Malattie neuromuscolari
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Hyperkinetic Movement Disorders
Differential Diagnosis and Treatment, with Desk Top Edition
Alberto Albanese , Joseph Jankovic
editore: Wiley-Blackwell (an imprint of John Wiley & Sons Ltd)
pagine: 402
Hyperkinetic movement disorders comprise a range of diseases characterized by unwanted and uncontrollable, or poorly controllable, involuntary movements. The phenomenology of these disorders is quite variable encompassing chorea, tremor, dystonia, myoclonus, tics, other dyskinesias, jerks and shakes. Discerning the underlying condition can be very difficult given the range and variability of symptoms. But recognizing the phenomenology and understanding the pathophysiology are essential to ensure appropriate treatment. Hyperkinetic Movement Disorders provides a clinical pathway for effective diagnosis and management of these disorders. The stellar international cast of authors distils the evidence so you can apply it into your practice. The judicious use of • diagnostic criteria • algorithms • rating scales • management guidelines provides a robust framework for clear patient management. Throughout the text, QR codes provide smartphone access to case-study videos of hyperkinetic symptoms. Purchase includes an enhanced Wiley Desktop Edition.
This is an interactive digital version featuring: • all text and images in fully searchable form • integrated videos of presentations - View a sample video: www.wiley.com/go/albanese • highlighting and note taking facilities • book marking • linking to additional references Hyperkinetic Movement Disorders provides you with the essential visual and practical tools you need to effectively diagnose and treat your patients. Full instructions for using QR codes and for downloading your digital Wiley DeskTop Edition are inside the book.
La riabilitazione delle paralisi del VII nervo cranico. Teorie e proposte terapeutiche
Michele Lotter , Antonio Quinci
editore: Piccin-Nuova Libraria
pagine: 284
Tyldesley and Grieve's Muscles, Nerves and Movement in Human Occupation
Barbara Tyldesley
,
Gail Carin-Levy
e altri
editore: Wiley-Blackwell (an imprint of John Wiley & Sons Ltd)
pagine: 376
Now in its fourth edition 'Tyldesley and Grieve's Muscles, Nerves and Movement' has established itself as the leading textbook for the study of movement by occupational therapists. The book provides students with a sound understanding of the way in which bones, joints, muscles and nerves allow the body to perform movement during daily activities. Early chapters provide a foundation for the study of movement, with the complexity of detail increasing as the book progresses. Functional anatomy is related to the movements of daily living and is supported by activities for experiencing and observing the way we perform everyday tasks. Later chapters consider the integration of sensory and motor processes for the planning and execution of movement. This fourth edition has been extensively updated and revised. Highly illustrated and now in full colour throughout the book also includes: • Case histories with self assessment exercises • Summary boxes • Key terms • Practice notepads
Movement Disorders
David G. Standaerdt
,
Jose A. Obeso
e altri
editore: McGraw-Hill Medical
pagine: 1033
A comprehensive clinical reference on managing the entire spectrum of movement disorders NEW DVD with video clips Featuring contributions from more than one hundred of the field's leading experts, this full-color text covers the pathophysiology, diagnosis, and management of all types of movement disorders - from ataxia to Parkinson's Disease. Movement Disorders also examines the neurobehavioral changes and comorbidities that frequently occur and incorporates the latest genetic information and the most current references. Each disease-oriented chapter is organized around sections that include Clinical Presentation and Course, Pathophysiology, Differential Diagnosis, Etologies, Treatment, and References. The third edition is highlighted by a new full-color presentation, more than 240 color illustrations, a DVD with video clips of patients with movement disorders, and tables and figures that encapsulate essential information.
