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
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
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
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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Published in:
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Publication type:
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Published in:
2006
Publication type:
Other
ANNOUNCEMENTS.
Published in:
2006
Publication type:
Other
CALENDAR OF MEETINGS.
Published in:
2006
Publication type:
Other
Comment.
Published in:
2006
By:
- Benson, Peter;
- Kleinman, Arthur
Publication type:
Letter
Comment.
Published in:
2006
By:
- Bird, Thomas D.
Publication type:
Letter
Comment.
Published in:
2006
By:
- Conrad, Peter
Publication type:
Letter
Comment.
Published in:
2006
By:
- Goldman, Alica;
- Noebels, Jeffrey
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.

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

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

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.

Comment.

Comment.

Comment.

Comment.

Comment.

Comment.

Comment.

Comment.