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020 _z9780781752480
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050 4 _aRC372 -- .M963 2005eb
082 0 _a616.853
100 1 _aDelgado-Escueta, Antonio V.
245 1 0 _aMyoclonic Epilepsies :
_bUnderstanding Its Nature, Diagnosis and Treatment.
250 _a1st ed.
264 1 _aPhiladelphia :
_bWolters Kluwer Health,
_c2004.
264 4 _c©2004.
300 _a1 online resource (304 pages)
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
490 1 _aAdvances in Neurology ;
_vv.95
505 0 _aCover -- Copyright -- Editeds -- Editors -- Advances in Neurology Series -- Charlotte Dravet -- Preface -- Foreword -- Acknowledgments -- Contents -- Section 1 Introduction to Concepts and Classifications -- 1 History and Classification of "Myoclonic" Epilepsies: From Seizures to Syndromes to Diseases -- 2 Ontogeny of the Reticular Formation: Its Possible Relation to the Myoclonic Epilepsies -- 3 Pathophysiology of Myoclonic Epilepsies -- 4 Progressive Myoclonus Epilepsies: EPM1, EPM2A, EPM2B -- 5 Myoclonic Status in Nonprogressive Encephalopathies -- Section 2 Myoclonic Epilepsies of Infancy and Childhood -- 6 Severe Myoclonic Epilepsy in Infancy: Dravet Syndrome -- 7 Severe Myoclonic Epilepsy in Infancy: Clinical Analysis and Relation to SCN1A Mutations in a Japanese Cohort -- 8 Myoclonic Seizures in the Context of Generalized Epilepsy with Febrile Seizures Plus (GEFS+) -- 9 Benign Myoclonic Epilepsy in Infancy -- 10 Autosomal Recessive Benign Myoclonic Epilepsy of Infancy -- 11 Myoclonic-Astatic Epilepsy of Early Childhood - Definition, Course, Nosography, and Genetics -- 12 Idiopathic Myoclonic-Astatic Epilepsy of Early Childhood-Nosology Based on Electrophysiologic and Long-Term Follow-Up Study of Patients -- 13 Myoclonic Absences: The Seizure and The Syndrome -- 14 Eyelid Myoclonia and Absence -- 15 Childhood Absence Epilepsy Evolving to Juvenile Myoclonic Epilepsy: Electroclinical and Genetic Features -- 16 Photosensitivity: Genetics and Clinical Significance -- Section 3 Myoclonic Epilepsies of Adolescence and Adulthood -- 17 Familial Juvenile Myoclonic Epilepsy -- 18 Genetics of Juvenile Myoclonic Epilepsy: Faulty Components and Faulty Wiring? -- 19 Autosomal Dominant Juvenile Myoclonic Epilepsy and GABRA1 -- 20 CLCN2 and Idiopathic Generalized Epilepsy.
505 8 _a21 Autosomal Dominant Cortical Myoclonus and Epilepsy (ADCME) with Linkage to Chromosome 2p11.1-q12.2 -- 22 Familial Adult Myoclonic Epilepsy (FAME) -- Section 4 Treatment of Myoclonic Epilepsies -- 23 Treatment of Myoclonic Epilepsies in Infancy and Early Childhood -- 24 Ketogenic Diet in Patients with Dravet Syndrome and Myoclonic Epilepsies in Infancy and Early Childhood -- 25 Treatment of Myoclonic Epilepsies of Childhood, Adolescence, and Adulthood.
520 _aThis 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.
588 _aDescription based on publisher supplied metadata and other sources.
590 _aElectronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2024. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.
650 0 _aEpilepsy.
655 4 _aElectronic books.
700 1 _aGuerrini, Renzo.
700 1 _aMedina, Marco T.
700 1 _aGenton, Pierre.
700 1 _aBureau, Michelle.
700 1 _aDravet, Charlotte.
776 0 8 _iPrint version:
_aDelgado-Escueta, Antonio V.
_tMyoclonic Epilepsies
_dPhiladelphia : Wolters Kluwer Health,c2004
_z9780781752480
797 2 _aProQuest (Firm)
830 0 _aAdvances in Neurology
856 4 0 _uhttps://ebookcentral.proquest.com/lib/orpp/detail.action?docID=2032532
_zClick to View
999 _c49989
_d49989