Authoritative coverage that encompasses: Overview and Approach to the Patient; Assessing Disability in Movement Disorders Neuroimaging of Movement Disorders Neuroscientific Foundations Parkinson's Disease Akinetic-Rigid Sydromes Tremor Disorders Dystonic Disorders Choreatic Disorders Myoclonic Disorders; TIC disorders; Ataxias; Wilson's Disease Stiff-Person Syndrome; Gait Disorders; Movement Disorders in Childhood; Restless Legs Syndrome; Movement Disorders Specific to Sleep; Psychogenic Movement Disorders
Neuromuscular Disorders
Rabi Tawil , Shannon Venance
editore: Wiley-Blackwell (an imprint of John Wiley & Sons Ltd)
pagine: 280
A new addition to the Neurology in Practice series, Neuromuscular Disorders provides a clinical guide to the challenging diagnosis and management of neuromuscular disorders. As a part of the series, various feature boxes are highlighted throughout. "Tips and Tricks" give suggestions on how to improve outcomes through practical technique or patient questioning. In addition, "Caution" warning boxes supply helpful advice on how to avoid problems and 'Science Revisited' boxes offer quick reminders of the basic science principles necessary for understanding the presented concepts.
Intrathecal Drug Delivery for Pain and Spasticity
Asokumar Buvanendran
,
Sudhir Diwan
e altri
editore: Saunders
pagine: 224
"Intrathecal Drug Delivery for Pain and Spasticity" - a volume in the new "Interventional and Neuromodulatory Techniques for Pain Management" series - presents state-of-the-art guidance on the full range of intrathecal drug delivery techniques performed today. Asokumar Buvanendran, MD and Sudhir Diwan, M.D., M.S offer expert advice on a variety of procedures to treat chronic non-malignant pain, cancer pain, and spasticity. Comprehensive, evidence-based coverage on selecting and performing these techniques - as well as weighing relative risks and complications - helps you ensure optimum outcomes. With access to the fully searchable text at our associated website, you'll have the detailed visual assistance you need right at your fingertips.
Ataxic Disorders
Alexandra Durr
,
Dick. F. Swaab
e altri
editore: Elsevier Science Ltd
pagine: 680
This volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new neurophysiological and imaging techniques are discussed, along with an in-depth examination of the treatment and management protocols of ataxic diseases. It offers a volume in the "Handbook of Clinical Neurology" series, which has an unparalleled reputation as the world's most comprehensive source of information in neurology. It provides international list of contributors including the leading workers in the field. It describes the advances which have occurred in clinical neurology and the neurosciences, their impact on the understanding of neurological disorders and on patient care.
Clinical Application of Neuromuscular Techniques
The Lower Body
Judith Delany , Leon Chaitow
editore: Churchill Livingstone
pagine: 608
"Clinical Application of Neuromuscular Techniques, Volume 2 - The Lower Body", is a highly illustrated volume of more than 600 pages (Volume 1 - "The Upper Body" is also available). Almost 500 illustrations, with over 400 in two-colours, support the text throughout and make the anatomy and associated techniques easier to understand. This book covers MET (muscle energy techniques), NMT (neuromuscular techniques), PR (positional release) and many other bodywork techniques used in the treatment of neuromusculoskeletal disorders. The text has a regional, joint by joint structure, and the same sequence of headings is used for each joint, making the text easy to dip into. The unique feature of the book is that it describes the normal anatomy and physiology as well as the dysfunctions that may arise, giving a detailed evaluation and description of clinically important aspects of functional anatomy and physiology. Indications for treatments and guidance on making the appropriate treatment choice are given. Palpation methods are evaluated.
The different NMT techniques are then described in relation to the joint anatomy involved, which include not only manual techniques but also acupuncture, hydrotherapies and nutritional support as well as guidance for the patient in the use of self-help approaches. Practical neuromuscular solutions are described in great detail for the treatment of somatic pain and dysfunction together with an eclectic selection of associated manual modalities. This book discusses theories and physiology relevant to the manual treatment of chronic pain, especially as it relates to the soft tissues of the lower body. Step-by-step protocols that address each muscle of a region and a regional approach to treatment are features that make this book unique. A structural review of each region, including ligaments and functional anatomy, adds value for new students and practitioners alike.
