Transthyretin amyloidosis prevalence and characteristics in Korean patients with heart failure with preserved or mildly reduced ejection fractions
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Transthyretin amyloidosis prevalence and characteristics in Korean patients with heart failure with preserved or mildly reduced ejection fractions ; volume:14 ; number:1 ; day:1 ; month:10 ; year:2024 ; pages:1-9 ; date:12.2024
Scientific reports ; 14, Heft 1 (1.10.2024), 1-9, 12.2024
- Creator
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Kim, Se-Eun
Lee, Sang-Hyup
Oh, Jaewon
Lee, Chan Joo
Hwang, Sang Hyun
Kang, Won Jun
Kang, Seok-Min
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-024-74191-0
- URN
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urn:nbn:de:101:1-2412182123208.259987186817
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:21 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kim, Se-Eun
- Lee, Sang-Hyup
- Oh, Jaewon
- Lee, Chan Joo
- Hwang, Sang Hyun
- Kang, Won Jun
- Kang, Seok-Min
- SpringerLink (Online service)
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Multidisciplinary Approaches for Transthyretin Amyloidosis
Analysis of disease progression in patients with transthyretin cardiac amyloidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
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Hereditary transthyretin amyloidosis overview
Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Multidisciplinary Approaches for Transthyretin Amyloidosis
Analysis of disease progression in patients with transthyretin cardiac amyloidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
Sex differences in transthyretin cardiac amyloidosis
Hereditary transthyretin amyloidosis: a case report
Sex Differences in Wild-Type Transthyretin Amyloidosis: An Analysis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
Effects of Tafamidis on Transthyretin Stabilization and Clinical Outcomes in Patients with Non-Val30Met Transthyretin Amyloidosis
Hereditary transthyretin amyloidosis overview
Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Multidisciplinary Approaches for Transthyretin Amyloidosis
Analysis of disease progression in patients with transthyretin cardiac amyloidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
Sex differences in transthyretin cardiac amyloidosis
Hereditary transthyretin amyloidosis: a case report
Sex Differences in Wild-Type Transthyretin Amyloidosis: An Analysis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)