Impact of Delayed Diagnosis and Misdiagnosis for Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM): A Targeted Literature Review
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2193-6544
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Impact of Delayed Diagnosis and Misdiagnosis for Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM): A Targeted Literature Review ; volume:10 ; number:1 ; day:20 ; month:4 ; year:2021 ; pages:141-159 ; date:6.2021
Cardiology and therapy ; 10, Heft 1 (20.4.2021), 141-159, 6.2021
- Creator
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Rozenbaum, Mark H.
Large, Samuel
Bhambri, Rahul
Stewart, Michelle
Whelan, Jo
Doornewaard, Alexander van
Dasgupta, Noel
Masri, Ahmad
Nativi-Nicolau, Jose
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s40119-021-00219-5
- URN
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urn:nbn:de:101:1-2021091618562297484900
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Rozenbaum, Mark H.
- Large, Samuel
- Bhambri, Rahul
- Stewart, Michelle
- Whelan, Jo
- Doornewaard, Alexander van
- Dasgupta, Noel
- Masri, Ahmad
- Nativi-Nicolau, Jose
- SpringerLink (Online service)
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Transthyretin amyloid cardiomyopathy in women: frequency, characteristics, and diagnostic challenges
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Transthyretin amyloid cardiomyopathy in patients with unexplained increased left ventricular wall thickness
Treatment of transthyretin (TTR) amyloid cardiomyopathy with an antisense oligonucleotide inhibitor of TTR synthesis
Annual Cardiovascular-Related Hospitalization Days Avoided with Tafamidis in Patients with Transthyretin Amyloid Cardiomyopathy
Estimating the Prevalence of Transthyretin Amyloid Cardiomyopathy in a Large In-Hospital Database in Japan
Multi-modality artificial intelligence-based transthyretin amyloid cardiomyopathy detection in patients with severe aortic stenosis
Diagnosis of Transthyretin Amyloid Cardiomyopathy
Transthyretin Amyloid Cardiomyopathy in a Young Female
Assessment of transthyretin instability in patients with wild-type transthyretin amyloid cardiomyopathy
Transthyretin amyloid cardiomyopathy in women: frequency, characteristics, and diagnostic challenges
Molecular mechanisms and emerging therapies in wild-type transthyretin amyloid cardiomyopathy
Extrapolation of Survival Benefits in Patients with Transthyretin Amyloid Cardiomyopathy Receiving Tafamidis: Analysis of the Tafamidis in Transthyretin Cardiomyopathy Clinical Trial
Clinical characteristics and prognosis of Chinese patients with hereditary transthyretin amyloid cardiomyopathy
Transthyretin amyloid cardiomyopathy in patients with unexplained increased left ventricular wall thickness
Treatment of transthyretin (TTR) amyloid cardiomyopathy with an antisense oligonucleotide inhibitor of TTR synthesis
Annual Cardiovascular-Related Hospitalization Days Avoided with Tafamidis in Patients with Transthyretin Amyloid Cardiomyopathy
Estimating the Prevalence of Transthyretin Amyloid Cardiomyopathy in a Large In-Hospital Database in Japan