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Epileptic Syndromes in Infancy, Childhood and Adolescence
This text examines epileptic syndromes in infancy, childhood and adolescence.
Falls in Epileptic and Non Epileptic Seizures During Childhood
At the Mariani Foundation meeting held in Milan, October 1995, highly qualified specialists were invited to assist in understanding of the basic principles of cerebral development and brain function, with specific attention to those structures and mechanisms involved in the phenomenon of falls. Epiliptologists illustrate the different semiologic modalities and clinical conditions in which the fall is an essential symptom. A main part of the book is dedicated to the medical and surgical treatment of syndromes where falls appear in the foreground. This volume has the mission of improving life conditions of children who suffer from drop seizures, by limiting the risks to which they are subjected, and to try and compensate for the psychological and social limitations affecting them.
Prognosis of Epilepsies
The last book on the prognosis of epilepsies was written by Rodin in 1968. For the next 35 years, many original papers or chapters in textbooks were published on this complex topic. Most of these endeavours, reflecting the clinician's highly detailed point of view were based on selected cases with little concern for the epidemiological context or upon the epidemiologist's population-based approach which tends to ignore important clinical details. Until quite recently, fundamental epidemiological aspects of epilepsy, as it is understood by clinicians, have not been explored, and clinicians viewed populationbased epidemiology as relatively irrelevant to their daily practice. This book is divided into two majors parts. Presentations in the first part address methodological issues regarding prognostic studies (including remission and mortality) as well as results from long-term cohort studies. The second part contains presentations on the clinical aspects and prognosis of several individual epilepsy syndromes as well as presentations about the prognosis of status epilepticus and outcome of frontal and temporal lobe surgery.
Genetics of Focal Epilepsies
This volume contains contributions on genetic aspects of a wide range of focal epilepsies. It is based on an international workshop held in Avignon, France in September 1996. Topics covered include: idiopathic age-related focal epilepsies; idiopathic iocal epilepsies in infancy; autosomal dominant focal epilepsies; molecular biology; animals models; and case reports.
Syndromes épileptiques de l'enfant et de l'adolescent - 5eme edition
Un DVD inclus avec des séquences vidéos inédites pour chaque chapitre ! L’épileptologie change, et les approches syndromiques sont maintenant complétées par une approche étiologique fondée sur les progrès considérables en génétique. Une approche purement « électro-clinique » n’est plus adaptée aujourd’hui dans bien des cas. Cette 5e édition du « Guide bleu » fait le point sur les plus récents progrès. Ainsi, la structure du livre a un peu évolué, laissant plus de place aux approches : - physiologiques - épidémiologiques - génétiques - thérapeutique Néanmoins, la description des syndromes épileptiques reste au cœur de cet ouvrage. La diversité des contributeurs – coordinateurs et auteurs – confère à ce livre des qualités d’objectivité et de sérieux qui en font la réputation depuis maintenant près de 30 ans.
Dictionary of French Family Names in North America
This dictionary contains data not only on the origins of French surnames in Québec and Acadia, a great many of which eventually spread to many parts of North America, but also on those which arrived in the United States directly from various French-speaking European and Caribbean countries. In addition to providing the etymology of the original surnames, it also lists the multifarious variants that have developed over the last four centuries. A unique feature of this work in comparison to other onomastics dictionaries is the inclusion of genealogical information on most of the Francophone migrants to this continent, something which has been rendered possible not only by the excellent record-keeping in French Canada since the very beginnings of the colony, but also through the explosion of such data on the internet in the last couple of decades. In sum, this dictionary serves the dual purpose of providing information on the meanings of French family names on the North American continent, as well as on the migrants who brought them there.
Idiopathic Generalized Epilepsies
Idiopathic generalised epilepsies are characterised by strong genetic factors and multiple clinical phenotypes; animal models of untreated epilepsies are relevant to some of the clinical syndromes found in humans. This volume is the first to confront human clinical, animal (experimental) as well as basic and applied genetic data. Main section headings: Current approaches; Familial neonatal and infantile convulsions; Absence seizures and absence epilepsy; Juvenile myoclonic epilepsy and related syndromes; Photosensitivity; Pathophysiology of convulsive seizures; Fundamental and therapeutic aspects.
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.
