Works matching IS 00139580 AND DT 2006 AND VI 47 AND IP 10

Results: 36

Ethical, Legal, and Social Dimensions of Epilepsy Genetics.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1595, doi. 10.1111/j.1528-1167.2006.00632.x

By:

Shostak, Sara;
Ottman, Ruth

Publication type:

Article

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.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1700, doi. 10.1111/j.1528-1167.2006.00633.x

By:

Theodore, William H.;
Spencer, Susan S.;
Wiebe, Samuel;
Langfitt, John T.;
Ali, Amza;
Shafer, Patricia O.;
Berg, Anne T.;
Vickrey, Barbara G.

Publication type:

Article

Three Brief Epileptic Seizures Reduce Inhibitory Synaptic Currents, GABAA Currents, and GABAA-Receptor Subunits.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1655, doi. 10.1111/j.1528-1167.2006.00634.x

By:

Evans, M. Steven;
Cady, Craig J.;
Disney, Kimberly E.;
Yang, Li;
LaGuardia, James J.

Publication type:

Article

Prevalence of Epilepsy in Bursa City Center, an Urban Area of Turkey.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1691, doi. 10.1111/j.1528-1167.2006.00635.x

By:

Çalişir, Nermin;
Bora, Ibrahim;
Irgil, Emel;
Boz, Meral

Publication type:

Article

Autosomal Dominant Early-onset Cortical Myoclonus, Photic-induced Myoclonus, and Epilepsy in a Large Pedigree.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1643, doi. 10.1111/j.1528-1167.2006.00636.x

By:

Gardella, Elena;
Tinuper, Paolo;
Marini, Carla;
Guerrini, Renzo;
Parrini, Elena;
Bisulli, Francesca;
Liguori, Rocco;
Montagna, Pasquale;
Lugaresi, Elio

Publication type:

Article

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1622, doi. 10.1111/j.1528-1167.2006.00637.x

By:

Hedera, Peter;
Ma, Shaochun;
Blair, Marcia A.;
Taylor, Kelly A.;
Hamati, Aline;
Bradford, Yuki;
Abou-Khalil, Bassel;
Haines, Jonathan L.

Publication type:

Article

Altered Tryptophan Metabolism in the Brain of Cystatin B-Deficient Mice: A Model System for Progressive Myoclonus Epilepsy.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1650, doi. 10.1111/j.1528-1167.2006.00638.x

By:

Vaarmann, Annika;
Kaasik, Allen;
Zharkovsky, Alexander

Publication type:

Article

Do Children with Benign Rolandic Epilepsy Have a Higher Prevalence of Migraine than Those with Other Partial Epilepsies or Nonepilepsy Controls?

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1674, doi. 10.1111/j.1528-1167.2006.00639.x

By:

Wirrell, Elaine C.;
Hamiwka, Lorie D.

Publication type:

Article

Increased GABAA-Receptor α1-Subunit Expression in Hippocampal Dentate Gyrus after Early-life Status Epilepticus.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1665, doi. 10.1111/j.1528-1167.2006.00640.x

By:

Raol, YogendraSinh H.;
Zhang, Guojun;
Lund, Ingrid V.;
Porter, Brenda E.;
Maronski, Margaret A.;
Brooks-Kayal, Amy R.

Publication type:

Article

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1629, doi. 10.1111/j.1528-1167.2006.00641.x

By:

Mancardi, Maria Margherita;
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

Publication type:

Article

Nonfunctional SCN1A Is Common in Severe Myoclonic Epilepsy of Infancy.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1636, doi. 10.1111/j.1528-1167.2006.00643.x

By:

Ohmori, Iori;
Kahlig, Kristopher M.;
Rhodes, Thomas H.;
Wang, Dao W.;
George, Jr., Alfred L.

Publication type:

Article

Coexistence of Idiopathic Rolandic Epilepsy and CSWS in Two Families.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1723, doi. 10.1111/j.1528-1167.2006.00644.x

By:

De Tiège, Xavier;
Goldman, Serge;
Verheulpen, Denis;
Aeby, Alec;
Poznanski, Nathalie;
Van Bogaert, Patrick

Publication type:

Article

SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1732, doi. 10.1111/j.1528-1167.2006.00645.x

By:

Morimoto, Masafumi;
Mazaki, Emi;
Nishimura, Akira;
Chiyonobu, Tomohiro;
Sawai, Yasuko;
Murakami, Aki;
Nakamura, Keiko;
Inoue, Ikuyo;
Ogiwara, Ikuo;
Sugimoto, Tohru;
Yamakawa, Kazuhiro

Publication type:

Article

Exacerbation of Seizures in Medial Temporal Lobe Epilepsy Due to an α1-Adrenergic Antagonist.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1741, doi. 10.1111/j.1528-1167.2006.00646.x

By:

Iváñez, Vicente;
Ojeda, Joaquín

Publication type:

Article

Mosaic SCN1A Mutation in Familial Severe Myoclonic Epilepsy of Infancy.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1737, doi. 10.1111/j.1528-1167.2006.00675.x

By:

Marini, Carla;
Mei, Davide;
Cross, J. Helen;
Guerrini, Renzo

Publication type:

Article

Heterogeneity at the JME 6p11–12 Locus: Absence of Mutations in the EFHC1 Gene in Linked Dutch Families.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1743, doi. 10.1111/j.1528-1167.2006.00676.x

By:

Pinto, Dalila;
Louwaars, Sandrien;
Westland, Birgit;
Volkers, Linda;
de Haan, Gerrit-Jan;
Trenité, Dorothée G.A. Kasteleijn-Nolst;
Lindhout, Dick;
Koeleman, Bobby P. C.

