Cantitate/Preț
Produs

Genetics of Epilepsy: Progress in Brain Research, cartea 213

Ortrud Steinlein
en Limba Engleză Hardback – 2 sep 2014
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.


  • Authors are the leading experts in the field of epilepsy research
  • Book covers the most important aspects of epilepsy
  • Interesting for both scientists and clinicians
Citește tot Restrânge

Din seria Progress in Brain Research

Preț: 115197 lei

Preț vechi: 126590 lei
-9% Nou

Puncte Express: 1728

Preț estimativ în valută:
22049 22980$ 18354£

Carte tipărită la comandă

Livrare economică 28 decembrie 24 - 11 ianuarie 25

Preluare comenzi: 021 569.72.76

Specificații

ISBN-13: 9780444633262
ISBN-10: 044463326X
Pagini: 346
Ilustrații: black & white illustrations, black & white line drawings, black & white tables, figures
Dimensiuni: 191 x 235 x 23 mm
Greutate: 0.93 kg
Ediția:New.
Editura: ELSEVIER SCIENCE
Seria Progress in Brain Research


Public țintă

Neuroscientists, psychologists, neurologists. The volume will serve as an outstanding reference for both those just entering the field and experts seeking an update on this fast moving area.

Cuprins

  1. Genetic Heterogeneity in Familial Nocturnal Frontal Lobe EpilepsyOrtrud K. Steinlein
  2. Potassium Channel Genes and Benign Familial Neonatal EpilepsySnezana Maljevic and Holger Lerche
  3. Mutant GABAA Receptor Subunits in Genetic (Idiopathic) EpilepsyShinichi Hirose
  4. The Role of Calcium Channel Mutations in Human EpilepsyAntonio Gambardella and Angelo Labate
  5. Mechanisms Underlying Epilepsies Associated with Sodium Channel MutationsOrtrud K. Steinlein
  6. The Progressive Myoclonus EpilepsiesBerge A. Minassian
  7. Genetics Advances in Autosomal Dominant Focal Epilepsies: Focus on DEPDC5Stéphanie Baulac
  8. PRRT2: A Major Cause of Infantile Epilepsy and other Paroxysmal Disorders of ChildhoodCarlo Nobile and Pasquale Striano
  9. LGI1: From Zebrafish to Human EpilepsyJohn K. Cowell
  10. Morphogenesis and Timing of Genetically-Programmed Brain Malformations in Relation to EpilepsyHarvey B. Sarnat and Laura Flores-Sarnat
  11. 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 SlowDavid A. Greenberg and William L. Stewart
  12. Monogenic Models of Absence Epilepsy: Windows into the Complex Balance between Inhibition and Excitation in Thalamocortical MicrocircuitsAtul Maheshwari and Jeffrey L. Noebels
  13. New Technologies in Molecular Genetics: The Impact on Epilepsy ResearchIngo Helbig
  14. Epigenetic Mechanisms in Epilepsy Katja Kobow and Ingmar Blümcke