Cardiac Amyloidosis Therapy: A Systematic Review

Heart involvement in Cardiac Amyloidosis (CA) results in a worsening of the prognosis in almost all patients with both light-chain (AL) and transthyretin amyloidosis (ATTR). The mainstream CA is a restrictive cardiomyopathy with hypertrophic phenotype at cardiac imaging that clinically leads to hear...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Franco Iodice [verfasserIn] Marco Di Mauro [verfasserIn] Marco Giuseppe Migliaccio [verfasserIn] Angela Iannuzzi [verfasserIn] Roberta Pacileo [verfasserIn] Martina Caiazza [verfasserIn] Augusto Esposito [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	cardiac amyloidosis therapies amyloidosis

Übergeordnetes Werk:	In: Cardiogenetics - MDPI AG, 2011, 11(2021), 1, Seite 10-17
Übergeordnetes Werk:	volume:11 ; year:2021 ; number:1 ; pages:10-17

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.3390/cardiogenetics11010002

Katalog-ID:	DOAJ050254189

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language	English
source	In Cardiogenetics 11(2021), 1, Seite 10-17 volume:11 year:2021 number:1 pages:10-17
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authorswithroles_txt_mv	Franco Iodice @@aut@@ Marco Di Mauro @@aut@@ Marco Giuseppe Migliaccio @@aut@@ Angela Iannuzzi @@aut@@ Roberta Pacileo @@aut@@ Martina Caiazza @@aut@@ Augusto Esposito @@aut@@
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author	Franco Iodice
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topic_title	RC666-701 Cardiac Amyloidosis Therapy: A Systematic Review cardiac amyloidosis therapies amyloidosis
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topic_unstemmed	misc RC666-701 misc cardiac amyloidosis misc therapies amyloidosis misc Diseases of the circulatory (Cardiovascular) system
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title	Cardiac Amyloidosis Therapy: A Systematic Review
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title_full	Cardiac Amyloidosis Therapy: A Systematic Review
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author_browse	Franco Iodice Marco Di Mauro Marco Giuseppe Migliaccio Angela Iannuzzi Roberta Pacileo Martina Caiazza Augusto Esposito
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title_sort	cardiac amyloidosis therapy: a systematic review
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title_auth	Cardiac Amyloidosis Therapy: A Systematic Review
abstract	Heart involvement in Cardiac Amyloidosis (CA) results in a worsening of the prognosis in almost all patients with both light-chain (AL) and transthyretin amyloidosis (ATTR). The mainstream CA is a restrictive cardiomyopathy with hypertrophic phenotype at cardiac imaging that clinically leads to heart failure with preserved ejection fraction (HFpEF). An early diagnosis is essential to reduce cardiac damage and to improve the prognosis. Many therapies are available, but most of them have late benefits to cardiac function; for this reason, novel therapies are going to come soon.
abstractGer	Heart involvement in Cardiac Amyloidosis (CA) results in a worsening of the prognosis in almost all patients with both light-chain (AL) and transthyretin amyloidosis (ATTR). The mainstream CA is a restrictive cardiomyopathy with hypertrophic phenotype at cardiac imaging that clinically leads to heart failure with preserved ejection fraction (HFpEF). An early diagnosis is essential to reduce cardiac damage and to improve the prognosis. Many therapies are available, but most of them have late benefits to cardiac function; for this reason, novel therapies are going to come soon.
abstract_unstemmed	Heart involvement in Cardiac Amyloidosis (CA) results in a worsening of the prognosis in almost all patients with both light-chain (AL) and transthyretin amyloidosis (ATTR). The mainstream CA is a restrictive cardiomyopathy with hypertrophic phenotype at cardiac imaging that clinically leads to heart failure with preserved ejection fraction (HFpEF). An early diagnosis is essential to reduce cardiac damage and to improve the prognosis. Many therapies are available, but most of them have late benefits to cardiac function; for this reason, novel therapies are going to come soon.
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title_short	Cardiac Amyloidosis Therapy: A Systematic Review
url	https://doi.org/10.3390/cardiogenetics11010002 https://doaj.org/article/c5b40b8f444c48a98585bf141cc68f63 https://www.mdpi.com/2035-8148/11/1/2 https://doaj.org/toc/2035-8253 https://doaj.org/toc/2035-8148
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up_date	2024-07-03T13:51:34.546Z
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