Pathophysiology and treatment of systemic amyloidosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/nrneph.2013.171.pdf
Reference135 articles.
1. Sipe, J. D. et al. Amyloid fibril protein nomenclature: 2010 recommendations from the Nomenclature Committee of the International Society of Amyloidosis. Amyloid 17, 101–104 (2010).
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3. Obici, L., Raimondi, S., Lavatelli, F., Bellotti, V. & Merlini, G. Susceptibility to AA amyloidosis in rheumatic diseases: a critical overview. Arthritis Rheum. 61, 1435–1440 (2009).
4. Saraiva, M. J. Hereditary transthyretin amyloidosis: molecular basis and therapeutical strategies. Exp. Rev. Mol. Med. 4, 1–11 (2002).
5. Cohen, A. S. & Calkins, E. Electron microscopic observations on a fibrous component in amyloid of diverse origins. Nature 183, 1202–1203 (1959).
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