Hyperkinetic Movement Disorders
D. F. Swaab
,
Eduardo Tolosa
e altri
editore: Elsevier Science Ltd
pagine: 768
The Handbook of Clinical Neurology Vol 100: Hyperkinetic Movement Disorders discusses hyperkinetic disorders related mainly to basal ganglia dysfunction and pathology. It contains 13 sections and 51 chapters written by authoritative and experienced investigators and clinicians in this extremely broad and diverse group of diseases and syndromes. The first section on choreoathetoid diseases and syndromes includes chapters on Huntington's disease and Huntington's disease look-alikes; spinocerebellar degenerations; neuroacanthocytosis; entatorubral-pallidoluysian atrophy; neuroferritinopathy; neurodegeneration with brain iron accumulation; mitochondrial disorders; acquired hepatocerebral degeneration; benign hereditary chorea; and "senile chorea. The remaining chapters focus on the abnormal involuntary movements associated with each disease or syndrome. These include immune-related chorea, vascular chorea, metabolic disturbances that can induce chorea, chorea in other medical settings (e.g., postpump chorea in children, cancer-related paraneoplastic syndromes), myoclonus, essential tremor, and dystonia, including dystonia plus syndromes.
There are also chapters on tardive dyskinesia, unusual clinical syndromes, and tics and stereotyped movements in children. The text is a valuable resource for neurology and psychiatry residents, practicing neurologists and psychiatrists, and specialists in movement disorders. * An authoritative, comprehensive guide to movement disorders * An invaluable reference for the diagnosis and treatment of hyperkinetic diseases and syndromes * High-level discussions that are ideal for specialists in movement disorders, practitioners and residents alike
Uncommon Causes of Movement Disorders
Nestor Galvez-Jimenez , Paul Tuite
editore: Cambridge
pagine: 346
A large number of neurological conditions result in abnormal movements of the body; these are often characterized by changes in coordination and altered speed of voluntary movement. Many obscure diseases, conditions and environmental insults can cause movement disorders but these are often overlooked. This volume expands and differentiates the many varied clinical presentations of movement disorders. Written by an international team of authors, including some of the most prominent clinicians in the field, disorders are defined and expanded in a clinically useful manner. Pathophysiological theories, genetic discoveries, new classifications, differential diagnoses and therapies are discussed extensively. Uncommon Causes of Movement Disorders provides a broad and comprehensive review of the field, concentrating on conditions infrequently seen but essential for practitioners to recognize in order to implement appropriate management. This is a key text for movement disorders specialists and general neurologists at all stages of their career.
Motor Control
Theories, Experiments, and Applications
Frederic Danion , Mark L. Latash
editore: Oxford University Press Inc
pagine: 536
Motor control has established itself as an area of scientific research characterized by a multi-disciplinary approach. Scientists working in the area of control of voluntary movements come from different backgrounds including but not limited to physiology, physics, psychology, mathematics, neurology, physical therapy, computer science, robotics, and engineering. One of the factors slowing progress in the area has been the lack of communication among researchers representing all these disciplines. A major objective of the curreent book is to overcome this deficiency and to promote cooperation and mutual understanding among researchers addressing different aspects of the complex phenomenon of motor coordination. The book offers a collection of chapters written by the most prominent researchers in the field. Despite the variety of approaches and methods, all the chapters are united by a common goal: To understand how the central nervous system controls and coordinates natural voluntary movements. This book will be appreciated as a major reference by researchers working in all the subfields that form motor control.
It can also be used as a supplementary reading book for graduate courses in such fields as kinesiology, physiology, biomechanics, psychology, robotics, and movement disorders. In one concise volume, Motor Control presents the diversity of the research performed to understand human movement. Deftly organized into 6 primary sections, the editors, Dr Frederic Danion and Dr Mark Latash, have invited the who's who of specialists to write on: MotorControl: Control of a Complex; Cortical Mechanisms of Motor Control; Lessons from Biomechanics; Lessons from Motor Learning and Using Tools; Lessons from Studies of Aging and MotorDisorders; and Lessons from Robotics Motor Control will quickly become the go-to reference for researchers in this growing field. Researchers from mechanics and engineering to psychology and neurophysiology, as well as clinicians working in motor disorders and rehabilitation, will be equally interested in the pages contained herein.
Neuromuscular Disorders: Treatment and Management
Tulio E. Bertorini
editore: Saunders
pagine: 472
"Neuromuscular Disorders" presents a multi-disciplinary approach to the management and therapeutic treatment of the full range of neuromuscular disorders and resulting complications. Dr. Tulio Bertorini and a contributing team of the world's leading authorities in the field provide the latest tools and strategies for minimizing disability and maximizing quality of life. It is in print and online at expertconsult.com.
