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Myoclonic Epilepsies
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This volume is the first comprehensive text and clinical reference on idiopathic myoclonic epilepsies of infancy, childhood, adolescence, and adulthood. The world’s foremost experts describe the phenotypes and subtypes of myoclonic epilepsies and the underlying molecular defects and summarize cutting-edge advances in molecular genetics that shed new light on the etiologies of these syndromes.
The book offers clinicians much-needed assistance in recognizing and diagnosing idiopathic myoclonic epilepsies and selecting appropriate treatment. Each chapter includes diagnostic and treatment algorithms to guide practitioners in clinical decision making.
Data sheet
- Publication date
- 2004
- Issue number
- 1
- Cover
- hard cover
- Pages count
- 347
- Dimensions (mm)
- 178 x 254
- Weight (g)
- 794
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
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