The current concept of dystonic movement connects the abnormal function of somatosensory pathways and somatosensory analyzers with the dystonic performance of motor action, which is based on the abnormality of sensorimotor integration. This concept is reflected not only in idiopathic dystonia, but also in secondary and symptomatic dystonias. This bookwill give a comprehensive account ofthe history of the terms dystonia and dystonic, the physiology of dystonic movement, and the genetics and clinical appearance of primary and secondary dystonias. Taking into considerationlatest research findings, Dystonia and Dystonic Syndromes offers an in-depth discussion of current treatment options available for dystonia, including pharmacotherapy, surgery, and neurorehabilitation. Therefore, it serves as a valuable reference for practitioners in the fields of neurology, neurosurgery, psychiatry, and neuroradiology as well as for neuroscientists.

The neurologic subspecialty of Movement Disorders is complicated with many different entities, making the differential diagnosis difficult. One of the most important aspects of these different entities is their visual appearance. Still photographs do not give sufficient information, but videos like the ones included in this volume can provide dimension, context, and critical information. The variety of visual appearances is wide and seeing many videos is necessary to develop skill in making a diagnosis. Involuntary movements are even more complicated and the adage "seeing is believing" has never been more true. Despite this, few books include videos portraying involuntary movements. Involuntary Movements: Classification and Video Atlas pairs descriptions of the clinical features of various involuntary movements with video depictions of the involuntary movements in action. In a unique approach, this book considers two aspects of the diagnosis of involuntary movements: the phenomenology - as depicted in approximately 200 video supplements - and the etiology. The book also discusses the current consensus on the classification, pathophysiology, and treatment of each involuntary movement.

This issue reviews the role of metals in neurodegenerative diseases; including Parkinson s and Huntington s disease; restless leg syndrome and NBIA disorders; and Wilson s disease and manganese and calcium accumulation disorders. An update on advances in neuroimaging and pathology of metal related diseaseis also presented.

This volume of "International Review of Neurobiology" brings together cutting-edge research on metal related neurodegenerative disease. It reviews the role of metals in neurodegenerative diseases, including Parkinson s and Huntington s disease; restless leg syndrome and NBIA disorders; and Wilson s disease and manganese and calcium accumulation disorders. An update on advances in neuroimaging and pathology of metal related diseaseis also presented. "

This is the second edition of the Oxford Specialist Handbook in Parkinson's Disease and Other Movement Disorders aiming to provide its readership with the latest developments and innovation across the discipline. Alongside this update in content, the addition of new, insightful sections suggested by readers and other experts in the field, will allow the handbook to further develop as the premier quick reference guide for movement disorders. The varied and detailed composition of the handbook's chapters is extremely useful for the various readership of this title. The new edition advances the the knowledge and depth of the previous edition with the addition of a number of new sections. This new and improved edition will be a welcome and extremely useful addition to the neurological world.

Drawing on the expertise of an international team of authors, Case Studies in Movement Disorders is a compilation of illustrative cases, demonstrating a step-by-step approach to diagnosing and managing these complex conditions. An extensive collection of over sixty videos shows both common and uncommon presentations of a wide range of movement disorders, and the accompanying text guides readers systematically through the clinical history, examination and investigation findings, and diagnosis, and finally discusses the clinical issues raised. Both surgical and pharmacological management options are presented, helping readers understand some of the controversies involved in treatment. The cases are drawn from all of the major groups of movement disorders: ataxia, chorea, dystonia, myoclonus, parkinsonism, tics, and tremor. This will be invaluable for both neurologists in training and more experienced professionals seeking to develop their diagnostic skills, especially when faced with uncommon conditions or uncommon manifestations of common disorders.