Disorders of Voluntary Muscle
8th Edition
Published on 2. March 2010
978-0-511-66940-8 (ISBN)
Description
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.
Reviews / Votes
'After reading through the text, one will achieve a solid foundation in clinical myology. This book will be useful for any clinician who diagnoses and manages patients with muscle disease, and for students, residents, and fellows with an interest in such.' Mark B. Bromberg, MD, PhD, NeurologyMore details
Edition
8th Revised edition
Language
English
Place of publication
Cambridge
United Kingdom
Publishing group
Cambridge University Press
Target group
Professional and scholarly
Edition type
Revised edition
Illustrations
69 Tables, unspecified; 140 Halftones, unspecified
File size
20,00 MB
ISBN-13
978-0-511-66940-8 (9780511669408)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
George Karpati | David Hilton-Jones | Kate Bushby
Disorders of Voluntary Muscle
Book
01/2010
8th Edition
Cambridge University Press
€461.50
No shipping information available
Persons
George Karpati is Isaac Walton Killam Chair and Professor at the Department of Neurology and Neurosurgery, McGill University, and the Montreal Neurological Institute, Montreal, Quebec, Canada. David Hilton-Jones is Clinical Director of the Muscular Dystrophy Campaign Muscle and Nerve Centre, John Radcliffe Hospital, Oxford, UK. Kate Bushby is Professor of Neuromuscular Genetics at the Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK. Robert C. Griggs is Professor of Neurology, Medicine, Pediatrics, Pathology and Laboratory Medicine at the Department of Neurology, University of Rochester School of Medicine and Dentistry and Strong Memorial Hospital, Rochester, New York, USA. He is also Chair of the Muscle Study Group Executive Committee.
Content
Preface; Foreword John Walton; Part I. The Scientific Basis of Muscle Disease: 1. Structure and function of muscle fibres and motor units Mary Kay Floeter; 2. Myogenic precursor cells Miranda D. Grounds and Frederic Relaix; 3. Biochemical and molecular basis of muscle disease Susan Brown and Cecilia Jimenez-Mallebera; Part II. Investigation of Muscle Disease: 4. Electromyography and related techniques Eric Logigian and Emma Ciafaloni; 5. Histopathology and immunoanalysis of muscle Caroline A. Sewry and Maria J. Molnar; 6. Ultrastructural study of muscle Anders Oldfors; 7. Diagnostic imaging of muscle Eugenio Mercuri and Marianne de Visser; Part III. Description of Muscle Disease; Section 1. General Aspects: 8. The clinical assessment and a guide to classification of the myopathies David Hilton-Jones and John T. Kissel; 9. The principles of molecular therapies for muscle diseases George Karpati and Renald Gilbert; Section 2. Specific Diseases: 10. Dystrophinopathies Michael Sinnreich; 11. Muscular dystrophies presenting with proximal muscle weakness Mariz Vainzof and Kate Bushby; 12. Dystrophies and myopathies of early childhood onset Carsten G. Boennemann and Enrico Bertini; 13. Congenital myopathies Carina Wallgren-Pettersson and Nigel G. Laing; 14. Muscle diseases with prominent muscle contractures Gisele Bonne and Anne K. Lampe; 15. Facioscapulohumeral muscular dystrophy Shannon L. Venance and Rabi Tawil; 16. Distal myopathies Bjarne Udd; 17. Oculopharyngeal muscular dystrophy Bernard Brais; 18. Myotonic dystrophy John Day and Charles Thornton; 19. Mitochondrial myopathies and related disorders Patrick F. Chinnery and Eric A. Shoubridge; 20. Metabolic myopathies John Vissing, Stefano DiDonato and Franco Taroni; 21. Muscle ion channelopathies and related disorders Bertrand Fontaine and Michael G. Hanna; 22. Inflammatory and dysimmune myopathies Marinos C. Dalakas and George Karpati; 23. Myasthenia gravis and myasthenic syndromes [autoimmune and genetic] Amelia Evoli, Hanns Lochmueller and Violeta Mihaylova; 24. Endocrine and toxic myopathies Zohar Argov and Frank L. Mastaglia; 25. Myofibrillar myopathy Duygu Selcen; 26. Hereditary inclusion body myopathies Zohar Argov and Stella Mitrani-Rosenbaum; 27. Other myopathies Giovanni Meola and Michael Swash.
