Analysis of disease progression in patients with transthyretin cardiac amyloidosis
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Analysis of disease progression in patients with transthyretin cardiac amyloidosis ; volume:10 ; number:1 ; day:2 ; month:11 ; year:2015 ; pages:1 ; date:12.2015
Orphanet journal of rare diseases ; 10, Heft 1 (2.11.2015), 1, 12.2015
- Creator
-
Gilmore, Julian D.
Maurer, Mathew S.
Vest, John
Karsten, Verena
Powell, Christine
Strahs, Andrew
Gollob, Jared
Hawkins, Philip N.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/1750-1172-10-S1-O10
- URN
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urn:nbn:de:101:1-2020100521482085401127
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:59 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
- Gilmore, Julian D.
- Maurer, Mathew S.
- Vest, John
- Karsten, Verena
- Powell, Christine
- Strahs, Andrew
- Gollob, Jared
- Hawkins, Philip N.
- SpringerLink (Online service)
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Negative bone scintigraphy in wild-type transthyretin cardiac amyloidosis
Amyloid seeding as a disease mechanism and treatment target in transthyretin cardiac amyloidosis
Multimodality imaging of simultaneous occurrence of cardiac transthyretin amyloidosis and cardiac sarcoidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
Imaging modalities in early cardiac transthyretin amyloidosis: who is first?
Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression
Multidisciplinary Approaches for Transthyretin Amyloidosis
Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report
Pre-symptomatic scintigraphic and genetic cascade screening in cardiac transthyretin amyloidosis
Hereditary transthyretin amyloidosis: a case report
Sex differences in transthyretin cardiac amyloidosis
Hereditary transthyretin amyloidosis overview
Negative bone scintigraphy in wild-type transthyretin cardiac amyloidosis
Amyloid seeding as a disease mechanism and treatment target in transthyretin cardiac amyloidosis
Multimodality imaging of simultaneous occurrence of cardiac transthyretin amyloidosis and cardiac sarcoidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
Imaging modalities in early cardiac transthyretin amyloidosis: who is first?
Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression
Multidisciplinary Approaches for Transthyretin Amyloidosis
Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report
Pre-symptomatic scintigraphic and genetic cascade screening in cardiac transthyretin amyloidosis