Genetics of epilepsy /

Λεπτομέρειες βιβλιογραφικής εγγραφής
Άλλοι συγγραφείς: Steinlein, Ortrud K. (Επιμελητής έκδοσης)
Μορφή: Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Amsterdam, the Netherlands : Elsevier, 2014.
Έκδοση:First edition.
Σειρά:Progress in brain research ; Volume 213.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
Πίνακας περιεχομένων:
  • 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.