dysimmune neuropathies

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Dysimmune Neuropathies
Author :
Publisher : Academic Press
Release Date :
ISBN 10 : 0128145730
Pages : 266 pages
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Dysimmune Neuropathies provides readers with detailed, basic information that will enable users to recognize and differentiate each neuropathy to adequately guide an investigation and create a treatment plan. An overview of recent progress, avenues for future research, and the desired benefits are also covered. The book highlights the many developments in the field that have occurred in terms of pathophysiological mechanisms, particularly immunological, that have direct implications on treatment strategies. This book is a great reference for trainees, clinicians and researchers specializing in neurology, neuromuscular diseases and neurophysiology. Encompasses all dysimmune neuropathies Describes clinical features, epidemiology, pathophysiology and immunology Provides differential diagnosis Identifies new investigation techniques

Dysimmune Neuropathies

Dysimmune Neuropathies provides readers with detailed, basic information that will enable users to recognize and differentiate each neuropathy to adequately guide an investigation and create a treatment plan. An overview of recent progress, avenues for future research, and the desired benefits are also covered. The book highlights the many developments

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Chronic Dysimmune Neuropathies

Download or read online Chronic Dysimmune Neuropathies written by Mark Ian Busby, published by Unknown which was released on 1999. Get Chronic Dysimmune Neuropathies Books now! Available in PDF, ePub and Kindle.

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Peripheral Nerve Disorders

The identification of autoantibodies associated with dysimmune neuropathies was a major contribution to the characterization of peripheral nerve disorders, the understanding of their pathophysiology, and the clinical diagnosis of neuropathies. Antibodies directed to GM1, GQ1b, and disyalilated gangliosides, and anti-MAG antibodies are very useful in the diagnosis of acute

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Muscle Aging  Inclusion Body Myositis and Myopathies

Muscle weakness with ageing is almost inevitable, generally beginning to manifest beyond the age of 40, and is usually unstoppable. It can lead to reduced mobility, increased risk of falling, injury, and even death. But ?you?re just getting old? is not a sufficient diagnosis. Specific causes of neuromuscular symptoms may

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From Basic Immunology to Immune Mediated Demyelination

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Neurobehavioral Toxicology  Neurological and Neuropsychological Perspectives  Volume II

This book, the second of three volumes, concentrates on peripheral nervous system disorders. Examining the effects of neurotoxicants on nerve, muscle and the neuromuscular junction, it builds on the scientific principles outlined in volume 1 by looking at the application of the methods discussed, particularly in terms of the evaluation and

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The Physiological Basis of Rehabilitation Medicine

The Physiological Basis of Rehabilitation Medicine: Second Edition presents a comprehensive examination of the management of patients with functional impairments due to disease or trauma. It discusses the distinction between disabilities and impairments per se. It addresses the method in which the human body adapts and compensates for the stress

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Essentials of Electrodiagnostic Medicine

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Acquired Neuromuscular Disorders

This book provides state of the art information on the pathogenesis, diagnosis, and treatment of a range of inflammatory, autoimmune, and idiopathic neuromuscular disorders. The opening section discusses the differential diagnosis of acquired myopathies based on clinical, electrophysiological, muscle biopsy, and serological criteria, with special focus on the role of

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Guillain Barre Syndrome

The Guillain-Barre syndrome (GBS) or Landry-Guillain-Barre-Strohl syndrome, also known as post-infectious polyneuropathy or acute idiopathic polyneuritis, is an acute acquired, frequently severe, monophasic autoimmune illness of the peripheral nervous system (PNS). GBS manifests itself with the clinical picture characterised by gait disturbance, pain, weakness, rapidly ascending symmetric flaccid muscle paralysis,

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Cumulated Index Medicus

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DeJong s The Neurologic Examination

Now in its Seventh Edition, DeJong’s The Neurologic Examination has been streamlined and updated for a new generation. An absolutely comprehensive, detailed guide to techniques on the neurologic examination, this book integrates details of neuroanatomy and clinical diagnosis in a readable manner. The text is supplemented by helpful boxes

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Electrodiagnosis in Diseases of Nerve and Muscle

Here is the Fourth Edition of the classic text Electrodiagnosis in Diseases of Nerve and Muscle: Principles and Practice. With each subsequent edition, Dr. Kimura has built upon his extensive experience teaching electromyography (EMG) around the world and has transferred his knowledge to the book. It is intended for clinicians

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