In the past few years, the wide application of cardiac magnetic resonance (CMR) significantly changed the approach to the study of cardiac involvement in Fabry Disease (FD). The possibility to perform non-invasive tissue characterization, including new sequences such as T1/T2 mapping, offered a powerful tool for differential diagnosis with other forms of left ventricular hypertrophy. In patients with confirmed diagnosis of FD, CMR is the most sensitive non-invasive technique for early detection of cardiac involvement and it provides new insight into the evolution of cardiac damage, including gender-specific features. Finally, CMR multiparametric detection of subtle changes in cardiac morphology, function and tissue composition is potentiall...
Abstract The Anderson-Fabry disease (AFD, or simply Fabry Disease, FD; MIM #301500) is a rare X-link...
The variation of morphological and functional cardiac manifestation in Fabry disease: potential impl...
Abstract Background Although it is known that Anderso...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
Objective Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac i...
Fabry disease (FD) is a genetic lysosomal storage disease with frequent cardiovascular involvement, ...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
BackgroundCardiovascular disease is the most common cause of death among Fabry disease patients, who...
Anderson-Fabry (FD) disease is a rare X-linked disorder caused by different mutations in the Galacto...
Fabry's disease is a multisystem X-linked disorder of lysosomal metabolism frequently associated wit...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
Abstract Although Fabry disease was identified a century ago, it is still a challenging condition to...
Background Cardiovascular magnetic resonance can demonstrate myocardial processes in Fabry disease (...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
Abstract The Anderson-Fabry disease (AFD, or simply Fabry Disease, FD; MIM #301500) is a rare X-link...
The variation of morphological and functional cardiac manifestation in Fabry disease: potential impl...
Abstract Background Although it is known that Anderso...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
Objective Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac i...
Fabry disease (FD) is a genetic lysosomal storage disease with frequent cardiovascular involvement, ...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
BackgroundCardiovascular disease is the most common cause of death among Fabry disease patients, who...
Anderson-Fabry (FD) disease is a rare X-linked disorder caused by different mutations in the Galacto...
Fabry's disease is a multisystem X-linked disorder of lysosomal metabolism frequently associated wit...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
Abstract Although Fabry disease was identified a century ago, it is still a challenging condition to...
Background Cardiovascular magnetic resonance can demonstrate myocardial processes in Fabry disease (...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
Abstract The Anderson-Fabry disease (AFD, or simply Fabry Disease, FD; MIM #301500) is a rare X-link...
The variation of morphological and functional cardiac manifestation in Fabry disease: potential impl...
Abstract Background Although it is known that Anderso...