Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis
- 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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Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis ; volume:19 ; number:1 ; day:5 ; month:12 ; year:2024 ; pages:1-10 ; date:12.2024
Orphanet journal of rare diseases ; 19, Heft 1 (5.12.2024), 1-10, 12.2024
- Creator
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Canciello, Grazia
Tozza, Stefano
Todde, Gaetano
Nolano, Maria
Borrelli, Felice
Palumbo, Giovanni
Lombardi, Raffaella
Cassano, Emanuele
Acampa, Wanda
Esposito, Giovanni
Manganelli, Fiore
Losi, Maria Angela
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-024-03473-7
- URN
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urn:nbn:de:101:1-2502192118093.024794564555
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 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
- Canciello, Grazia
- Tozza, Stefano
- Todde, Gaetano
- Nolano, Maria
- Borrelli, Felice
- Palumbo, Giovanni
- Lombardi, Raffaella
- Cassano, Emanuele
- Acampa, Wanda
- Esposito, Giovanni
- Manganelli, Fiore
- Losi, Maria Angela
- SpringerLink (Online service)
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Multidisciplinary Approaches for Transthyretin Amyloidosis
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Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression
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Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus
Hereditary transthyretin amyloidosis overview
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
Multidisciplinary Approaches for Transthyretin Amyloidosis
Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report
Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression
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)
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