Genetics of Epilepsy
-10%
portes grátis
Genetics of Epilepsy
Steinlein, Ortrud (Institute of Human Genetics, University Hospital Munich, Ludwig-Maximilians University, Germany)
Elsevier Science & Technology
09/2014
346
Dura
Inglês
9780444633262
15 a 20 dias
Descrição não disponível.
Genetic Heterogeneity in Familial Nocturnal Frontal Lobe Epilepsy Ortrud K. Steinlein Potassium Channel Genes and Benign Familial Neonatal Epilepsy Snezana Maljevic and Holger Lerche Mutant GABAA Receptor Subunits in Genetic (Idiopathic) Epilepsy Shinichi Hirose The Role of Calcium Channel Mutations in Human Epilepsy Antonio Gambardella and 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 Stephanie Baulac PRRT2: A Major Cause of Infantile Epilepsy and other Paroxysmal Disorders of Childhood Carlo Nobile and Pasquale Striano LGI1: From Zebrafish to Human Epilepsy John K. Cowell Morphogenesis and Timing of Genetically-Programmed Brain Malformations in Relation to Epilepsy Harvey B. Sarnat and 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 and William L. Stewart Monogenic Models of Absence Epilepsy: Windows into the Complex Balance between Inhibition and Excitation in Thalamocortical Microcircuits Atul Maheshwari and Jeffrey L. Noebels New Technologies in Molecular Genetics: The Impact on Epilepsy Research Ingo Helbig Epigenetic Mechanisms in Epilepsy Katja Kobow and Ingmar Blumcke
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Genetic Heterogeneity in Familial Nocturnal Frontal Lobe Epilepsy Ortrud K. Steinlein Potassium Channel Genes and Benign Familial Neonatal Epilepsy Snezana Maljevic and Holger Lerche Mutant GABAA Receptor Subunits in Genetic (Idiopathic) Epilepsy Shinichi Hirose The Role of Calcium Channel Mutations in Human Epilepsy Antonio Gambardella and 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 Stephanie Baulac PRRT2: A Major Cause of Infantile Epilepsy and other Paroxysmal Disorders of Childhood Carlo Nobile and Pasquale Striano LGI1: From Zebrafish to Human Epilepsy John K. Cowell Morphogenesis and Timing of Genetically-Programmed Brain Malformations in Relation to Epilepsy Harvey B. Sarnat and 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 and William L. Stewart Monogenic Models of Absence Epilepsy: Windows into the Complex Balance between Inhibition and Excitation in Thalamocortical Microcircuits Atul Maheshwari and Jeffrey L. Noebels New Technologies in Molecular Genetics: The Impact on Epilepsy Research Ingo Helbig Epigenetic Mechanisms in Epilepsy Katja Kobow and Ingmar Blumcke
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
