Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis

A Carroll, PJ Dyck, M de Carvalho… - Journal of Neurology …, 2022 - jnnp.bmj.com
diagnosis is important, given the emergence of effective therapies which have revolutionised
the management of transthyretin amyloidosis. … of diagnostic techniques and management

Practical recommendations for the diagnosis and management of transthyretin cardiac amyloidosis

V Bistola, J Parissis, E Foukarakis, PN Valsamaki… - Heart Failure …, 2021 - Springer
… Most common CA types are light chain amyloidosis (AL) caused by monoclonal immunoglobulin
light chains and transthyretin amyloidosis (ATTR) caused by either mutated or wild-type …

Amyloid transthyretin cardiac amyloidosis: diagnosis and management

B Di Giovanni, D Gustafson… - Expert Review of …, 2019 - Taylor & Francis
… This reaffirms the need for a logical diagnostic algorithm to definitively diagnose and commence
… Refinement of our diagnostic and management techniques will likely help control this …

Management of transthyretin amyloidosis

A Condoluci, M Théaudin… - Swiss medical …, 2021 - research-collection.ethz.ch
Transthyretin amyloidosis (ATTR amyloidosis) is a disease caused by deposition of transthyretin
fibrils in organs and tissues, which causes their dysfunction. The clinical heterogeneity …

Diagnostic and treatment approaches involving transthyretin in amyloidogenic diseases

GY Park, A Jamerlan, KH Shim, SSA An - International journal of …, 2019 - mdpi.com
… The first siRNA-based drug in history to be recently approved by the US FDA for the
treatment of hereditary transthyretin amyloidosis was patisiran, which directly binds to mRNA, …

Recent advances and current dilemmas in the diagnosis and management of transthyretin cardiac amyloidosis

D Addison, JA Slivnick, CM Campbell… - Journal of the …, 2021 - Am Heart Assoc
diagnosis of CA, including the interpretation of indeterminate cardiac imaging findings, the
best technique to screen asymptomatic transthyretin amyloidosis … for transthyretin amyloidosis‐…

Transthyretin cardiac amyloidosis: an update on diagnosis and treatment

H Yamamoto, T Yokochi - ESC heart failure, 2019 - Wiley Online Library
… Thus, it is crucial for clinicians to be aware of this clinical entity for early diagnosis and proper
treatment. In this mini‐review, we focus on recent advances in diagnosis and treatment of …

Current approaches to the diagnosis and management of amyloidosis

MS Taylor, H Sidiqi, J Hare, F Kwok… - Internal Medicine …, 2022 - Wiley Online Library
… developments in amyloidosis diagnosis and management and to provide a diagnostic and
treatment framework to improve the management of patients with all forms of amyloidosis. …

Diagnosis and treatment of hereditary transthyretin amyloidosis (hATTR) polyneuropathy: current perspectives on improving patient care

M Luigetti, A Romano, A Di Paolantonio… - … risk management, 2020 - Taylor & Francis
Hereditary transthyretin amyloidosis (hATTR) with polyneuropathy (formerly known as
Familial Amyloid Polyneuropathy) is a rare disease due to mutations in the gene encoding …

Expert consensus recommendations for the suspicion and diagnosis of transthyretin cardiac amyloidosis

MS Maurer, S Bokhari, T Damy, S Dorbala… - Circulation: Heart …, 2019 - Am Heart Assoc
… imaging is diagnostic of transthyretin amyloidosis with … diagnosing ATTR CA, and
representative scans show diffuse myocardial uptake in a patient with cardiac transthyretin