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Informationen zum Autor 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. Klappentext This book provides a resource on the etiology and pathogenesis as well as diagnosis and treatment of diseases of skeletal muscles. Zusammenfassung This major new edition fulfils the need for a single-volume! up-to-date information resource on the etiology and pathogenesis as well as diagnosis and treatment of diseases of skeletal muscles. It is the trusted and respected authority on muscle disease. Inhaltsverzeichnis 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. Bönnemann and Enrico Bertini; 13. Congenital myopathies Carina Wallgren-Pettersson and Nigel G. Laing; 14. Muscle diseases with prominent muscle contractures Gisèle 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 Lochmüller 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....
