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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.
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.
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.
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