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      Muscular Dystrophies

      AvRobert C. Griggs,Anthony A. Amato

      Inbunden, Engelska, 2011

      Del 101 i serien Handbook of Clinical Neurology

      1 927 kr

      Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

      Beskrivning

      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.



      • Valuable insights into the muscular dystrophies, including treatment, diagnosis, and care and patient management
      • A comprehensive compilation of the combined wisdom of the most highly regarded physicians, experts, and scientists studying the muscular dystrophies
      • An evaluation of the way advances in molecular and cell biology, biochemistry, and other biological sciences continue to advance the study of these disorders

      Produktinformation

      • Utgivningsdatum:2011-05-24
      • Mått:195 x 260 x 20 mm
      • Vikt:1 010 g
      • Format:Inbunden
      • Språk:Engelska
      • Serie:Handbook of Clinical Neurology
      • Antal sidor:284
      • Förlag:Elsevier Science
      • ISBN:9780080450315

      Utforska kategorier

      • Muskuloskeletala sjukdomar inom Medicin

      Mer om författaren

      Dr. Michael J. Aminoff is an internationally recognized, board-certified neurologist and clinical neurophysiologist who works at UCSF Medical Center and specializes in Parkinson's disease and other movement disorders, holding an endowed chair in Parkinson's disease research. Aminoff was educated in England, graduating with honors from University College in London in 1962 and as a physician from University College Hospital Medical School in 1965. He completed postdoctoral training in various London teaching hospitals, but especially at the National Hospital for Neurology and Neurosurgery in Queen Square, London, and at its affiliated Institute of Neurology, where his research on spinal physiology gained him an MD degree (an advanced research thesis in the UK). He joined UCSF Medical Center in 1974, becoming a full professor in 1982; the title of distinguished professor was conferred on him in 2010. In 2000, he was awarded a doctorate in science (an advanced doctorate in the Faculty of Science) from the University of London. He has received numerous awards including the Lifetime Achievement Award from the American Association of Neuromuscular & Electrodiagnostic Medicine (2006) and the A.B.Baker Award from the American Academy of Neurology (2007). He was the editor-in-chief of Muscle and Nerve, a major neuroscience journal for 10 years; serves on the editorial boards of several other medical and scientific journals; and has authored nearly 250 research publications as well as numerous books. Dr. Aminoff is also editor-in-chief of the Encyclopedia of Neurological Sciences and series editor of the multivolume Handbook of Clinical Neurology (Elsevier).

      Innehållsförteckning

      • Chapter 1: Overview of the muscular dystrophiesChapter 2: DystrophinopathiesChapter 3: SarcoglycanopathiesChapter 4: Congenital muscular dystrophiesChapter 5: The collagen VI-related myopathiesChapter 6: Limb-girdle muscular dystrophy 2AChapter 7: DysferlinopathiesChapter 8: Other limb-girdle muscular dystrophiesChapter 9: Limb-girdle muscular dystrophy 2H and the role of TRIM32Chapter 10: CaveolinopathiesChapter 11: Myofibrillar myopathiesChapter 12: Emery–Dreifuss muscular dystrophyChapter 13: Facioscapulohumeral dystrophy and scapuloperoneal syndromesChapter 14: Oculopharyngeal muscular dystrophyChapter 15: Myotonic dystrophy types 1 and 2Chapter 16: Distal muscular dystrophies
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