Muscular dystrophies
著者
書誌事項
Muscular dystrophies
（Handbook of clinical neurology, 101）
Elsevier, 2011
- : hardcover
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注記
Includes bibliographical references and index
内容説明・目次
内容説明
The Handbook of Clinical Neurology Vol 101: Muscular Dystrophies discusses the pathogenesis and treatment prospects for muscular dystrophies. It summarizes the advances in molecular and cell biology, biochemistry, and other biological sciences, with an emphasis on their application to this group of muscle disorders and to their clinical implications.
Starting with an overview of muscular dystrophies, the book's 16 chapters discuss dystrophinopathies; sarcoglycanopathies; congenital muscular dystrophies; collagen VI-related myopathies; limb-girdle muscular dystrophy 2A; dysferlinopathies; limb-girdle muscular dystrophy 2H and the role of TRIM32; and caveolinopathies. The book also covers myofibrillar myopathies; Emery-Dreifuss muscular dystrophy; facioscapulohumeral dystrophy and scapuloperoneal syndromes; oculopharyngeal muscular dystrophy; myotonic dystrophy types 1 and 2; and distal muscular dystrophies.
This book is useful to basic investigators, as it offers an increased understanding of muscular dystrophies; and to clinicians, with its emphasis on issues that are relevant to the care, diagnosis, and management of patients with these disorders.
目次
Chapter 1: Overview of the muscular dystrophies
Chapter 2: Dystrophinopathies
Chapter 3: Sarcoglycanopathies
Chapter 4: Congenital muscular dystrophies
Chapter 5: The collagen VI-related myopathies
Chapter 6: Limb-girdle muscular dystrophy 2A
Chapter 7: Dysferlinopathies
Chapter 8: Other limb-girdle muscular dystrophies
Chapter 9: Limb-girdle muscular dystrophy 2H and the role of TRIM32
Chapter 10: Caveolinopathies
Chapter 11: Myofibrillar myopathies
Chapter 12: Emery-Dreifuss muscular dystrophy
Chapter 13: Facioscapulohumeral dystrophy and scapuloperoneal syndromes
Chapter 14: Oculopharyngeal muscular dystrophy
Chapter 15: Myotonic dystrophy types 1 and 2
Chapter 16: Distal muscular dystrophies
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