Idiopathic generalised epilepsies

Häftad, Engelska, 2012

479 kr

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Beskrivning

Idiopathic generalised epilepsies provides a concise, authoritative guide to this category of epilepsies. Each syndrome of idiopathic generalised epilepsy is detailed in regard to demographic data, clinical manifestations, aetiology, diagnosis, prognosis and management.

Produktinformation

Utgivningsdatum:2012-06-22
Mått:155 x 235 x 8 mm
Vikt:188 g
Format:Häftad
Språk:Engelska
Antal sidor:83
Förlag:Springer London Ltd
ISBN:9781447140382
Originaltitel:A Clinical Guide to Epileptic Syndromes and their Treatment, Revised Second Edition

Utforska kategorier

Neurologi och klinisk neurofysiologi inom Medicin

Mer om författaren

C. P. Panayiotopoulos is an internationally renowned leader and expert in the diagnosis, treatment and management of epilepsy. C. P. Panayiotopoulos is currently practising as Locum Consultant Neurologist on epilepsies at John Radcliffe Hospital, Oxford and remains Consultant emeritus at St. Thomas' Hospital, London where he has served over the last 20 years as a Consultant in Clinical Neurophysiology and Epilepsies.

Recensioner i media

From the reviews: "This monograph covers the main clinical, diagnostic, therapeutic, and prognostic features of the genetic generalized epilepsy (GGE) syndromes in early childhood through adulthood. ... this book perfect for busy residents, pediatricians, neurologists, neurosurgeons, and allied healthcare professionals interested in GGE. ... it is recommended to physicians in training and busy clinicians who are interested in learning the intricacies of common syndromes to avoid the pitfalls of 'lumping' patients with generalized seizures under the rubric of idiopathic generalized epilepsy." (William Tatum, Doody's Book Reviews, February, 2013)

Innehållsförteckning

Introduction.- Syndromes of IGE recognised by the ILAE.- Epilepsy with myoclonic–astatic seizures.- Childhood absence epilepsy.- Epilepsy with myoclonic absences.- Juvenile absence epilepsy.- Juvenile myoclonic epilepsy.- Epilepsy with GTCSs only.- Other probable syndromes of IGE to consider.- IGE with absences of early childhood.- Perioral myoclonia with absences.- IGE with phantom absences.- Autosomal dominant cortical tremor, myoclonus and epilepsy.- AED treatment of IGEs.