Articles
- Inclusion-body myositisClinical, diagnostic, and pathologic aspectsW. King Engel, Valerie Askanas
- Mitochondrial abnormalities in inclusion-body myositisA. Oldfors, A. R. Moslemi, L. Jonasson, M. Ohlsson, G. Kollberg, C. Lindberg
- Amyloidogenic processing of β-amyloid precursor protein in intracellular compartmentsKulandaivelu S. Vetrivel, Gopal Thinakaran
- Common structure and toxic function of amyloid oligomers implies a common mechanism of pathogenesisCharles G. Glabe, Rakez Kayed
- Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathiesF. W. van Leeuwen, P. van Tijn, M.A.F. Sonnemans, B. Hobo, D. M.A. Mann, C. Van Broeckhoven, S. Kumar-Singh, P. Cras, G. Leuba, A. Savioz, M. L.C. Maat-Schieman, H. Yamaguchi, J. M. Kros, W. Kamphorst, E. M. Hol, R. A.I. de Vos, D. F. Fischer
- Preferential degradation of oxidized proteins by the 20S proteasome may be inhibited in aging and in inflammatory neuromuscular diseasesKelvin J.A. Davies, Reshma Shringarpure
- Brain and brawnParallels in oxidative strengthP. I. Moreira, K. Honda, X. Zhu, A. Nunomura, G. Casadesus, M. A. Smith, G. Perry
- The unfolded protein responseA stress signaling pathway critical for health and diseaseKezhong Zhang, Randal J. Kaufman
- Developing therapeutics for the diseases of protein misfoldingBarnaby C.H. May, Cedric Govaerts, Fred E. Cohen
- Pilot trial of etanercept in the treatment of inclusion-body myositisR. J. Barohn, L. Herbelin, J. T. Kissel, W. King, A. L. McVey, D. S. Saperstein, J. R. Mendell
Preface
- Inclusion-body myositisClinical and pathologic aspects, and basic research potentially relevant to treatmentValerie Askanas, Marinos C. Dalakas, W. King Engel
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