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Genetics of epilepsy /
The book chapters cover different aspects of epilepsy genetics, starting with the ""classical"" concept of epilepsies as ion channel disorders. The second part of the book gives credit to the fact that by now non-ion channel genes are recognized as equally important causes of epi...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Amsterdam, the Netherlands :
Elsevier,
2014.
|
| Edición: | First edition. |
| Colección: | Progress in brain research ;
v. 213. |
| Temas: | |
| Acceso en línea: | Texto completo Texto completo |
MARC
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| 245 | 0 | 0 | |a Genetics of epilepsy / |c edited by Ortrud K. Steinlein. |
| 250 | |a First edition. | ||
| 264 | 1 | |a Amsterdam, the Netherlands : |b Elsevier, |c 2014. | |
| 300 | |a 1 online resource (vii, 329 pages) : |b color illustrations | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Progress in Brain Research, |x 0079-6123 ; |v volume 213 | |
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 0 | |a Genetic heterogeneity in familial nocturnal frontal lobe epilepsy / ortrud K. Steinlein -- Potassium channel genes and benign familial neonatal epilepsy / Snezana Maljevic, Holger Lerche -- Mutant GABA receptor subunits in genetic (idiopathic) epilepsy / Shinichi Hirose -- The role of calcium channel mutations in human epilepsy / Antonio Gambardella, Angelo Labate -- Mechanisms underlying epilepsies associated with sodium channel mutations / Ortrud K. Steinlein -- The progressive myoclonus epilepsies / Berge A. Minassian -- Genetics advances in autosomal dominant focal epilepsies : focus on DEPDC5 / St�ephanie Baulac -- PRRT2 : a major cause of infantile epilepsy and other paroxysmal disorders of childhood / Carlo Nobile, Pasquale Striano -- LGI1 : from zebrafish to human epilepsy / John K. Cowell -- Morphogenesis timing of genetically programmed brain malformations in relation to epilepsy / Harvey B. Sarnat, Laura Flores-Sarnat -- Remind me again what disease we are studying? A population genetics, genetic analysis, and real data perspective on why progress on identifying genetic influences on common epilepsies has been so slow / David A. Greenberg, William L. Stewart -- Monogenic models of absence epilepsy : windows into the complex balance between inhibition and excitation in thalamocortical microcircuits / Atul Maheshwan, Jeffrey L. Noebels -- New technologies in molecular genetics : the impact on epilepsy research / Ingo Helbig -- Epigenetic mechanisms in epilepsy / Katja Kobow, Ingmar Bl�umcke. | |
| 588 | 0 | |a Online resource; title from resource home page (ScienceDirect, viewed November 30, 2015). | |
| 520 | |a The book chapters cover different aspects of epilepsy genetics, starting with the ""classical"" concept of epilepsies as ion channel disorders. The second part of the book gives credit to the fact that by now non-ion channel genes are recognized as equally important causes of epilepsy. The concluding chapters are designed to offer the reader insight into current methods in epilepsy research. Each chapter is self-contained and deals with a selected topic of interest. <ul><li>Authors are the leading experts in the field of epilepsy research</li><li>Book covers the most important aspects | ||
| 650 | 0 | |a Epilepsy |x Etiology. | |
| 650 | 0 | |a Epilepsy |x Genetic aspects. | |
| 650 | 1 | 2 | |a Epilepsy |x genetics |0 (DNLM)D004827Q000235 |
| 650 | 2 | 2 | |a Epilepsy |x etiology |0 (DNLM)D004827Q000209 |
| 650 | 7 | |a HEALTH & FITNESS |x Diseases |x General. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Clinical Medicine. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Diseases. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Evidence-Based Medicine. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Internal Medicine. |2 bisacsh | |
| 650 | 7 | |a Epilepsy |x Etiology. |2 fast |0 (OCoLC)fst00914190 | |
| 650 | 7 | |a Epilepsy |x Genetic aspects. |2 fast |0 (OCoLC)fst00914191 | |
| 655 | 4 | |a Internet Resources. | |
| 700 | 1 | |a Steinlein, Ortrud K., |e editor. | |
| 776 | 0 | 8 | |i Print version: |t Genetics of epilepsy. |b First edition. |d Amsterdam : Elsevier, 2014 |z 9780444633262 |w (OCoLC)881022256 |
| 830 | 0 | |a Progress in brain research ; |v v. 213. |x 0079-6123 | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780444633262 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/00796123/213 |z Texto completo |