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.

This second edition of 'Seizures and Epilepsy' is completely revised, due to tremendous advances in the understanding of the fundamental neuronal mechanisms underlying epileptic phenomena, as well as current diagnosis and treatment, which have been heavily influenced over the past several decades by seminal neuroscientific developments, particularly the introduction of molecular neurobiology, genetics, and modern neuroimaging. This resource covers a broad range of both basic and clinical epileptology.

Epilepsy in childhood presents a profound challenge Epilepsy is an unsettling, complex condition. There is no ‘one size fits all’ option. For effective treatment a full understanding of each patient’s situation and clinical history is needed. Recent remarkable improvements in our ability to image brain structures, to define physiological patterns and in treatment options has made the task of care of the child with epilepsy potentially more effective. Epilepsy in Children and Adolescents provides the contemporary, caring guidance you need to diagnose and manage seizures in a young patient. Beginning with an overview of the classification of epilepsy syndromes, the experienced authors cover: Diagnostic evaluation of childhood epilepsies Principles of treatment Generalized seizures and generalized epilepsy syndromes Partial onset seizures and localization-related epilepsy syndromes Epilepsies relative to age, etiology or duration The full range of treatment options: medical, dietary, surgical Epilepsy in Children and Adolescents takes a practical approach to a common but complex clinical challenge.

Easy to read and richly illustrated, Atlas of Clinical Sleep Medicine, 3rd Edition, provides the tools you need to accurately diagnose and treat the full range of adult and pediatric sleep disorders. Dr. Meir H. Kryger and a team of expert contributing authors detail the physiologic, clinical, morphologic, and investigational aspects of the sleep disorders you encounter in everyday practice—enhanced by high-quality images throughout. This highly regarded, award-winning atlas is an ideal resource for sleep practitioners and technicians in the lab, as well as an effective review for certification and recertification. - Features a thoroughly illustrated, reader-friendly format that highlights key details, helping you interpret the visual manifestations of your patients' sleep disorders so you can manage them most effectively. - Contains the most up-to-date drug therapy with information about the latest drugs available as well as those in clinical trials. - Provides greater coverage of pediatric and adolescent disorders, including behavioral insomnia, new medication options, and multiple sleep latency testing (MSLT) specific to children. - Includes current AASM scoring guidelines and diagnostic criteria. - Presents correlations between normal and abnormal sleep relative to other health issues such as stroke and heart failure. - Illustrates the physiology of sleep with full-color images (many are new!) and correlates the physiology with the relevant findings. - Provides numerous resources online, including more than 80 patient interview and sleep lab videos and 200+ polysomnogram fragments.

'---~~~~-~~---------------. . . . . . . . . -. . . . . . . . . . . . . . . . . . . -. . . . . . . . . . . . . . . . . . . . . . . . . 41 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ••••••• he year 2001 marks the beginning of a new millenium, and (chromosome 1) result in dominantly inherited AD. A major risk T the second edition of the Atlas of Clinical Neurology high factor for AD is the presence of the E4 allele of apolipoprotein E lights and underscores the enormous strides being made in (chromosome 19). Additional detailed images related to the the biologic understanding of neurologic disease. Neurology is a dementias are included in the second edition of the Atlas. These highly visual specialty. The neurologic examination, magnetic reso clinical-molecular correlations are all very recent and attest to the nance imaging, electroencephalography, positron-emission tomo scientific vigor of current neuroscientific research. It is my view that graphic (PET) and functional magnetic resonance (fMRI) scan these new data will lead in the near future to effective new therapy ning, and light- and electron-microscopy are examples of visual for AD that will slow its rate of progress and reduce significantly images that define neurologic disease and normal brain functions. the incidence of this major, debilitating disease. Positron-emission This Atlas of Clinical Neurology has been designed to provide a pic tomographic and fMRI brain scanning have effectively defined torial comprehensive visual exposition and integration of all aspects regional brain areas for behaviors.

Providing a pictorial representation of this common and chronic disorder of the nervous system, this revision of the best-selling Atlas of Epilepsy complements existing textbooks. Covering diagnosis by EEG, pathology and neuroimaging, plus valuable material on prognosis and management, the second edition of this highly acclaimed title builds on the success of its predecessor to include: many new images radically improved and updated neuroradiology scans a complete update of the section on therapy images that are fully integrated with the text, thus improving the work’s the visual and didactic impact. Useful as a source of illustrations for neurologists, this is also an excellent introduction to epilepsy for trainees, primary care practitioners and family medicine practitioners.

"Electroencephalography (EEG) is an invaluable tool for evaluating patients with suspected seizures or encephalopathy, yet EEG is only one source of data, so information from this technology must be integrated with knowledge of basic science and clinical neurology. This work has a principal focus on EEG, but interleaves that discussion with information on seizures, epilepsy, encephalopathy, and other neurologic conditions for which EEG can be a useful diagnostic tool"--

Epilepsy is one of the most common serious disorders of the brain, affecting about 50 million people worldwide. Epilepsy accounts for 1 per cent of the global burden of disease; 80 per cent of the burden of epilepsy is in the developing world, where in some areas 80-90 per cent of people with epilepsy receive no treatment at all. The Epilepsy Atlas provides an illustrative presentation of data and information on the current status of epilepsy services and care available from 160 countries, areas or territories covering 97.5 per cent of the world population. The information is primarily gathered from key persons in the area of epilepsy care in each country identified by International Bureau for Epilepsy and the International League against Epilepsy, and, in some cases, by WHO regional offices.

The need for neuropathology reviews in epilepsy surgery tissues steadily increases. However, textbooks and case presentations highlighting and focusing on this specific topic are rare. The authors of this book reviewed their professional experience in surgical and post-mortem neuropathology studies to compile a coherent summary of: clinico-pathological findings, current classification schemes, useful protocols research data for major histopathological entities of brain lesions encountered in modern epilepsy surgery programs, which is hippocampal sclerosis, brain tumours associated with early epilepsy onset, malformations of cortical development, brain inflammation and malformative vascular lesions. They did not intend to be exhaustive but rather representative of the main lesions and pathologies encountered. Thirty-two illustrated cases constitute the core of this book and will be very helpful in current practice.

Interdisciplinary co-operation between epileptologists, neuroradiologists, psychologists and neurosurgeons is the most fundamental prerequisite for localising and performing targeted resections of epileptogenic foci from patients with focal therapy resistant epilepsy. Worldwide there has been a steady increase in the number of epilepsy surgery centres, and in the number of operations performed on children and babies. A systematic neuropathological description is presented here involving macroscopic and histological findings. In this book, a systematic documentation of characteristic as well as rarer alterations is presented involving 444 patients who had been operated on in Germany between 1990 and 1997 at the Bethel Epilepsy Centre in Bielefeld. It includes 257 patients with temporal lobes (TLE) and 187 patients with extratemporal epilepsy (ETE).