Muscle aging inclusion-body myositis and myopathies /
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| Format: | Book |
| Language: | English |
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Oxford :
Wiley-Blackwell,
2012.
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| Online Access: | http://site.ebrary.com/lib/ucy/Doc?id=10518751 |
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 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 Dalakas
- Clinical symptoms, physical findings, and diagnostic investigations / Frank Mastaglia
- Pathologic diagnostic criteria of s-IBM and h-IBMS muscle biopsies / Valerie Askanas and W. King Engel
- Function and mutations of the GNE gene leading to DMRV/h-IBM, animal models, and potential treatments / May Malicdan, Satoru Noguchi, Ichizo Nishino
- Clinical and ethnic spectrum, laboratory data, and epidemiology of h-IBM due to GNE mutations / Zohar Argov, Ishizo Nishino, Ikiyo Nonaka
- Consequences of the h-IBM characteristic GNE mutations on muscle proteins in vivo and in vitro / Aldobrando Broccolini and Massimiliano Mirabella
- Function and structure of VCP mutations leading to h-IBM / Cezary Wojcik
- Clinical spectrum, including myopathy, Paget's disease, and fronto-temporal dementia : experimental models of VCP mutations, and potential treatments / Virginia Kimonis
- Animal models of h-IBM due to VCP mutation / Nisha M. Badders and Paul Taylor.