- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Guideline of transthyretin-related hereditary amyloidosis for clinicians ; volume:8 ; number:1 ; day:20 ; month:2 ; year:2013 ; pages:1-18 ; date:12.2013
Orphanet journal of rare diseases ; 8, Heft 1 (20.2.2013), 1-18, 12.2013
- Creator
-
Ando, Yukio
- Contributor
-
Coelho, Teresa
Berk, John L.
Cruz, Márcia Waddington
Ericzon, Bo-Göran
Ikeda, Shu-Ichi
Lewis, W David
Obici, Laura
Planté-Bordeneuve, Violaine
Rapezzi, Claudio
Said, Gerard
Salvi, Fabrizio
SpringerLink (Online service)
- DOI
-
10.1186/1750-1172-8-31
- URN
-
urn:nbn:de:1111-2016050122824
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:50 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
- Ando, Yukio
- Coelho, Teresa
- Berk, John L.
- Cruz, Márcia Waddington
- Ericzon, Bo-Göran
- Ikeda, Shu-Ichi
- Lewis, W David
- Obici, Laura
- Planté-Bordeneuve, Violaine
- Rapezzi, Claudio
- Said, Gerard
- Salvi, Fabrizio
- SpringerLink (Online service)
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Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Symptoms of Hereditary Transthyretin Amyloidosis: The Patient and Physician Perspective
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study
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Hereditary transthyretin amyloidosis: a case report
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Conjunctival lymphangiectasia and retinal angiopathy in hereditary transthyretin amyloidosis
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Symptoms of Hereditary Transthyretin Amyloidosis: The Patient and Physician Perspective
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study