Fabry disease (FD) is a rare lysosomal storage disorder also affecting the heart. The aims of this study were to determine the frequency of cardiac troponin I (cTNI) elevation, a sensitive parameter reflecting myocardial damage, in a smaller cohort of FD-patients, and to analyze whether persistent cTNI can be a suitable biomarker to assess cardiac dysfunction in FD.cTNI values were determined at least twice per year in 14 FD-patients (6 males and 8 females) regularly followed-up in our centre. The data were related to other parameters of heart function including cardiac magnetic resonance imaging (cMRI).Three patients (21%) without specific vascular risk factors other than FD had persistent cTNI-elevations (range 0.05-0.71 ng/ml, normal: <0...
Objective Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac i...
Current therapies have not shown benefit in organ damage reversal in Fabry disease (FD), but biomark...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
Objectives: Assessment of the clinical severity of Fabry disease (FD), an X-linked, rare, progressiv...
Background Cardiovascular magnetic resonance can demonstrate myocardial processes in Fabry disease (...
Abstract Although Fabry disease was identified a century ago, it is still a challenging condition to...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
Background High‐sensitivity troponin (hs‐TNT), a biomarker of myocardial damage, might be useful fo...
Background-Chest pain is frequently reported in Fabry disease (FD). However, its mechanism and clini...
Fabry disease (FD) is an X-linked genetic disorder of glycosphingolipid metabolism due to deficiency...
BACKGROUND Cardiac response to enzyme replacement therapy (ERT) in Fabry disease is typically ass...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
<p>Presented are patients with Fabry disease (FD) and left ventricular hypertrophy (LVH) (n = 17) ve...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the galactosidas...
Objective Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac i...
Current therapies have not shown benefit in organ damage reversal in Fabry disease (FD), but biomark...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...
Objectives: Assessment of the clinical severity of Fabry disease (FD), an X-linked, rare, progressiv...
Background Cardiovascular magnetic resonance can demonstrate myocardial processes in Fabry disease (...
Abstract Although Fabry disease was identified a century ago, it is still a challenging condition to...
BACKGROUND: Cardiovascular magnetic resonance (CMR) derived native myocardial T1 is decreased in pat...
[[abstract]]Fabry disease (FD) is an X-linked, rare inherited lysosomal storage disease caused by al...
Background High‐sensitivity troponin (hs‐TNT), a biomarker of myocardial damage, might be useful fo...
Background-Chest pain is frequently reported in Fabry disease (FD). However, its mechanism and clini...
Fabry disease (FD) is an X-linked genetic disorder of glycosphingolipid metabolism due to deficiency...
BACKGROUND Cardiac response to enzyme replacement therapy (ERT) in Fabry disease is typically ass...
Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galact...
<p>Presented are patients with Fabry disease (FD) and left ventricular hypertrophy (LVH) (n = 17) ve...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the galactosidas...
Objective Cardiac magnetic resonance (CMR) has the potential to provide early detection of cardiac i...
Current therapies have not shown benefit in organ damage reversal in Fabry disease (FD), but biomark...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder manifesting as progressive multi-or...