Epilepsia

Ethical, Legal, and Social Dimensions of Epilepsy Genetics
pp. 1595-1602(8)
Authors: Shostak, Sara; Ottman, Ruth

Genomics of Brain and Blood: Progress and Pitfalls
pp. 1603-1607(5)
Authors: Sharp, Frank R; Lit, Lisa; Xu, Huichun; Apperson, Michelle; Walker, Wynn; Wong, Brenda; Gilbert, Donald L.; Hershey, Andrew; Glauser, Tracy A.

Gene Profiling in Temporal Lobe Epilepsy Tissue and Dysplastic Lesions
pp. 1608-1616(9)
Authors: Crino, Peter B.; Becker, Albert J.

Can We Increase the Likelihood of Success for Future Association Studies in Epilepsy?
pp. 1617-1621(5)
Authors: Durner, Martina; Gorroochurn, Prakash; Marini, Carla; Guerrini, Renzo

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22
pp. 1622-1628(7)
Authors: Hedera, Peter; Ma, Shaochun; Blair, Marcia A.; Taylor, Kelly A.; Hamati, Aline; Bradford, Yuki; Abou-Khalil, Bassel; Haines, Jonathan L.

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations
pp. 1629-1635(7)
Authors: Margherita Mancardi, Maria; Striano, Pasquale; Gennaro, Elena; Madia, Francesca; Paravidino, Roberta; Scapolan, Sara; dalla Bernardina, Bernardo; Bertini, Enrico; Bianchi, Amedeo; Capovilla, Giuseppe; Darra, Francesca; Elia, Maurizio; Freri, Elena; Gobbi, Giuseppe; Granata, Tiziana; Guerrini, Renzo; Pantaleoni, Chiara; Parmeggiani, Antonia; Romeo, Antonino; Santucci, Margherita; Vecchi, Marilena; Veggiotti, Pierangelo; Vigevano, Federico; Pistorio, Angela; Gaggero, Roberto; Zara, Federico

Nonfunctional SCN1A Is Common in Severe Myoclonic Epilepsy of Infancy
pp. 1636-1642(7)
Authors: Ohmori, Iori; Kahlig, Kristopher M.; Rhodes, Thomas H.; Wang, Dao W.; George, Alfred L.

Autosomal Dominant Early-onset Cortical Myoclonus, Photic-induced Myoclonus, and Epilepsy in a Large Pedigree
pp. 1643-1649(7)
Authors: Gardella, Elena; Tinuper, Paolo; Marini, Carla; Guerrini, Renzo; Parrini, Elena; Bisulli, Francesca; Liguori, Rocco; Montagna, Pasquale; Lugaresi, Elio

Altered Tryptophan Metabolism in the Brain of Cystatin B-Deficient Mice: A Model System for Progressive Myoclonus Epilepsy
pp. 1650-1654(5)
Authors: Vaarmann, Annika; Kaasik, Allen; Zharkovsky, Alexander

Three Brief Epileptic Seizures Reduce Inhibitory Synaptic Currents, GABA_A Currents, and GABA_A-Receptor Subunits
pp. 1655-1664(10)
Authors: Evans, M. Steven; Cady, Craig J.; Disney, Kimberly E.; Yang, Li; LaGuardia, James J.

Increased GABA_A-Receptor α1-Subunit Expression in Hippocampal Dentate Gyrus after Early-life Status Epilepticus
pp. 1665-1673(9)
Authors: Raol, YogendraSinh H.; Zhang, Guojun; Lund, Ingrid V.; Porter, Brenda E.; Maronski, Margaret A.; Brooks-Kayal, Amy R.

Do Children with Benign Rolandic Epilepsy Have a Higher Prevalence of Migraine than Those with Other Partial Epilepsies or Nonepilepsy Controls?
pp. 1674-1681(8)
Authors: Wirrell, Elaine C.; Hamiwka, Lorie D.

Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies
pp. 1682-1690(9)
Authors: Hempelmann, Anne; Taylor, Kirsten P.; Heils, Armin; Lorenz, Susanne; Prud'Homme, Jean-Francois; Nabbout, Rima; Dulac, Olivier; Rudolf, Gabrielle; Zara, Federico; Bianchi, Amedeo; Robinson, Robert; Gardiner, R. Mark; Covanis, Athanasios; Lindhout, Dick; Stephani, Ulrich; Elger, Christian E.; Weber, Yvonne G.; Lerche, Holger; Nürnberg, Peter; Kron, Katherine L.; Scheffer, Ingrid E.; Mulley, John C.; Berkovic, Samuel F.; Sander, Thomas

Prevalence of Epilepsy in Bursa City Center, an Urban Area of Turkey
pp. 1691-1699(9)
Authors: Çalişir, Nermin; Bora, Ibrahim; Irgil, Emel; Boz, Meral

Epilepsy in North America: A Report Prepared under the Auspices of the Global Campaign against Epilepsy, the International Bureau for Epilepsy, the International League Against Epilepsy, and the World Health Organization
pp. 1700-1722(23)
Authors: Theodore, William H.; Spencer, Susan S.; Wiebe, Samuel; Langfitt, John T.; Ali, Amza; Shafer, Patricia O.; Berg, Anne T.; Vickrey, Barbara G.

Coexistence of Idiopathic Rolandic Epilepsy and CSWS in Two Families
pp. 1723-1727(5)
Authors: De Tiège, Xavier; Goldman, Serge; Verheulpen, Denis; Aeby, Alec; Poznanski, Nathalie; Van Bogaert, Patrick

No Association of Single Nucleotide Polymorphisms in the μ-Opioid Receptor Subunit Gene with Idiopathic Generalized Epilepsy
pp. 1728-1731(4)
Authors: Barratt, Catherine; Lai, Teck; Nashef, Lina; Valentin, Antonio; Fisniku, Leonora; Moran, Nicholas; Asherson, Philip; Makoff, Andrew

SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy
pp. 1732-1736(5)
Authors: Morimoto, Masafumi; Mazaki, Emi; Nishimura, Akira; Chiyonobu, Tomohiro; Sawai, Yasuko; Murakami, Aki; Nakamura, Keiko; Inoue, Ikuyo; Ogiwara, Ikuo; Sugimoto, Tohru; Yamakawa, Kazuhiro

Mosaic SCN1A Mutation in Familial Severe Myoclonic Epilepsy of Infancy
pp. 1737-1740(4)
Authors: Marini, Carla; Mei, Davide; Helen Cross, J.; Guerrini, Renzo

Exacerbation of Seizures in Medial Temporal Lobe Epilepsy Due to an α₁-Adrenergic Antagonist
pp. 1741-1742(2)
Authors: Iváñez, Vicente; Ojeda, Joaquín

Heterogeneity at the JME 6p11-12 Locus: Absence of Mutations in the EFHC1 Gene in Linked Dutch Families
pp. 1743-1746(4)
Authors: Pinto, Dalila; Louwaars, Sandrien; Westland, Birgit; Volkers, Linda; de Haan, Gerrit-Jan; Trenité, Dorothée G.A. Kasteleijn-Nolst; Lindhout, Dick; Koeleman, Bobby P.C.

Invited Comments on the Shostak and Ottman Review
pp. 1747-1747(1)

Comment
pp. 1747-1748(2)

Comment
pp. 1748-1749(2)

Comment
pp. 1749-1750(2)

Comment
pp. 1750-1751(2)

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pp. 1751-1752(2)

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pp. 1752-1753(2)

Comment
pp. 1753-1754(2)

Comment
pp. 1754-1755(2)

Response from Drs. Shostak and Ottman
pp. 1755-1756(2)

Response to Editorial by Durner et al.
pp. 1757-1758(2)

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pp. 1758-1758(1)

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pp. 1758-1758(1)

ANNOUNCEMENTS
pp. 1758-1759(2)

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pp. 1760-1760(1)