Movement Disorders
Anthony E. T. Lang
,
Anthony Schapira
e altri
editore: Saunders
pagine: 732
"Movement Disorders 4", the newest volume in the "Blue Books in Neurology" series provides you with rapid access to practical, clinical guidance on the diagnosis and pharmacologic treatment on the full range of movement disorders.
Toole's Cerebrovascular Disorders
E. Steve Roach
,
José Biller
e altri
editore: Cambridge
pagine: 422
Toole's Cerebrovascular Disorders was the first modern book devoted to care of the stroke, originally published more than 40 years ago. This is a completely revised and updated sixth edition of the highly respected standard for stroke diagnosis and treatment. Dr James Toole has stayed on as a consultant for the text, and Drs E. Steve Roach, Kerstin Bettermann, and Jose Biller have reworked Dr Toole's book to include chapters on genetics, pregnancy-related stroke, and acute treatments. The practical focus of the book has not changed, retaining its emphasis on bedside diagnosis and treatment. Easily accessible both for stroke specialists and residents, the sixth edition has been modernized to keep pace with the rapid expansion of knowledge in stroke care and includes evidence-based recommendations, the latest technology and imaging, and risk factors. The text is supplemented with more than 200 images, many in color.
Diagnostic Imaging of Musculoskeletal Diseases
Akbar Bonakdarpour
editore: Humana Press Inc.
pagine: 677
We dedicate this text to Drs. Ernest E. Aegerter, a pathologist, and John A. Kirkpatrick Jr., a radiologist. They were among the principal founders of the ?eld of skeletal pathology and radiology. During their time, their residents and colleagues knew them as great educators with a dedication and a passion for their work. Their textbook, Orthopedic Diseases, published initially in 1958 was among the ?rst interdisciplinary works devoted to this ?eld. Dr. Aegerter and Dr. Kirkpatrick illuminated many aspects of the ?eld of radiology. Today, with the advent of new technologies, this ?eld has grown to include not only diseases that affect the skeleton but also those that affect muscles, ligaments, tendons, and also the cartilaginous structures within joints. With this text we intend to carry on Dr. Aegerter and Dr. Kirkpatrick's tradition. We have recruited only well-known musculoskeletal radiologists and pathologists to participate in the writing of this book. Each author has been carefully selected for his expertise on the topic about which he's been asked to contribute. Each author is known as an experienced and seasoned teacher. Each author has made a mark on the ?eld.
Movement Disorders
An Issue of Neurologic Clinics
Joseph Jankovic
editore: Saunders
Addresses movement disorders. This title contains the following articles: Etiogenesis of Parkinson's Disease; Medical Treatment of Parkinson's Disease; Surgical Treatment of Movement Disorders; Tremor: Clinical Features, Pathophysiology and Treatment; Dystonia - Genetics and Treatment; and, Huntington's Disease and Other Choreas.
The Identification and Treatment of Gait Problems in Cerebral Palsy
James R. Gage
,
Michael H. Schwartz
e altri
editore: Mac Keith Press
pagine: 660
The only book to deal specifically with the treatment of gait problems in cerebral palsy, this comprehensive, multi-disciplinary volume will be invaluable for all those working in the field of cerebral palsy and gait (neurologists, therapists, physiatrists, orthopaedic and neurosurgeons, and bioengineers). The book is divided into two parts. The first is designed to help the reader evaluate and understand a child with cerebral palsy. It deals with neurological control, musculoskeletal growth, and normal gait, as well as cerebral injury, growth deformities and gait pathology in children with cerebral palsy. The second section is a comprehensive overview of management. It emphasizes the most fundamental concept of treatment: manage the child's neurologic dysfunction first and then address the skeletal and muscular consequences of that dysfunction. The book has been thoroughly updated since the previous edition, with a greater focus on treatment and several entirely new topics covered, including chapters on the operative treatment of orthopaedic deformities. The book is accompanied by a DVD containing a teaching video on normal gait and a CD-ROM containing the videos and motion analysis data of all case examples used in the book, as well as teaching videos demonstrating the specifics of many of the procedures used in the correction of gait deformities and gait modelling examples from the Department of Bioengineering at Stanford University.
