The most important advance in recent epileptology is the recognition of epileptic syndromes and diseases, most of which are well defined and easy to diagnose. The benign childhood partial seizures syndromes exemplify the importance of a precise diagnosis and classification of epilepsies. They are common, and have an excellent prognosis which is better than that of febrile convulsions. Paediatricians and clinical neurophysiologists are now familiar with the Rolandic seizures but are not yet accustomed to diagnosing other benign childhood partial seizures and in particular benign childhood occipital seizures which are often confused with cerebral insults or migraine. The aim of this reference book is to describe the clinical and EEG manifestations of benign childhood partial seizures with particular emphasis on the occipital seizures which are often more characteristic, easier to diagnose and, in some cases, more benign than Rolandic seizures.

Book and DVD. The fourth edition of Epileptic syndromes in Infancy, Childhood and Adolescence is based on the syndromic approach to epilepsy that is the trademark of the Marseille School of European epileptology, including new perspectives. The accompanying DVD includes video sequences of the various syndromes.

Affecting 4 percent of children and 1-2 percent of the general population, epilepsy is one of the most common neurological disorders. The 1st edition of this guide proved to be the only one of its kind, covering many important aspects of diagnosis and treatment. Due to the continued advances being made in the subject, and building on the sell-out success of the 1st edition this thorough revision reflects the latest report of the ILAE classification core group and the significant progress made in the diagnosis, classification and treatment of the epilepsies.

Serving as a reference on the epilepsies, this fourth edition provides an overview of seizure disorders and contemporary treatment options. It brings together the vital work in the neurosciences, genetics, electroencephalography, pediatric and adult neurology, neuropharmacology, neurosurgery, and psychiatry. It also talks about epilepsy surgery.

The extensively updated third edition of Pediatric Epilepsy: Diagnosis and Therapy continues to be the definitive volume on the diagnosis, treatment, classification, and management of the childhood epilepsies. Written by nearly 100 international leaders in the field, this new edition progresses logically with major sections on the basic mechanisms of the disease, classification, epidemiology, etiology, diagnosis, and age-related syndromes of epilepsy. The core of the new third edition is its completely updated section on antiepileptic drugs, including an in-depth discussion of dosage considerations, drug toxicity, teratogenicity, and drug interactions, with recommendations for optimal combinations when multiple drug therapy is required. Features unique to the third edition include: Expanded section on the basic science and mechanism of epilepsy Completely updated drug chapters, including newly released drugs and those in development Expanded chapters on vagus nerve stimulation and surgical treatment Expanded section on co-morbidities The third edition includes 21 new chapters, including discussions of: epileptic channelopathies; epileptogenic cerebral cortical malformation; epilepsy genes; etiologies and workup; evidence-based medicine issues related to drug selection; Levetiracetam; Sulthiame; Pregabalin; herbal medications; basic and advanced imaging; immunotherapy issues; vagus nerve stimulation therapy; cognitive and psychiatric co-morbidities and educational placement; and psychosocial aspects of epilepsy.

The aim of the colloquium from which this multi-author book derives, was to outline the specific expression of epilepsies involving the limbic structures in children and to establish a consensus on the evidence relevant to the clinical management of these epilepsies. The book addresses basic questions such as age-related aetiologic, pathogenetic and prognostic factors relevant to the course of infantile epilepsies with limbic seizures, and enlightens the criteria for their clinical and laboratory assessment. The interaction between basic scientists, neuropaediatricians and neurosurgeons contributes to define suitable strategies aimed at preventing the unfavourable course of these often severe infantile epilepsies and their optimal timing.

In one convenient source, this book provides a broad, detailed, and cohesive overview of seizure disorders and contemporary treatment options. For this Fifth Edition, the editors have replaced or significantly revised approximately 30 to 50 percent of the chapters, and have updated all of them. Dr. Wyllie has invited three new editors: Gregory Cascino, MD, FAAN, at Mayo Clinic, adult epileptologist with special expertise in neuroimaging; Barry Gidal, PharmD, at University of Wisconsin, a pharmacologist with phenomenal expertise in antiepileptic medications; and Howard Goodkin, MD, PhD, a pediatric neurologist at the University of Virginia. A fully searchable companion website will include the full text online and supplementary material such as seizure videos, additional EEG tracings, and more color illustrations.

Epilepsy seems to represent one of the most frequent neurological diseases and occurs in about 1% of the general population. Although epilepsy is known since antiquity, the precise data on its pathogenesis and effective treatment are still collected and nowadays represents an interest for neurologists and psychiatrists. Being a neurological disease, epilepsy is characterized by a broad palette of comorbid psychiatric disorders (affective and anxiety disorders, psychoses) that reduce the quality of life. Moreover, the risk of suicidal attempts in persons with epilepsy is much higher than in general population that once again increases the actuality of epilepsy research in many aspects. The book contains 13 chapters written by different authors from all over the world on different topics, including phenomenology, pathogenesis, and treatment in epilepsy. The modern data on these topics may be helpful for many specialists in the domain of epileptology.

Accurate diagnosis of neurological disorders can often be difficult due to the complex nature of the nervous system. Whilst technological advances have greatly improved diagnostic and interpretation techniques, errors can still occur, which consequently result in mistakes in therapeutic care. This book is a guide to diagnostic strategies for a multitude of common and less common neurological disorders. Scenarios are set in both a clinical and an intensive care setting. Divided into 13 sections, the text begins with an overview of general neurology. Each of the following sections examines disorders in a different part of the nervous system. Diagnostic processes are evaluated and potential areas where a clinician may make a mistake, are examined and explained in depth. The final section presents 15 authentic cases covering diagnostic challenges in critical care units, all provided by leading experts from the University of Texas Southwestern Medical Centre, USA. With contributions from internationally recognised neurologists, this comprehensive text is highly illustrated with neurological images, and many chapters feature additional editorial notes and appendices. Access to a selection of clinical videos via a QR code is also provided with this book.