Light Chain (AL) Amyloidosis: The Journey to Diagnosis-Reference-Cited by-同舟云学术

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Light Chain (AL) Amyloidosis: The Journey to Diagnosis

Published:2017-08-14 Issue:2 Volume:11 Page:207-216
ISSN:1178-1653
Container-title:The Patient - Patient-Centered Outcomes Research
language:en
Short-container-title:Patient

Author:

McCausland Kristen L.,White Michelle K.,Guthrie Spencer D.,Quock Tiffany,Finkel Muriel,Lousada Isabelle,Bayliss Martha S.

Funder

Prothena Biosciences, Inc

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/article/10.1007/s40271-017-0273-5/fulltext.html

Reference14 articles.

1. Kyle RA, Linos A, Beard CM, Linke RP, Gertz MA, O’Fallon WM, et al. Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. Blood. 1992;79(7):1817–22.

2. Pinney JH, Smith CJ, Taube JB, Lachmann HJ, Venner CP, Gibbs SD, et al. Systemic amyloidosis in England: an epidemiological study. Br J Haematol. 2013;161(4):525–32.

3. Falk RH, Comenzo RL, Skinner M. The systemic amyloidoses. N Engl J Med. 1997;337(13):898–909.

4. Merlini G, Seldin DC, Gertz MA. Amyloidosis: pathogenesis and new therapeutic options. J Clin Oncol. 2011;29(14):1924–33.

5. Palladini G, Lavatelli F, Russo P, Perlini S, Perfetti V, Bosoni T, et al. Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in AL. Blood. 2006;107(10):3854–8.

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