… transthyretin amyloidosis outcomes survey: initial report on clinical manifestations in patients
with hereditary and wild-type transthyretin amyloidosis… Hereditary transthyretin amyloidosis: …

… Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection …
Early-onset val30met transthyretin amyloidosis from the transthyretin amyloidosis outcomes survey …

… Hereditary transthyretin amyloidosis (ATTRm amyloidosis) is a rare disease that affects
approximately 1 in every 100,000 individuals [Citation1]. It is one of the most common …

… transthyretin amyloidosis, which includes wild-type (wild-type … Additionally, novel diagnostic
tools like bone scintigraphy … specificity for detecting transthyretin amyloidosis, further aiding …

… features of ATTR amyloidosis, noninvasive diagnosis can be accomplished using nuclear
… Cardiac amyloidosis: evolving diagnosis and management: a scientific statement from the …

… involvement is the most critical part of the diagnosis. Recent advances in imaging techniques
have contributed to the logical diagnostic procedure of determining heart involvement. …

… with left ventricular hypertrophy should lead to consideration of transthyretin amyloidosis. …
and negatives in diphosphonate scintigraphy in the diagnosis of transthyretin amyloidosis. …

… Hereditary transthyretin amyloidosis (ATTRv amyloidosis) is predominantly a disease of
the peripheral nerves, heart, kidney, and eye. CNS involvement has been a marginal issue in …

… Transthyretin amyloidosis with concomitant monoclonal gammopathy of unknown significance
(or any hematological disorder that produces FLC), AL amyloidosis, or coexistence of …

… the amyloid precursor proteins causing a very heterogeneous disease spectrum, but the
main types of amyloidosis involving the heart are light chain (AL) and transthyretin amyloidosis (…