Management of AL amyloidosis in 2020

G Palladini, P Milani, G Merlini - Blood, The Journal of the …, 2020 - ashpublications.org
In amyloid light chain (AL) amyloidosis, a small B-cell clone, most commonly a plasma cell
clone, produces monoclonal light chains that exert organ toxicity and deposit in tissue in the …

Systemic amyloidosis from A (AA) to T (ATTR): a review

E Muchtar, A Dispenzieri, H Magen… - Journal of internal …, 2021 - Wiley Online Library
Systemic amyloidosis is a rare protein misfolding and deposition disorder leading to
progressive organ failure. There are over 15 types of systemic amyloidosis, each caused by …

[HTML][HTML] Patisiran treatment in patients with transthyretin cardiac amyloidosis

MS Maurer, P Kale, M Fontana, JL Berk… - … England Journal of …, 2023 - Mass Medical Soc
Background Transthyretin amyloidosis, also called ATTR amyloidosis, is associated with
accumulation of ATTR amyloid deposits in the heart and commonly manifests as progressive …

Daratumumab-based treatment for immunoglobulin light-chain amyloidosis

E Kastritis, G Palladini, MC Minnema… - … England Journal of …, 2021 - Mass Medical Soc
Background Systemic immunoglobulin light-chain (AL) amyloidosis is characterized by
deposition of amyloid fibrils of light chains produced by clonal CD38+ plasma cells …

Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases

P Garcia-Pavia, C Rapezzi, Y Adler, M Arad… - European heart …, 2021 - academic.oup.com
Cardiac amyloidosis is a serious and progressive infiltrative disease that is caused by the
deposition of amyloid fibrils at the cardiac level. It can be due to rare genetic variants in the …

Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D …

P Garcia‐Pavia, C Rapezzi, Y Adler… - European journal of …, 2021 - Wiley Online Library
Cardiac amyloidosis is a serious and progressive infiltrative disease that is caused by the
deposition of amyloid fibrils at the cardiac level. It can be due to rare genetic variants in the …

CRISPR-Cas9 gene editing with nexiguran ziclumeran for ATTR cardiomyopathy

M Fontana, SD Solomon, J Kachadourian… - … England Journal of …, 2024 - Mass Medical Soc
Background Transthyretin amyloidosis with cardiomyopathy (ATTR-CM) is a progressive,
often fatal disease. Nexiguran ziclumeran (nex-z) is an investigational therapy based on …

Systemic immunoglobulin light chain amyloidosis

G Merlini, A Dispenzieri, V Sanchorawala… - Nature reviews Disease …, 2018 - nature.com
Systemic immunoglobulin light chain amyloidosis is a protein misfolding disease caused by
the conversion of immunoglobulin light chains from their soluble functional states into highly …

The evaluation of monoclonal gammopathy of renal significance: a consensus report of the International Kidney and Monoclonal Gammopathy Research Group

N Leung, F Bridoux, V Batuman, A Chaidos… - Nature Reviews …, 2019 - nature.com
The term monoclonal gammopathy of renal significance (MGRS) was introduced by the
International Kidney and Monoclonal Gammopathy Research Group (IKMG) in 2012. The …

Systemic amyloidosis

AD Wechalekar, JD Gillmore, PN Hawkins - The Lancet, 2016 - thelancet.com
Tissue deposition of protein fibrils causes a group of rare diseases called systemic
amyloidoses. This Seminar focuses on changes in their epidemiology, the current approach …