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Myoclonic Epilepsies

9780781752480
617,40 zł
555,66 zł Zniżka 61,74 zł Brutto
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Opis

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.

Szczegóły produktu
Lippincott Williams & Wilkins
42307
9780781752480
9780781752480

Opis

Rok wydania
2004
Numer wydania
1
Oprawa
twarda
Liczba stron
347
Wymiary (mm)
178 x 254
Waga (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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