The Inflammatory Myopathies
Lawrence J. Kagen
editore: Humana Press Inc.
pagine: 356
This book is dedicated to our readers with the intention of providing an informative exposition of the myositis syndromes. It is also presented in the hope that perhaps it may serve to inspire and stimulate discussion and research into these disabling disorders. Included are descriptions of clinical features, differential diagnosis, pathogenetic mechanisms, and approaches to therapy. Current concepts of classi- cation and diagnostic techniques are also presented. The production staff at Humana Springer, especially Ms. F. Louie and Ms. C. Walsh, have been instrumental and invaluable in allowing this work to see the light of day. Above all, the scholarly essays of the contributing authors are acknowledged with gratitude. They have given this volume its character and existence. New York, NY Lawrence J. Kagen v Contents Preface ...v Contributors ...ix 1 Evaluation of the Patient ...1 Lawrence J. Kagen 2 Classification of Idiopathic Inflammatory Myopathies ...15 Frederick W. Miller 3 The Inflammatory Milieu: Cells and Cytokines...29 Ann M. Reed and Thomas A. Griffin 4 Juvenile Dermatomyositis: An Update on Clinical and Laboratory Findings ...55 Lauren M.
Pachman 5 Inclusion Body Myositis ...87 Lawrence J. Kagen 6 The Role of Muscle Biopsy in the Diagnosis of Inflammatory Myopathy ...95 Sakir Humayun Gultekin 7 Electromyography ...1 1 1 Hans L. Carlson 8 Magnetic Resonance Imaging of Myopathies and Myositis ...127 Carolyn M. Sofka 9 Ultrasound in the Evaluation of the Inflammatory Myopathies ...147 Ronald S. Adler and Giovanna Garofalo vii viii Contents 10 Serological Findings ...165 Ira N.
Restless Legs Syndrome
David Rye
,
K. Ray Chaudhuri
e altri
editore: Oxford University Press
pagine: 100
Restless legs syndrome (RLS), also known as Ekbom syndrome, is a common movement disorder with sensorimotor symptoms occurring during sleep and quiet wakefulness. Yoakum described RLS as the "the most common disorder you've never heard of" and this may, unfortunately, be an appropriate description of RLS. The term "restless legs syndrome was first introduced by Karl-Axel Ekbom, a Swedish neurologist and surgeon in 1945. RLS can present in the primary care and secondary care, across a range of specialities such as psychiatry, rheumatology and sleep medicine, and in the UK, the condition remains under-recognised and often regarded as a neurosis in-spite of evidence that RLS adversely affects quality of life. Inappropriate clinical history taking leads to mis-diagnosis and under diagnosis and a sense tat the condition may be a "manufactured" one. Although RLS is effectively treatable and two drugs are now specifically licensed for RLS in the UK, the condition is generally poorly treated and investigated and often prescribed inappropriate drugs.
Patients' descriptions of RLS are wide and varied including "Elvis legs" and an "electric current" running through their legs Because of such a broad, unusual spectrum of reported sensations RLS is frequently misunderstood, and misdiagnosed and even classified as a psychogenic disorder. Patient group surveys in the UK also suggest a consistent delay in diagnosis, delay in referrals and patients often being told "to put up with the symptoms". Part of the Oxford Neurology Library, this pocketbook will highlight the importance of RLS, the ease with RLS can be diagnosed, the problems of misdiagnosis, current thoughts on pathogenesis and the up-to-date treatment. The book will serve as an invaluable quick reference for neurologists, trainees, specialist nurses and general practitioners.
The Behavioral and Cognitive Neurology of Stroke
Julien Bogousslavsky , Olivier Godefroy
editore: Cambridge
pagine: 668
The care of stroke patients has changed dramatically. As well as improvements in the emergency care of the condition, there have been marked advances in our understanding, management and rehabilitation of residual deficits. This book is about the care of stroke patients, focusing on behavioural and cognitive problems. It provides a comprehensive review of the field covering the diagnostic value of these conditions, in the acute and later phases, their requirements in terms of treatment and management and the likelihood and significance of long-term disability. This book will appeal to all clinicians involved in the care of stroke patients, as well as to neuropsychologists, other rehabilitation therapists and research scientists investigating the underlying neuroscience.
