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" Muscle aging : "
edited by Valerie Askanas and W. King Engel
Document Type
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BL
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Record Number
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589382
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Doc. No
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b418601
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Title & Author
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Muscle aging : : inclusion-body myositis and myopathies /\ edited by Valerie Askanas and W. King Engel
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Publication Statement
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Chichester, West Sussex :: Wiley-Blackwell,, 2012
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Page. NO
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xii, 250 p., [8] p. of col. plates :: ill. ;; 26 cm
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ISBN
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9781405196468 (hardcover : alk. paper)
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: 1405196467
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Bibliographies/Indexes
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Includes bibliographical references and index
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Contents
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Ageing of the human neuromuscular system : pathological aspects / W. King Engel and Valerie Askanas -- Aging of the human neuromuscular system : clinical considerations / W. King Engel and Valerie Askanas -- Aging of the human neuromuscular system : patient vignettes / W. King Engel, Shalini Mahajan, Valerie Askanas -- Mitochondrial changes in ageing with particular reference to muscle, and possible clinical consequences / Salvatore DiMauro, Eric Schon, Michio Hirano -- Protein degradation in ageing cells and mitochondria : relevance to the neuromuscular system / Jenny Ngo and Kelvin J. A. Davies -- Human muscle protein metabolism in relation to exercise and aging : potential therapeutic applications / Micah J. Drummond, Blake B. Rasmussen -- Pathogenesis of sporadic inclusion-body myositis / Valerie Askanas, W. King Engel, Anna Nogalska -- Inflammatory and autoimmune features of inclusion-body myositis / Marinos C. Dalakas -- Sporadic inclusion-body myositis: clinical symptoms, physical findings, and diagnostic investigations / Frank L. Mastaglia -- Pathologic diagnostic criteria of sporadic inclusion-body myositis and hereditary inclusion-body myopathy muscle biopsies / Valerie Askanas and W. King Engel -- Function and mutations of the GNE gene leading to distal myopathy with rimmed vacuoles hereditary inclusion-body myopathy, animal models, and potential treatments / May Christine V. Malicdan, Satoru Noguchi, Ichizo Nishino -- GNE myopathy (hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles): clinical features and epidemiology / Zohar Argov, Ishizo Nishino, Ikiyo Nonaka -- Consequences of the hereditary inclusion-body myopathy-characteristic GNE mutations on muscle proteins in vivo and in vitro / Aldobrando Broccolini and Massimiliano Mirabella -- Function and structure of VCP mutations leading to inclusion-body myopathy associated with Paget disease of bone and frontotemporal dementia / Cezary Wojcik -- Clinical spectrum of VCP myopathy, Paget disease, and frontotemporal dementia : experimental models and potential treatments / Virginia Kimonis ...[et al] -- Drosophila and mouse models of hereditary myopathy caused by mutations in VCP / Nisha M. Badders and J. Paul Taylor
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Subject
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Myositis
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Subject
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Myositis, Inclusion Body-- physiopathology
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Subject
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Aging
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Dewey Classification
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612.3
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LC Classification
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RC935.M9M87 2012
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NLM classification
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2012 D-419
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WE 544
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Added Entry
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Askanas, Valerie
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Engel, W. King
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