Myoclonic Epilepsies

INTRODUCTION TO CONCEPTS AND CLASSIFICATIONS OF MYOCLONIC EPILEPSIES

History and Classification of Myoclonic Epilepsies:: From Seizures to Syndromes to Diseases

Ontogeny of the Reticular Formation:: Its Possible Relation to the Myoclonic Epilepsies

Pathophysiology of Myoclonic Epilepsies

Progressive Myoclonus Epilepsies:: EPM1, EPM2A, EPM2B

Myoclonic Status in Non-Progressive Encephalopathies

MYOCLONIC EPILEPSIES OF INFANCY AND CHILDHOOD

Severe Myoclonic Epilepsy in Infancy:: Dravets Syndrome

Severe Myoclonic Epilepsy in Infancy:: Clinical Analysis and Relation to SCN1A Mutations in a Japanese Cohort

Myoclonic Seizures in the Context of Generalized Epilepsy with Febrile Seizures Plus (GEFS+)

Benign Myoclonic Epilepsy in Infancy

Autosomal Recessive Benign Myoclonic Epilepsy of Infancy

Myoclonic Astatic Epilepsy of Early Childhood—Definition, Course, Nosography, Genetics

Idiopathic Myoclonic-Astatic Epilepsy of Early Childhood—Nosology Based on Electrophysiological and Long-Term Follow-Up Study of Patients

Myoclonic Absences:: The Seizure and the Syndrome

Eyelid Myoclonia and Absence

Childhood Absence Epilepsy Evolving to Juvenile Myoclonic Epilepsy:: Electroclinical and Genetic Features

Photosensitivity:: Genetics and Clinical Significance

MYOCLONIC EPILEPSIES OF ADOLESCENCE AND ADULTHOOD

Familial Juvenile Myoclonic Epilepsy

Genetics of JME:: Faulty Components and Faulty Wiring?

Autosomal Dominant Juvenile Myoclonic Epilepsy and GABRA1

CLCN2 and Idiopathic Generalized Epilepsy

Autosomal Dominant Cortical Myoclonus and Epilepsy (ADCME) With Linkage to Chromosome 2p11.1-Q12.2

Familial Adult-Onset Myoclonic Epilepsy (FAME)

Treatment of Myoclonic Epilepsies in Infancy and Early Childhood

TREATMENT OF MYOCLONIC EPILEPSIES

Ketogenic Diet in Patients with Dravet Syndrome and Myoclonic Epilepsies in Infancy and Early Childhood

Treatment of Myoclonic Epilepsies of Childhood, Adolescence, and Adulthood