Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1619-1560
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis ; volume:29 ; number:1 ; day:26 ; month:8 ; year:2019 ; pages:45-53 ; date:9.2019
Clinical autonomic research ; 29, Heft 1 (26.8.2019), 45-53, 9.2019
- Urheber
-
Puig-Carrion, Gisela D.
Reyentovich, Alex
Katz, Stuart D.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s10286-019-00629-5
- URN
-
urn:nbn:de:101:1-2020020420591041704242
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Puig-Carrion, Gisela D.
- Reyentovich, Alex
- Katz, Stuart D.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Hereditary transthyretin amyloidosis overview
Hereditary transthyretin amyloidosis: a case report
Guideline of transthyretin-related hereditary amyloidosis for clinicians
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
Imaging cardiac innervation in hereditary transthyretin (ATTRm) amyloidosis: A marker for neuropathy or cardiomyopathy in case of heart failure?
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
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
Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
Hereditary transthyretin amyloidosis overview
Hereditary transthyretin amyloidosis: a case report
Guideline of transthyretin-related hereditary amyloidosis for clinicians
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
Imaging cardiac innervation in hereditary transthyretin (ATTRm) amyloidosis: A marker for neuropathy or cardiomyopathy in case of heart failure?
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
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
Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
Hereditary transthyretin amyloidosis overview
Hereditary transthyretin amyloidosis: a case report
Guideline of transthyretin-related hereditary amyloidosis for clinicians
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
Imaging cardiac innervation in hereditary transthyretin (ATTRm) amyloidosis: A marker for neuropathy or cardiomyopathy in case of heart failure?
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
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