Hereditary transthyretin amyloidosis: clinical presentation and management updates
C Schwartzlow, M Kazamel - Journal of clinical neuromuscular …, 2020 - journals.lww.com
… Hereditary transthyretin amyloidosis, once a rare progressive … as a result of mutated
transthyretin amyloid aggregation and … to reduce the production of transthyretin and had promising …
transthyretin amyloid aggregation and … to reduce the production of transthyretin and had promising …
Treatment of cardiac transthyretin amyloidosis: an update
M Emdin, A Aimo, C Rapezzi, M Fontana… - European Heart …, 2019 - academic.oup.com
… pharmacological agents that inhibit hepatic synthesis of TTR, stabilize the tetramer, or …
update on this rapidly evolving field, together with practical recommendations on the management …
update on this rapidly evolving field, together with practical recommendations on the management …
Transthyretin cardiac amyloidosis: an update on diagnosis and treatment
H Yamamoto, T Yokochi - ESC heart failure, 2019 - Wiley Online Library
… 11 Management of cardiovascular … TTR in cardiac amyloid deposits after LT,74 suggesting
that paradoxical progressive deposition of wild type TTR on pre-existing variant TTR amyloid …
that paradoxical progressive deposition of wild type TTR on pre-existing variant TTR amyloid …
Transthyretin amyloidosis: update on the clinical spectrum, pathogenesis, and disease-modifying therapies
H Koike, M Katsuno - Neurology and therapy, 2020 - Springer
… the clinical spectrum and management based on the … TTR amyloid deposits [11]. It should
be noted that both cardiomyopathy and carpal tunnel syndrome due to ATTRwt amyloidosis …
be noted that both cardiomyopathy and carpal tunnel syndrome due to ATTRwt amyloidosis …
Evolving landscape in the management of transthyretin amyloidosis
PN Hawkins, Y Ando, A Dispenzeri… - Annals of …, 2015 - Taylor & Francis
… TTR is … However, TTR monomers can undergo a major conformational transformation to
aggregate in a highly ordered and abnormal amyloid fibril form (Citation3); TTR in its amyloid …
aggregate in a highly ordered and abnormal amyloid fibril form (Citation3); TTR in its amyloid …
Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis
A Carroll, PJ Dyck, M de Carvalho… - Journal of Neurology …, 2022 - jnnp.bmj.com
… mutations can be excluded or established on genetic testing, as sequence analysis identifies
>99% of pathogenic variants, with updated lists of TTR mutations and phenotypes reported …
>99% of pathogenic variants, with updated lists of TTR mutations and phenotypes reported …
Management of transthyretin amyloidosis
A Condoluci, M Théaudin… - Swiss medical …, 2021 - research-collection.ethz.ch
… For patients with systemic ATTR amyloidosis, TTR amyloid detection and characterisation in
… Amyloid nomenclature 2020: update and recommendations by the International Society of …
… Amyloid nomenclature 2020: update and recommendations by the International Society of …
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
… At the same time, the development of novel targeted amyloid … to screen asymptomatic
transthyretin amyloidosis gene mutation … advances in treatment for transthyretin amyloidosis‐CA, …
transthyretin amyloidosis gene mutation … advances in treatment for transthyretin amyloidosis‐CA, …
Updates for the diagnosis and management of cardiac amyloidosis
P Gosciniak, T Baron, S Milczarek… - Advances in Clinical …, 2022 - diva-portal.org
… A substantial increase in the interest in transthyretin cardiac amyloidosis (ATTR-CA) is a …
Wildtype transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction…
Wildtype transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction…
Practical recommendations for the diagnosis and management of transthyretin cardiac amyloidosis
V Bistola, J Parissis, E Foukarakis, PN Valsamaki… - Heart Failure …, 2021 - Springer
… light chain amyloidosis (AL) caused by monoclonal immunoglobulin light chains and
transthyretin amyloidosis (ATTR) caused by either mutated or wild-type transthyretin aggregates. …
transthyretin amyloidosis (ATTR) caused by either mutated or wild-type transthyretin aggregates. …
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