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Author: Bettina Schmitz Publisher: Routledge ISBN: Category : Medical Languages : en Pages : 232
Book Description
This is the first book to deal comprehensively with this fascinating idiopathic epileptic syndrome. Juvenile myoclonic epilepsy, thought to account for up to 11% of all epilepsies, is characterized by bilateral myoclonic jerks of the limbs, usually without loss of consciousness, which occur in otherwise healthy individuals, generally shortly after awakening. JME displays a clear genetic basis and episodes can be precipitated by lack of sleep, irregular lifestyle or by certain manual activities.The book is divided into three sections. The first and largest section addresses clinical aspects of JME including epidemiology, definitions, and diagnosis, electrophysiology, imaging and radiology, psychological and psychiatric aspects, and treatment. Section 2 examines clinical genetics and teratology, and Section 3 looks in detail at the molecular genetics of JME, the area in which research is most active.This volume brings together the leading international names in a particularly intriguing area of epilepsy,research. The contributors include famous authors from UK, USA, Japan, Germany, Italy and France. The concluding chapter is by Dieter Janz who was the first author to describe JME in 1957.
Author: Bettina Schmitz Publisher: Routledge ISBN: Category : Medical Languages : en Pages : 232
Book Description
This is the first book to deal comprehensively with this fascinating idiopathic epileptic syndrome. Juvenile myoclonic epilepsy, thought to account for up to 11% of all epilepsies, is characterized by bilateral myoclonic jerks of the limbs, usually without loss of consciousness, which occur in otherwise healthy individuals, generally shortly after awakening. JME displays a clear genetic basis and episodes can be precipitated by lack of sleep, irregular lifestyle or by certain manual activities.The book is divided into three sections. The first and largest section addresses clinical aspects of JME including epidemiology, definitions, and diagnosis, electrophysiology, imaging and radiology, psychological and psychiatric aspects, and treatment. Section 2 examines clinical genetics and teratology, and Section 3 looks in detail at the molecular genetics of JME, the area in which research is most active.This volume brings together the leading international names in a particularly intriguing area of epilepsy,research. The contributors include famous authors from UK, USA, Japan, Germany, Italy and France. The concluding chapter is by Dieter Janz who was the first author to describe JME in 1957.
Author: John S. Duncan Publisher: John Libbey Eurotext ISBN: 9780861965502 Category : Medical Languages : en Pages : 146
Book Description
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.
Author: Antonio V. Delgado-Escueta Publisher: Lippincott Williams & Wilkins ISBN: 9780781752480 Category : Medical Languages : en Pages : 368
Book Description
This 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.
Author: C. P. Panayiotopoulos Publisher: Springer Science & Business Media ISBN: 1846286441 Category : Medical Languages : en Pages : 627
Book Description
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.
Author: Michalis Koutroumanidis Publisher: John Libbey Eurotext ISBN: 2742015744 Category : Medical Languages : en Pages : 271
Book Description
This book, written by international experts in clinical epileptology and EEG, comprehensively covers the clinical and EEG features of all paediatric and adult epilepsy syndromes, as recognized by the ILAE. Each syndrome-chapter provides detailed description of the associated seizure types and the characteristic interictal findings in wakefulness and sleep, illustrated by a plethora of EEG plates. It also includes recording protocols that, adapted to available resources and complete with practical information to improve recording strategies, are designed to maximize diagnostic yield. Finally, the diagnostic confidence of the EEG report is rated according to the findings in hand and the available clinical information. A fully informative, but concise and easy-to-use, companion in the daily clinical practice for electroencephalographers and EEG technologists, but also a reference guide for epileptologists and general neurologists who care for children and adults with epilepsy.
Author: Bureau Michelle Publisher: John Libbey Eurotext ISBN: 2742008292 Category : Medical Languages : en Pages : 682
Book Description
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.
Author: S.R. Benbadis Publisher: Springer Science & Business Media ISBN: 1848821271 Category : Medical Languages : en Pages : 1966
Book Description
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 internationally-renowned experts, and is liberally interspersed with clinical insights and personal vignettes that offer helpful tips, technical advice and critical knowledge to the clinician and scholar. The thorough and complete table of contents includes dedicated sections or chapters on important topics such as neonatal and pediatric seizures; imitators of epilepsy; EEG and neuroimaging; psychiatric and quality of life aspects of epilepsy; and a complete guide to treatment options including current and up-to-date chapters on pharmaceuticals, surgical procedures, and additional and alternative treatments. No other publication addresses epilepsies as thoroughly and completely as the Atlas of Epilepsies. Exhaustive and illustrative, convenient and current, this reference is sure to be the premier text on epilepsy for many years to come.
Author: Ivan Donaldson Publisher: Oxford University Press ISBN: 0191502243 Category : Medical Languages : en Pages : 1512
Book Description
This book represents the final work of the late Professor C. David Marsden, who was the most influential figure in the field of movement disorders, in terms of his contributions to both research and clinical practice, in the modern era. It was conceived and written by David Marsden and his colleague at the Institute of Neurology, Prof. Ivan Donaldson. It was their intention that this would be the most comprehensive book on movement disorders and also that it would serve as the 'clinical Bible' for the management of these conditions. It provides a masterly survey of the entire topic, which has been made possible only by vast laboratory and bedside experience. Marsden's Book of Movement Disorders covers the full breadth of movement disorders, from the underlying anatomy and understanding of basal ganglia function to the diagnosis and management of specific movement disorders, including the more common conditions such as Parkinson's Disease through to rare, and very rare conditions such as Niemann-Pick disease. Chapters follow a structured format with historical overviews, definitions, clinical features, differential diagnosis, investigations and treatment covered in a structured way. It is extensively illustrated with many original photographs and diagrams of historical significance. Among these illustrations are still images of some original film clips of some of Dr. Marsden's patients published here for the first time. Comprehensively referenced and updated by experts from the Institute of Neurology at Queen Square, this book is a valuable reference for, not just movement disorder specialists and researchers, but also for clinicians who care for patients with movement disorders.
Author: Bettina Schmitz
Author: Bettina Schmitz
Author: John S. Duncan
Author: Antonio V. Delgado-Escueta
Author: C. P. Panayiotopoulos
Author: Michalis Koutroumanidis
Author: Gonzalo Alarcón
Author: Simon Shorvon
Author: Bureau Michelle
Author: S.R. Benbadis
Author: Ivan Donaldson