Background: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid storage, are associated with early structural and ECG changes. The correlations between T1 values and functional parameters have not been explored. Furthermore, the potential prognostic role of T1 in predicting disease worsening is still unknown. Methods: ECG, 2D echocardiography, cardiopulmonary test, and cardiac magnetic resonance were performed in 44 Fabry patients without left ventricular hypertrophy (35.7±14.5 years, 68.2% females). After a 12-month follow-up, clinical stability was evaluated using Fabry Stabilization Index. Results: At baseline, T1 values showed a negative correlation with left ventricular mass ( r=-0.79; P<0.0001)...
In Anderson-Fabry disease (AFD) the impact of left ventricular (LV) function on cardiac outcome is u...
Background: Various electrocardiographic (ECG) indices have been shown to be useful for early recogn...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
BACKGROUND: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid stor...
AIMS Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular hypertrophy (LVH)...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), ...
BACKGROUND/nIn spite of several research studies help to describe the heart in Fabry disease (FD), t...
BackgroundThe cardiac manifestations of Fabry disease are the leading cause of death, but risk strat...
In spite of several research studies help to describe the heart in Fabry disease (FD), the cardiomyo...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), th...
BACKGROUND Cardiac response to enzyme replacement therapy (ERT) in Fabry disease is typically ass...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
In this retrospective, observational study, 45 patients with Anderson-Fabry disease (AFD) underwent ...
International audienceBackground: Screening for Fabry disease is sub-optimal in non-specialised cent...
In Anderson-Fabry disease (AFD) the impact of left ventricular (LV) function on cardiac outcome is u...
Background: Various electrocardiographic (ECG) indices have been shown to be useful for early recogn...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
BACKGROUND: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid stor...
AIMS Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular hypertrophy (LVH)...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), ...
BACKGROUND/nIn spite of several research studies help to describe the heart in Fabry disease (FD), t...
BackgroundThe cardiac manifestations of Fabry disease are the leading cause of death, but risk strat...
In spite of several research studies help to describe the heart in Fabry disease (FD), the cardiomyo...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), th...
BACKGROUND Cardiac response to enzyme replacement therapy (ERT) in Fabry disease is typically ass...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
In this retrospective, observational study, 45 patients with Anderson-Fabry disease (AFD) underwent ...
International audienceBackground: Screening for Fabry disease is sub-optimal in non-specialised cent...
In Anderson-Fabry disease (AFD) the impact of left ventricular (LV) function on cardiac outcome is u...
Background: Various electrocardiographic (ECG) indices have been shown to be useful for early recogn...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...