- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1532-429X
- Umfang
-
Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Myocardial iron overload in thalassemia major. How early to check? ; volume:16 ; number:1 ; day:16 ; month:1 ; year:2014 ; pages:1-3 ; date:1.2014
Journal of cardiovascular magnetic resonance ; 16, Heft 1 (16.1.2014), 1-3, 1.2014
- Urheber
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Meloni, Antonella
- Beteiligte Personen und Organisationen
-
Borgna-Pignatti, Caterina
Guerrini, Giulia
Positano, Vincenzo
Filosa, Aldo
Ruffo, Giovan Battista
Casini, Tommaso
Chiodi, Elisabetta
Lombardi, Massimo
Pepe, Alessia
SpringerLink (Online service)
- DOI
-
10.1186/1532-429X-16-S1-P254
- URN
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urn:nbn:de:1111-2016032316703
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:01 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- Meloni, Antonella
- Borgna-Pignatti, Caterina
- Guerrini, Giulia
- Positano, Vincenzo
- Filosa, Aldo
- Ruffo, Giovan Battista
- Casini, Tommaso
- Chiodi, Elisabetta
- Lombardi, Massimo
- Pepe, Alessia
- SpringerLink (Online service)
Ähnliche Objekte (12)
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MRI assessment of correlation between cardiac biventricular function, myocardial iron overload and pancreatic iron overload in a large cohort of thalassemia major patients
Right ventricular volumes and function in thalassemia major patients in the absence of myocardial iron overload
Effect of deferiprone or deferoxamine on right ventricular function in thalassemia major patients with myocardial iron overload
Erythrocyte labile iron pool indicating concealed iron overload in non-transfusion-dependent β-thalassemia
Ventricular function and volume assessment in children, adolescents and young adults with thalassemia major without myocardial iron overload
Global longitudinal strain as an Indicator of cardiac Iron overload in thalassemia patients
Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy
Different patterns of myocardial iron overload by T2* Cardiovascular MR as markers of risk for cardiac complication in thalassemia major
Pulmonary function in patients with transfusion-dependent thalassemia and its associations with iron overload
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Cardiac MR images of thalassemia major patients with myocardial iron overload: a data note
An automatic method for myocardial T2* curve fitting in thalassemia patients with severe iron overload
MRI assessment of correlation between cardiac biventricular function, myocardial iron overload and pancreatic iron overload in a large cohort of thalassemia major patients
Right ventricular volumes and function in thalassemia major patients in the absence of myocardial iron overload
Effect of deferiprone or deferoxamine on right ventricular function in thalassemia major patients with myocardial iron overload
Erythrocyte labile iron pool indicating concealed iron overload in non-transfusion-dependent β-thalassemia
Ventricular function and volume assessment in children, adolescents and young adults with thalassemia major without myocardial iron overload
Global longitudinal strain as an Indicator of cardiac Iron overload in thalassemia patients
Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy
Different patterns of myocardial iron overload by T2* Cardiovascular MR as markers of risk for cardiac complication in thalassemia major
Pulmonary function in patients with transfusion-dependent thalassemia and its associations with iron overload
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Cardiac MR images of thalassemia major patients with myocardial iron overload: a data note
An automatic method for myocardial T2* curve fitting in thalassemia patients with severe iron overload
MRI assessment of correlation between cardiac biventricular function, myocardial iron overload and pancreatic iron overload in a large cohort of thalassemia major patients
Right ventricular volumes and function in thalassemia major patients in the absence of myocardial iron overload
Effect of deferiprone or deferoxamine on right ventricular function in thalassemia major patients with myocardial iron overload
Erythrocyte labile iron pool indicating concealed iron overload in non-transfusion-dependent β-thalassemia
Ventricular function and volume assessment in children, adolescents and young adults with thalassemia major without myocardial iron overload
Global longitudinal strain as an Indicator of cardiac Iron overload in thalassemia patients
Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy
Different patterns of myocardial iron overload by T2* Cardiovascular MR as markers of risk for cardiac complication in thalassemia major