Disorders of voluntary muscle:
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 dysimmun...
Saved in:
| Other Authors: | |
|---|---|
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Cambridge
Cambridge University Press
2010
|
| Edition: | 8th ed |
| Subjects: | |
| Online Access: | BSB01 FHN01 Volltext |
| Summary: | 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 |
| Item Description: | Title from publisher's bibliographic system (viewed on 05 Oct 2015) |
| Physical Description: | 1 online resource (xvi, 520 pages) |
| ISBN: | 9780511674747 |
| DOI: | 10.1017/CBO9780511674747 |
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| 520 | |a 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 | ||
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| contents | The scientific basis of muscle disease -- Structure and function of muscle fibres and motor units -- Myogenic precursor cells -- Biochemical and molecular basis of muscle disease -- Investigation of muscle Disease -- Electrophysiological evaluation of suspected myopathy -- Histopathology and immunoanalysis of muscle -- Ultrastructural study of muscle -- Diagnostic imaging of muscle -- Description of muscle disease: general aspects -- The clinical assessment and a guide to classification of the myopathies -- The principles of molecular therapies for muscle diseases -- Description of muscle disease: specific diseaes -- Dystrophinopathies -- Muscular dystrophies presenting with proximal muscle weakness -- Dystrophies and myopathies of early childhood onset -- Congenital myopathies -- Muscle diseases with prominent muscle contractures -- Facioscapulohumeral muscular dystrophy -- Distal myopathies -- Oculopharyngeal muscular dystrophy -- Myotonic dystrophy -- Mitochondrial myopathies -- Metabolic myopathies -- Muscle ion channelopathies and related disorders -- Inflammatory myopathies -- Autoimmune and inherited disorders of neuromuscular transmission -- Endocrine and toxic myopathies -- Myofibrillar myopathies -- Hereditary inclusion body myopathies -- Other myopathies |
| ctrlnum | (ZDB-20-CBO)CR9780511674747 (OCoLC)890984055 (DE-599)BVBBV043944347 |
| dewey-full | 616.7/4 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 616 - Diseases |
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| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| doi_str_mv | 10.1017/CBO9780511674747 |
| edition | 8th ed |
| format | Electronic eBook |
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| illustrated | Not Illustrated |
| indexdate | 2024-07-10T07:39:21Z |
| institution | BVB |
| isbn | 9780511674747 |
| language | English |
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| spelling | Disorders of voluntary muscle edited by George Karpati [and others] 8th ed Cambridge Cambridge University Press 2010 1 online resource (xvi, 520 pages) txt rdacontent c rdamedia cr rdacarrier Title from publisher's bibliographic system (viewed on 05 Oct 2015) The scientific basis of muscle disease -- Structure and function of muscle fibres and motor units -- Myogenic precursor cells -- Biochemical and molecular basis of muscle disease -- Investigation of muscle Disease -- Electrophysiological evaluation of suspected myopathy -- Histopathology and immunoanalysis of muscle -- Ultrastructural study of muscle -- Diagnostic imaging of muscle -- Description of muscle disease: general aspects -- The clinical assessment and a guide to classification of the myopathies -- The principles of molecular therapies for muscle diseases -- Description of muscle disease: specific diseaes -- Dystrophinopathies -- Muscular dystrophies presenting with proximal muscle weakness -- Dystrophies and myopathies of early childhood onset -- Congenital myopathies -- Muscle diseases with prominent muscle contractures -- Facioscapulohumeral muscular dystrophy -- Distal myopathies -- Oculopharyngeal muscular dystrophy -- Myotonic dystrophy -- Mitochondrial myopathies -- Metabolic myopathies -- Muscle ion channelopathies and related disorders -- Inflammatory myopathies -- Autoimmune and inherited disorders of neuromuscular transmission -- Endocrine and toxic myopathies -- Myofibrillar myopathies -- Hereditary inclusion body myopathies -- Other myopathies 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 Muscles / Diseases Neuromuskuläre Krankheit (DE-588)4075332-3 gnd rswk-swf Neuromuskuläre Krankheit (DE-588)4075332-3 s 1\p DE-604 Karpati, George edt Erscheint auch als Druckausgabe 978-0-521-87629-2 https://doi.org/10.1017/CBO9780511674747 Verlag URL des Erstveröffentlichers Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Disorders of voluntary muscle The scientific basis of muscle disease -- Structure and function of muscle fibres and motor units -- Myogenic precursor cells -- Biochemical and molecular basis of muscle disease -- Investigation of muscle Disease -- Electrophysiological evaluation of suspected myopathy -- Histopathology and immunoanalysis of muscle -- Ultrastructural study of muscle -- Diagnostic imaging of muscle -- Description of muscle disease: general aspects -- The clinical assessment and a guide to classification of the myopathies -- The principles of molecular therapies for muscle diseases -- Description of muscle disease: specific diseaes -- Dystrophinopathies -- Muscular dystrophies presenting with proximal muscle weakness -- Dystrophies and myopathies of early childhood onset -- Congenital myopathies -- Muscle diseases with prominent muscle contractures -- Facioscapulohumeral muscular dystrophy -- Distal myopathies -- Oculopharyngeal muscular dystrophy -- Myotonic dystrophy -- Mitochondrial myopathies -- Metabolic myopathies -- Muscle ion channelopathies and related disorders -- Inflammatory myopathies -- Autoimmune and inherited disorders of neuromuscular transmission -- Endocrine and toxic myopathies -- Myofibrillar myopathies -- Hereditary inclusion body myopathies -- Other myopathies Muscles / Diseases Neuromuskuläre Krankheit (DE-588)4075332-3 gnd |
| subject_GND | (DE-588)4075332-3 |
| title | Disorders of voluntary muscle |
| title_auth | Disorders of voluntary muscle |
| title_exact_search | Disorders of voluntary muscle |
| title_full | Disorders of voluntary muscle edited by George Karpati [and others] |
| title_fullStr | Disorders of voluntary muscle edited by George Karpati [and others] |
| title_full_unstemmed | Disorders of voluntary muscle edited by George Karpati [and others] |
| title_short | Disorders of voluntary muscle |
| title_sort | disorders of voluntary muscle |
| topic | Muscles / Diseases Neuromuskuläre Krankheit (DE-588)4075332-3 gnd |
| topic_facet | Muscles / Diseases Neuromuskuläre Krankheit |
| url | https://doi.org/10.1017/CBO9780511674747 |
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