|
|
|
|
| LEADER |
04138nam a2200649 4500 |
| 001 |
ocn891396361 |
| 003 |
OCoLC |
| 005 |
20180501122021.0 |
| 006 |
m o d |
| 007 |
cr ||||||||||| |
| 008 |
140919s2014 enka ob 001 0 eng d |
| 040 |
|
|
|a E7B
|b eng
|e rda
|e pn
|c E7B
|d OCLCO
|d UIU
|d OCLCF
|d EBLCP
|d N$T
|d YDXCP
|d IDEBK
|d CN4UL
|d MMU
|d OCLCO
|d VT2
|d OCLCA
|d YDX
|d OCLCQ
|d TFH
|d CASUM
|d OCLCO
|d UAB
|d OCLCO
|d GrThAP
|
| 016 |
7 |
|
|a 016823566
|2 Uk
|
| 016 |
7 |
|
|a 016867816
|2 Uk
|
| 019 |
|
|
|a 890530113
|a 899277709
|a 906022475
|
| 020 |
|
|
|a 9780444633330
|q (e-book)
|
| 020 |
|
|
|a 0444633332
|q (e-book)
|
| 020 |
|
|
|a 9780444633262
|q (print)
|
| 020 |
|
|
|a 044463326X
|q (print)
|
| 035 |
|
|
|a (OCoLC)891396361
|z (OCoLC)890530113
|z (OCoLC)899277709
|z (OCoLC)906022475
|
| 050 |
|
4 |
|a RC372
|b .G46 2014eb
|
| 060 |
|
4 |
|a WL 385
|
| 072 |
|
7 |
|a HEA
|x 039000
|2 bisacsh
|
| 072 |
|
7 |
|a MED
|x 014000
|2 bisacsh
|
| 072 |
|
7 |
|a MED
|x 022000
|2 bisacsh
|
| 072 |
|
7 |
|a MED
|x 112000
|2 bisacsh
|
| 072 |
|
7 |
|a MED
|x 045000
|2 bisacsh
|
| 082 |
0 |
4 |
|a 616.853
|2 23
|
| 049 |
|
|
|a TEFA
|
| 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 / Stéphanie 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 Blümcke.
|
| 588 |
0 |
|
|a Online resource; title from resource home page (ScienceDirect, viewed November 30, 2015).
|
| 650 |
|
0 |
|a Epilepsy
|x Etiology.
|
| 650 |
|
0 |
|a Epilepsy
|x Genetic aspects.
|
| 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
|
| 650 |
1 |
2 |
|a Epilepsy
|x etiology.
|
| 650 |
1 |
2 |
|a Epilepsy
|x genetics.
|
| 655 |
|
4 |
|a Electronic books.
|
| 655 |
|
7 |
|a Electronic books.
|2 lcgft
|
| 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 Volume 213.
|x 0079-6123
|
| 856 |
4 |
0 |
|u https://www.sciencedirect.com/science/bookseries/00796123/213
|z Full Text via HEAL-Link
|
