Benign Childhood Focal Seizures And Related Epileptic Syndromes
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The Epilepsies by Chrysostomos P. Panayiotopoulos Pdf
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 by Chrysostomos P. Panayiotopoulos Pdf
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.
Author : C. P. Panayiotopoulos Publisher : Springer Science & Business Media Page : 627 pages File Size : 53,9 Mb Release : 2010-05-10 Category : Medical ISBN : 9781846286445
A Clinical Guide to Epileptic Syndromes and their Treatment by C. P. Panayiotopoulos Pdf
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.
Benign Childhood Focal Seizures and Related Epileptic Syndromes by C. P. Panayiotopoulos Pdf
Benign Childhood Focal Seizures and Related Epileptic Syndromes provides a concise, authoritative guide to all aspects of diagnosis, treatment and management of the three identifiable electroclinical syndromes: rolandic epilepsy, Panayiotopoulos syndrome and the idiopathic childhood occipital epilepsy of Gastaut. These have a high prevalence, probably affecting 22% of children with non-febrile seizures and constitute a significant part of the everyday practice of paediatricians, neurologists and electroencephalographers. This pocket-sized reference work will be a valuable resource for all those involved in the care of children with epileptic seizures.
Epilepsy is among the most common scourges afflicting the health of humankind and perhaps the most terrifying. In one form or another, it is suffered by one in everyone hundred people on earth, with a disproportionate prevalence at the early and late extremes of life. There is nothing sacred or sanctifying about it in spite of Hippoc rates' terming epilepsy "The Sacred Disease" in a famous treatise. There is nothing ennobling about it despite its occasional designa tion as a "noble disorder" by virtue of i ts having affected the likes of Alexander of Macedon, Julius Caesar and other persons of royal lineage. From time to time, epilepsy is hailed as a condition which is artistically inspirational; Fyodor Dostoyevsky's dependence on his own personal experience with complex partial epilepsy as a source of imagery in the transfiguration scenes of The Brothers Karamazov and as a source of experience in The Idiot is often cited in this respect. In fact, for all its victims in human history, epilepsy has been a sad burden which has disrupted and shortened life, causing suffering and castigation for the duration of their terrestrial journey.
Panayiotopoulos Syndrome by Chrysostomos P. Panayiotopoulos,Colin D. Ferrie Pdf
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.
Epileptic Syndromes in Infancy, Childhood and Adolescence - 5th edition by Bureau Michelle,Genton Pierre,Dravet Charlotte Pdf
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.
Case Studies in Epilepsy by Hermann Stefan,Elinor Ben-Menachem,Patrick Chauvel,Renzo Guerrini Pdf
This selection of epilepsy case studies will inform and challenge clinicians at all stages in their careers. Including both common and uncommon cases, Case Studies in Epilepsy reinforces the diagnostic skills and treatment decision-making processes necessary to treat epilepsy and other seizures confidently in pediatric and adult patients.
Atlas of Epilepsies by S.R. Benbadis,R.G. Beran,A.T. Berg,J. Engel, Jr.,A.S. Galanopoulou,P.W. Kaplan,M. Koutroumanidis,S.L. Moshe,D.R. Nordli, Jr.,J.M. Serratosa,S.M. Sisodiya,W.O. Tatum,T. Valeta,A. Wilner Pdf
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.
Magnetic Resonance in Epilepsy by Ruben Kuzniecky,Graeme D. Jackson Pdf
Remarkable advances in imaging have increased the importance of MRI for diagnostic, treatment and management of epilepsy. Neuroimaging of patients with epilepsy no longer simply deals with the technology and interpretation of images but also with issues of brain metabolism, energetics, cognition and brain dysfunction. The first edition of Magnetic Resonance in Epilepsy came into clinical practice in 1995 with a revolutionary idea; that is, MR is as important as EEG in the clinical management of patients with epilepsy. The second edition of Magnetic Resonance in Epilepsy, the only comprehensive text in the field of epilepsy neuroimaging, reviews fundamental concepts and new advances in MR technology, computerized analysis, MR spectroscopy, DWI and other neuroimaging techniques such as PET, SPECT and MEG application to the study of patients with epileptic disorders. *Provides a crucial update of recent advances in imaging techniques*Timely publication as subject of neuroimaging is a very "hot" area in both clinical epilepsy and basic neuroscience research*Editors are well-respected in this field
James W. Wheless,Dave F. Clarke,Amy L. McGregor,Philip L. Pearl,Yu-Tze Ng
Author : James W. Wheless,Dave F. Clarke,Amy L. McGregor,Philip L. Pearl,Yu-Tze Ng Publisher : John Wiley & Sons Page : 362 pages File Size : 42,9 Mb Release : 2012-10-22 Category : Medical ISBN : 9781118388518
Epilepsy in Children and Adolescents by James W. Wheless,Dave F. Clarke,Amy L. McGregor,Philip L. Pearl,Yu-Tze Ng Pdf
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.
The book chapters cover different aspects of epilepsy genetics, starting with the "classical" concept of epilepsies as ion channel disorders. The second part of the book gives credit to the fact that by now non-ion channel genes are recognized as equally important causes of epilepsy. The concluding chapters are designed to offer the reader insight into current methods in epilepsy research. Each chapter is self-contained and deals with a selected topic of interest. Authors are the leading experts in the field of epilepsy research Book covers the most important aspects of epilepsy Interesting for both scientists and clinicians
Pediatric Neurology Part I by Federico Vigevano,Nicola Specchio,Natalio Fejerman Pdf
In this chapter we include a series of epilepsies with onset in pediatric age characterized by focal seizures, idiopathic etiology, normal psychomotor development, and a benign course related to the spontaneous remission of seizures without sequelae. These entities are age-dependent and seizures tend to disappear spontaneously. For these reasons often the drug treatment is not necessary. On the basis of genetic assessment idiopathic focal epilepsies can be divided into two groups: nonautosomal dominant and autosomal dominant. In the group of nonautosomal entities we include benign epilepsy with centro-temporal spikes, Panayiotopoulos syndrome, idiopathic childhood occipital epilepsy described by Gastaut, and benign idiopathic midline spikes epilepsy. Seizures are rare, sometimes prolonged, as autonomic status in Panayiotopoulos syndrome. A common feature is the presence of peculiar EEG interictal paroxysmal abnormalities. In the group with an autosomal dominant mode of inheritance we include benign familial infantile seizures and benign familial neonatal–infantile seizures. These entities are characterized by partial seizures in cluster, self-limited in a brief period during the first months of life. There are no typical interictal EEG abnormalities. In some families a mutation in SCN2A, the gene coding for the 2α subunit of the voltage-gated sodium channel, has been described.