Muscle aging : inclusion-body myositis and myopathies /
For neurologists, neuroscientists, gerontologists, internists, general physicians, nurses, and physical therapists, Askanas and Engel (neurology and pathology, U. of Southern California) compile 16 articles on muscle aging and sporadic inclusion-body myositis, as well as hereditary inclusion-body my...
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| Format: | Book |
| Language: | English |
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Chichester, West Sussex :
Wiley-Blackwell,
2012
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Table of Contents:
- 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