Buch, Englisch, 284 Seiten, Format (B × H): 195 mm x 260 mm, Gewicht: 1010 g
Volume 101
Buch, Englisch, 284 Seiten, Format (B × H): 195 mm x 260 mm, Gewicht: 1010 g
ISBN: 978-0-08-045031-5
Verlag: Elsevier Health Sciences
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.
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
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