, Ingrid E.
    Publication type:
    Article
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    Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2120, doi. 10.1111/j.1528-1167.2012.03718.x
    By:
    • Canafoglia, Laura;
    • Gennaro, Elena;
    • Capovilla, Giuseppe;
    • Gobbi, Giuseppe;
    • Boni, Antonella;
    • Beccaria, Francesca;
    • Viri, Maurizio;
    • Michelucci, Roberto;
    • Agazzi, Pamela;
    • Assereto, Stefania;
    • Coviello, Domenico A.;
    • Di Stefano, Maria;
    • Rossi Sebastiano, Davide;
    • Franceschetti, Silvana;
    • Zara, Federico
    Publication type:
    Article
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    Neurocognitive profiles in children with epilepsy.

    Published in:
    Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2156, doi. 10.1111/j.1528-1167.2012.03706.x
    By:
    • Kernan, Claudia L.;
    • Asarnow, Robert;
    • Siddarth, Prabha;
    • Gurbani, Suresh;
    • Lanphier, Erin K.;
    • Sankar, Raman;
    • Caplan, Rochelle
    Publication type:
    Article
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    Thank you.

    Published in:
    2012
    By:
    • Schwartzkroin, Philip A.;
    • Shorvon, Simon D.
    Publication type:
    Editorial
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