Recent advances in the management of AL Amyloidosis
Author:
Affiliation:
1. Department of Clinical Therapeutics; National and Kapodistrian University of Athens; School of Medicine; Athens Greece
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.13805/fullpdf
Reference105 articles.
1. Functional gene expression analysis of clonal plasma cells identifies a unique molecular profile for light chain amyloidosis;Abraham;Blood,2005
2. Hyperdiploidy is less frequent in AL amyloidosis compared with monoclonal gammopathy of undetermined significance and inversely associated with translocation t(11;14);Bochtler;Blood,2011
3. Gain of chromosome 1q21 is an independent adverse prognostic factor in light chain amyloidosis patients treated with melphalan/dexamethasone;Bochtler;Amyloid,2014
4. Translocation t(11;14) is associated with adverse outcome in patients with newly diagnosed AL amyloidosis when treated with bortezomib-based regimens;Bochtler;Journal of Clinical Oncology,2015
5. Antibodies to human serum amyloid P component eliminate visceral amyloid deposits;Bodin;Nature,2010
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