Fabry disease may be treated by enzyme replacement therapy (ERT), but the impact of chronic kidney disease (CKD) on the response to therapy remains unclear. The aim of the present study was to analyse the incidence and predictors of clinical events in patients on ERT. Study design: Multicentre retrospective observational analysis of patients diagnosed and treated with ERT for Fabry disease. The primary outcome was the first renal, neurological or cardiological events or death during a follow-up of 60 months (24-120). Results: In 69 patients (42 males, 27 females, mean age 44.6±13.7 years), at the end of follow-up, eGFR and the left ventricular septum thickness remained stable and the urinary albumin: creatinine ratio tended to decrease, but...
Background Enzyme replacement therapy (ERT) slows disease progression of Fabry disease (FD), especi...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Enzyme replacement therapy (ERT) with recombinant human α-galactosidase A (r-hαGalA) enhances microv...
Fabry disease (FD) is an X-linked lysosomal storage disease caused by a deficiency in the enzyme, α-...
Background. Renal and cardiac involvement is responsible for substantial morbidity and mortality in ...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BACKGROUND/AIMS Fabry disease (FD) is a rare inherited lysosomal storage disease with common and ...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BACKGROUND: The timing of enzyme replacement therapy initiation in patients with Fabry disease is hy...
The long-term effects of enzyme-replacement therapy (ERT) in Fabry disease are unknown. Thus, the ai...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Aims: Fabry disease (FD) is a rare X-linked lysosomal storage disease with a deficiency of α-galactos...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
Background Enzyme replacement therapy (ERT) slows disease progression of Fabry disease (FD), especi...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Enzyme replacement therapy (ERT) with recombinant human α-galactosidase A (r-hαGalA) enhances microv...
Fabry disease (FD) is an X-linked lysosomal storage disease caused by a deficiency in the enzyme, α-...
Background. Renal and cardiac involvement is responsible for substantial morbidity and mortality in ...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BACKGROUND/AIMS Fabry disease (FD) is a rare inherited lysosomal storage disease with common and ...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BACKGROUND: The timing of enzyme replacement therapy initiation in patients with Fabry disease is hy...
The long-term effects of enzyme-replacement therapy (ERT) in Fabry disease are unknown. Thus, the ai...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Aims: Fabry disease (FD) is a rare X-linked lysosomal storage disease with a deficiency of α-galactos...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
Background Enzyme replacement therapy (ERT) slows disease progression of Fabry disease (FD), especi...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Enzyme replacement therapy (ERT) with recombinant human α-galactosidase A (r-hαGalA) enhances microv...