The "Handbook of Clinical Neurology" (Series Editors: Michael J. Aminoff, Department of Neurology, University of California, San Francisco, USA; FranAois Boller, Bethesda, USA; Dick F. Swaab, Netherlands Institute for Neuroscience, Amsterdam, the Netherlands)has an international reputation as the ultimate reference tool for neurologists involved in clinical research and for neuroscience research workers. It offers comprehensive coverage of the whole field of neurology edited and written by an international list of contributors including the leading workers in the field. This volume is particularly for all those interested in the fundamental aspects of muscle disease or involved with care of patients with these disorders. However, a further separate volume in the Handbook of Clinical Neurology series will be devoted to the muscular dystrophies. The contents include coverage of the latest developments in the subject such as the regulatory nuclear and mitochondrial genetic mechanisms, the proteins involved in muscle function and their remarkable interactions, the nature and function of ion channels and ionic activity, and the complexity of inflammatory cascades that has led to a wider appreciation of the nature of muscle diseases and suggests new approaches for their management. Clinically there has been the recognition and description of new entities and improved classifications of groups of disorders such as the distal myopathies, and the discovery of disease-causing mutation for many of the muscular dystrophies and hereditary myopathies.

Part of the Oxford Textbooks in Clinical Neurology series, the Oxford Textbook of Neuromuscular Disorders covers the scientific basis, clinical diagnosis, and treatment of neuromuscular disorders with a particular focus on the most clinically relevant disorders. The book is organized into seven sections, starting with the general approach to the patient with neuromuscular disorders and then focusing on specific neuromuscular conditions affecting the peripheral nervous system from its origins at the spinal cord anterior horn on its outward course to their effector muscles and the inbound sensory pathways. Chapters on specific neuromuscular conditions are illustrated with typical case histories and their presenting features, allowing readers to put rarer conditions into their clinical context more easily. The concurrent online version allows access to the full content of the textbook, contains links from the references to primary research journal articles, allows full text searches, and provides access to figures and tables that can be downloaded to PowerPoint (R). This textbook will serve as a useful reference for neurologists and specialist trainees in neurology, neuroscientists, neurophysiologists, and other healthcare professionals.

This major new edition fulfils the need for a single-volume, up-to-date information resource on the etiology, pathogenesis, diagnosis and treatment of diseases of skeletal muscles, including the muscular dystrophies, mitochondrial myopathies, metabolic myopathies, ion channel disorders, and dysimmune myopathies. As background to the clinical coverage, relevant information on advances in molecular and developmental biology, immunopathology, mitochondrial biology, ion-channel dynamics, cell membrane and signal transduction science, and imaging technology is summarized. Combining essential new knowledge with the fundamentals of history-taking and clinical examination, this extensively illustrated book will continue to be the mainstay for practising physicians and biomedical scientists concerned with muscle disease. Regular updates on the clinical and basic science aspects of muscle disease - written mainly by rising stars of myology - will be published on an accompanying website.