Publication type:

Article

Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1682, doi. 10.1111/j.1528-1167.2006.00677.x

By:

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.

Publication type:

Article

Gene Profiling in Temporal Lobe Epilepsy Tissue and Dysplastic Lesions.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1608, doi. 10.1111/j.1528-1167.2006.00712.x

By:

Crino, Peter B.;
Becker, Albert J.

Publication type:

Article

Genomics of Brain and Blood: Progress and Pitfalls.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1603, doi. 10.1111/j.1528-1167.2006.00809.x

By:

Sharp, Frank R.;
Lit, Lisa;
Xu, Huichun;
Apperson, Michelle;
Walker, Wynn;
Wong, Brenda;
Gilbert, Donald L.;
Hershey, Andrew;
Glauser, Tracy A.

Publication type:

Article

Can We Increase the Likelihood of Success for Future Association Studies in Epilepsy?

Published in:

2006

By:

Durner, Martina;
Gorroochurn, Prakash;
Marini, Carla;
Guerrini, Renzo

Publication type:

Editorial

No Association of Single Nucleotide Polymorphisms in the μ-Opioid Receptor Subunit Gene with Idiopathic Generalized Epilepsy.

Published in:

Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1728, doi. 10.1111/j.1528-1167.2006.00844.x

By:

Catherine, Barratt;
Teck, Lai;
Lina, Nashef;
Antonio, Valentin;
Leonora, Fisniku;
Nicholas, Moran;
Philip, Asherson;
Andrew, Makoff

Publication type:

Article

Invited Comments on the Shostak and Ottman Review.

Published in:

2006

By:

Anderson, V. Elving

Publication type:

Letter

Response from Drs. Shostak and Ottman.

Published in:

2006

By:

Shostak, Sara;
Ottman, Ruth

Publication type:

Letter

Response to Editorial by Durner et al.

Published in:

2006

By:

Asherson, Philip;
Nashef, Lina;
Moran, Nicolas;
Makoff, Andrew

Publication type:

Letter

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2006

By:

Benson, Peter;
Kleinman, Arthur

Publication type:

Letter

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2006

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Bird, Thomas D.

Publication type:

Letter

Comment.

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2006

By:

Goldman, Alica;
Noebels, Jeffrey

Publication type:

Letter

Comment.

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2006

By:

Conrad, Peter

Publication type:

Letter

Comment.

Published in:

2006

By:

Grinton, Bronwyn E.;
Scheffer, Ingrid E.;
Berkovic, Samuel F.

Publication type:

Letter

Comment.

Published in:

2006

By:

Scambler, Graham

Publication type:

Letter

Comment.

Published in:

2006

By:

Schneider, Joseph

Publication type:

Letter

Comment.

Published in:

2006

By:

Serratosa, Jose M.

Publication type:

Letter

Works matching IS 00139580 AND DT 2006 AND VI 47 AND IP 10

Ethical, Legal, and Social Dimensions of Epilepsy Genetics.

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.

Three Brief Epileptic Seizures Reduce Inhibitory Synaptic Currents, GABA<sub>A</sub> Currents, and GABA<sub>A</sub>-Receptor Subunits.

Prevalence of Epilepsy in Bursa City Center, an Urban Area of Turkey.

Autosomal Dominant Early-onset Cortical Myoclonus, Photic-induced Myoclonus, and Epilepsy in a Large Pedigree.

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22.

Altered Tryptophan Metabolism in the Brain of Cystatin B-Deficient Mice: A Model System for Progressive Myoclonus Epilepsy.

Do Children with Benign Rolandic Epilepsy Have a Higher Prevalence of Migraine than Those with Other Partial Epilepsies or Nonepilepsy Controls?

Increased GABA<sub>A</sub>-Receptor α1-Subunit Expression in Hippocampal Dentate Gyrus after Early-life Status Epilepticus.

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations.

Nonfunctional SCN1A Is Common in Severe Myoclonic Epilepsy of Infancy.

Coexistence of Idiopathic Rolandic Epilepsy and CSWS in Two Families.

SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy.

Exacerbation of Seizures in Medial Temporal Lobe Epilepsy Due to an α<sub>1</sub>-Adrenergic Antagonist.

Mosaic SCN1A Mutation in Familial Severe Myoclonic Epilepsy of Infancy.

Heterogeneity at the JME 6p11–12 Locus: Absence of Mutations in the EFHC1 Gene in Linked Dutch Families.

Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies.

Gene Profiling in Temporal Lobe Epilepsy Tissue and Dysplastic Lesions.

Genomics of Brain and Blood: Progress and Pitfalls.

Can We Increase the Likelihood of Success for Future Association Studies in Epilepsy?

No Association of Single Nucleotide Polymorphisms in the μ-Opioid Receptor Subunit Gene with Idiopathic Generalized Epilepsy.

Invited Comments on the Shostak and Ottman Review.

Response from Drs. Shostak and Ottman.

Response to Editorial by Durner et al.

NEXT MONTH IN Epilepsia.

Online Early.

ANNOUNCEMENTS.

CALENDAR OF MEETINGS.

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