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Blood|January 26, 2006
Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in ALGiovanni Palladini, Francesca Lavatelli, Paola Russo, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 15, 2022
Guidelines for non-transplant chemotherapy for treatment of systemic AL amyloidosis: EHA-ISA working groupAshutosh D Wechalekar, M Teresa Cibeira, Simon D Gibbs, et al.
Disease Models & Mechanisms|July 25, 2025
Modeling immunoglobulin light chain amyloidosis in Caenorhabditis elegansMargherita Romeo, Maria Monica Barzago, Alessandro Corbelli, et al.
Annals of Neurology|September 24, 2005
A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathyLaura Obici, Andrea Demarchi, Giulia de Rosa, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|August 19, 2007
A primer of amyloid nomenclaturePer Westermark, Merrill D Benson, Joel N Buxbaum, et al.
Clinical Lymphoma & Myeloma|April 14, 2009
AL amyloidosis associated with IgM monoclonal protein: a distinct clinical entityGiovanni Palladini, Paola Russo, Tiziana Bosoni, et al.
Journal of the American College of Cardiology|November 28, 2015
Diagnosis, Prognosis, and Therapy of Transthyretin AmyloidosisMorie A Gertz, Merrill D Benson, Peter J Dyck, et al.
Blood|February 1, 2015
A practical approach to the diagnosis of systemic amyloidosesCarlos Fernández de Larrea, Laura Verga, Patrizia Morbini, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 26, 2020
Pomalidomide and dexamethasone grant rapid haematologic responses in patients with relapsed and refractory AL amyloidosis: a European retrospective series of 153 patientsPaolo Milani, Faye Sharpley, Stefan O Schönland, et al.
Kidney International|January 8, 2015
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosisGina Gregorini, Claudia Izzi, Pietro Ravani, et al.
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