In spite of several research studies help to describe the heart in Fabry disease (FD), the cardiomyopathy is not entirely understood. In addition, the impact of blood pressure and alterations in geometry have not been systematically evaluated.In 74 FD patients (mean age 36±12 years; 45 females) the extent of myocardial fibrosis and its progression were quantified using cardiac magnetic-resonance-imaging with late enhancement technique (LE). Results were compared to standard echocardiography complemented by 2D-speckle-tracking, 3D-sphericity-index (SI) and standardized blood pressure measurement. At baseline, no patient received enzyme replacement therapy (ERT). After 51±24 months, a follow-up examination was performed.Systolic blood pressur...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
AIMS Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular hypertrophy (LVH)...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
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...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), th...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
ObjectivesWe hypothesized that Fabry cardiomyopathy in female patients might differ substantially fr...
BACKGROUND: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid stor...
In Anderson-Fabry disease (AFD) the impact of left ventricular (LV) function on cardiac outcome is u...
AIMS: Fabry cardiomyopathy is characterized by glycosphingolipid storage and increased myocardial tr...
Echocardiography plays a key role in the evaluation of functional and structural changes of the hear...
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 (...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
AIMS Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular hypertrophy (LVH)...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
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...
Background In spite of several research studies help to describe the heart in Fabry disease (FD), th...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
ObjectivesWe hypothesized that Fabry cardiomyopathy in female patients might differ substantially fr...
BACKGROUND: In prehypertrophic Fabry disease, low myocardial T1 values, reflecting sphingolipid stor...
In Anderson-Fabry disease (AFD) the impact of left ventricular (LV) function on cardiac outcome is u...
AIMS: Fabry cardiomyopathy is characterized by glycosphingolipid storage and increased myocardial tr...
Echocardiography plays a key role in the evaluation of functional and structural changes of the hear...
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 (...
International audiencePURPOSE:To evaluate the potential of non-contrast myocardial T1 mapping on car...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
AIMS Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular hypertrophy (LVH)...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...