George Karpati
Disorders of Voluntary Muscle
Herausgeber: Hilton-Jones, David; Griggs, Robert C; Bushby, Kate
George Karpati
Disorders of Voluntary Muscle
Herausgeber: Hilton-Jones, David; Griggs, Robert C; Bushby, Kate
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This book provides a resource on the etiology and pathogenesis as well as diagnosis and treatment of diseases of skeletal muscles.
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This book provides a resource on the etiology and pathogenesis as well as diagnosis and treatment of diseases of skeletal muscles.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Produktdetails
- Produktdetails
- Verlag: Cambridge University Press
- 8th edition
- Seitenzahl: 536
- Erscheinungstermin: 26. Februar 2010
- Englisch
- Abmessung: 283mm x 228mm x 37mm
- Gewicht: 2045g
- ISBN-13: 9780521876292
- ISBN-10: 052187629X
- Artikelnr.: 26398806
- Verlag: Cambridge University Press
- 8th edition
- Seitenzahl: 536
- Erscheinungstermin: 26. Februar 2010
- Englisch
- Abmessung: 283mm x 228mm x 37mm
- Gewicht: 2045g
- ISBN-13: 9780521876292
- ISBN-10: 052187629X
- Artikelnr.: 26398806
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.
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.
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.
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.
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.