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The Epilepsies
This book gives an exhaustive account of the classification and management of epileptic disorders. It provides clear didactic guidance on the diagnosis and treatment of epileptic syndromes and seizures through thirteen chapters, complemented by a pharmacopoeia and CD ROM of video-EEGs.
Benign Childhood Partial Seizures and Related Epileptic Syndromes
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.
A Clinical Guide to Epileptic Syndromes and their Treatment
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.
Panayiotopoulos Syndrome
Details advanced knowledge on clinical and EEG aspects of Panayiotopoulos syndrome, that affects 6 percent of children with epileptic seizures and it is entirely benign. The spectrum of EEG with occipital and often extra-occipital spikes is richly illustrated as an EEG atlas. Relations with Rolandic, other childhood seizure susceptibility syndromes and Gastaut type idiopathic occipital epilepsy are analytically studied. Panayiotopoulos details the clinical and EEG manifestations, prevalence, pathophysiology and management of 'Panayiotopoulos syndrome' as it emerged from his long-term prospective studies of the author and worldwide documentation through independent studies. He masterly describes the particular type of seizure associated with his syndrome. Panayiotopoulos makes this book a reference for specialists.
Atlas of Epilepsies
Atlas of Epilepsies is a landmark, all-encompassing, illustrated reference work and hands-on guide to the diagnosis, management and treatment of epilepsy in all its forms and across all age groups. The premier text in the field with over one thousand images, the Atlas’s highly illustrative approach tackles the difficult subject of epileptic seizures and epileptic syndromes, accompanied by sequential photographs of each management step. Intraoperative photographs are accompanied by detailed figure legends describing nuances, subtleties, and the thought processes involved in each step, providing a fuller understanding of each procedure. The Atlas draws on the expertise of over 300 internatio...
The Epilepsies
This title will be an exhaustive and thorough text on the range of epileptic conditions, aiming to be the standard reference text on epilepsies for neurologists. It presents established views and recent advances in epileptic seizures and syndromes and their management, and the content is based on the classification, practice parameters and guidelines issued by the International League Against Epilepsy and other recognised medical authorities.
Eyelid Myoclonia with Absences
Eyelid myoclonia with absences is a recently described and under-recognised syndrome of idiopathic generalised epilepsy. The diagnosis may be confused with tics, attempts at self induction, and epilepsy syndromes with a better prognosis such as childhood absence epilepsy. This book summarises current knowledge on the topic; covering the underlying anatomy and physiology of the eyelids, the clinical and electro-encephalographic features and differential diagnosis in children and adults, including a discussion on the issue of self-induction of absences. The current state of knowledge on inheritance and genetics of the condition and treatment strategies are considered. Throughout, recent advances in the field are couched in an historical context, making this book a comprehensive source for all those who need to understand this syndrome whether from a research standpoint or the clinical management of affected children and adults. As such it will be of value to neurologists, epileptologists and those involved in the care and treatment of epileptic patients.
Introduction to Epilepsy
Covers all aspects of epilepsy, from basic mechanisms to diagnosis and management, as well as legal and social considerations.
Antiepileptic Drugs, Pharmacopoeia
Antiepileptic Drugs, Pharmacopoeia provides a concise guide to the properties and clinical applications of all antiepileptic drugs (AED) currently used in the prophylactic treatment of epileptic seizures. The presentation of each AED follows a clinically orientated template. This is in accordance with the FDA Package insert and the EMA Summary of Product Characteristics, supplemented with recent published reports and expert clinical advice. This pocket-sized, user-friendly guide will be a valuable resource for all those involved in the care of patients with epileptic seizures.
Epileptic Syndromes in Infancy, Childhood and Adolescence - 5th edition
The ultimate reference book : the 5th updated edition of the famous “blue guide”. Incluided : A DVD with new sequences completes each chapter! Epileptology changes. The syndromic approach is completed by an etiological approach, based on the major advances in genetics and functional genetics. New entities have found their place, and a purely descriptive, “electroclinical” approach is no longer adapted in many circumstances. The 5th edition of the Blue Guide includes the most recent advances. It was necessary to justify the physiological, epidemiologic, genetic and therapeutic approaches and to consider them in the light of the new classification efforts, which are still in the making. Nevertheless, the description of epileptic syndromes, both classical and recent, remains at the core of this book.
