PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Muscle Aging, Inclusion‐Body Myositis and Myopathies10.1002/9781444398311.ch102011168-174Pathologic Diagnostic Criteria of Sporadic Inclusion‐Bodyc Myositis and Hereditary Inclusion‐Body Myopathy Muscle BiopsiesValerie Askanas, W. King Engelhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch10, https://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch10
Muscle Aging, Inclusion‐Body Myositis and Myopathies10.1002/9781444398311.ch92011159-167Sporadic Inclusion‐Body Myositis: Clinical Symptoms, Physical Findings, and Diagnostic InvestigationsFrank L. Mastagliahttps://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch9, https://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch9
Gerontology10.1159/0004947232019653240-252Resistance Exercise Improves Mitochondrial Quality Control in a Rat Model of Sporadic Inclusion Body MyositisJung-Hoon Koo, Eun-Bum Kang, Joon-Yong Chohttps://www.karger.com/Article/Pdf/494723, https://www.karger.com/Article/Pdf/494723
Journal of Neurochemistry10.1111/j.1471-4159.2006.03668.x20069651491-1499Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced cultured human muscle fibersAnna Nogalska, W. King Engel, Janis McFerrin, Koichi Kokame, Hiroto Komano, Valerie Askanashttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1471-4159.2006.03668.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.2006.03668.x/fullpdf
Neuropathology and Applied Neurobiology10.1111/nan.120382013397750-761Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibresM. Cacciottolo, A. Nogalska, C. D'Agostino, W. K. Engel, V. Askanashttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fnan.12038
Occupational Therapy International10.1002/oti.13252012192108-116Hand Function in 45 Patients with Sporadic Inclusion Body MyositisMarianne Eriksson, Christopher Lindberghttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Foti.1325, https://onlinelibrary.wiley.com/doi/full/10.1002/oti.1325
Muscle Aging, Inclusion‐Body Myositis and Myopathies10.1002/9781444398311.ch72011109-145Pathogenesis of Sporadic Inclusion‐Body Myositis: Role of Aging and Muscle‐Fiber Degeneration, and Accumulation of the Same Proteins as in Alzheimer and Parkinson BrainsValerie Askanas, W. King Engel, Anna Nogalskahttps://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch7, https://onlinelibrary.wiley.com/doi/pdf/10.1002/9781444398311.ch7
Clinical Physiology and Functional Imaging10.1111/cpf.122592015366504-509Effects of blood-flow-restricted resistance training on muscle function in a 74-year-old male with sporadic inclusion body myositis: a case reportA. N. Jørgensen, P. Aagaard, J. L. Nielsen, U. Frandsen, L. P. Diederichsenhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcpf.12259
European Journal of Applied Physiology10.1007/s0042100503471998774372-378Adaptations in rat skeletal muscle following long-term resistance exercise trainingNoel D. Duncan, David A. Williams, Gordon S. Lynchhttp://link.springer.com/content/pdf/10.1007/s004210050347.pdf, http://link.springer.com/article/10.1007/s004210050347/fulltext.html, http://link.springer.com/content/pdf/10.1007/s004210050347
Muscle & Nerve10.1002/mus.238982013492175-180Invasive fibroblasts: Fundamental difference between sporadic inclusion body myositis and polymyositisKathrin Doppler, Georgios Pantazis, Alfred Lindner, Andreas Mack, Antje Bornemannhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmus.23898, https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmus.23898, http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.23898/fullpdf