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Blood|July 17, 2014
Treatment recommendations for patients with Waldenström macroglobulinemia (WM) and related disorders: IWWM-7 consensusMeletios A Dimopoulos, Efstathios Kastritis, Roger G Owen, et al.
British Journal of Haematology|November 16, 2012
Response assessment in Waldenström macroglobulinaemia: update from the VIth International WorkshopRoger G Owen, Robert A Kyle, Marvin J Stone, et al.
Circulation. Heart Failure|June 15, 2017
Design and Rationale of the Phase 3 ATTR-ACT Clinical Trial (Tafamidis in Transthyretin Cardiomyopathy Clinical Trial)Mathew S Maurer, Perry Elliott, Giampaolo Merlini, et al.
Gastroenterology|May 8, 2004
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian familiesLaura Obici, Giovanni Palladini, Sofia Giorgetti, et al.
American Journal of Hematology|December 4, 2024
Feasibility of a Biomarker-Based Screening for Pre-Symptomatic AL Amyloidosis in Patients With Intermediate/High-Risk MGUSSilvia Mangiacavalli, Paolo Milani, Claudio Salvatore Cartia, et al.
Nature Communications|March 22, 2019
Cryo-EM structure of cardiac amyloid fibrils from an immunoglobulin light chain AL amyloidosis patientPaolo Swuec, Francesca Lavatelli, Masayoshi Tasaki, et al.
Leukemia Research|April 28, 2009
SDF1/CXCL12 (-801GA) polymorphism is a prognostic factor after treatment initiation in Waldenstrom macroglobulinemiaStéphanie Poulain, Marjan Ertault, Xavier Leleu, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 12, 2010
Embryonic stem and haematopoietic progenitor cells resist to Aβ oligomer toxicity and maintain the differentiation potency in cultureTui Neri, Monica Bucciantini, Vittorio Rosti, et al.
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