Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcomes data from the Fabry Outcome Survey (FOS), 10-year data were analyzed. Patients and methods: FOS (ClinicalTrials.gov identifier: NCT03289065) data (April 2001 to August 2018) were retrospectively analyzed. Estimated glomerular filtration rate (eGFR) and left ventricular mass indexed to height (LVMI) were analyzed after treatment start (baseline) for patients with ≥3 measurements, including baseline and year 10. Results: Median (range) age (years) of the evaluable treated renal cohort at treatment start was 48.8 (17.9-67.3) for females (n=62), 34.4 (18.0-66.8) for males (n=90). With eGFR ≥60 mL/min/1.73 m at baseline, mean (95% CI) rate of e...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Outcomes from 5 years of treatment with agalsidase alfa enzyme replacement therapy (ERT) for Fabry d...
Agalsidasa alfa; Teràpia de reemplaçament enzimàtic; Malaltia de FabryAgalsidasa alfa; Terapia de re...
Background: We analysed 5-year treatment with agalsidase alfa enzyme replacement therapy in patients...
Aims: Long-term treatment effect studies in large female Fabry patient groups are challenging to des...
Altres ajuts: This work was supported by Shire International GmbH.This is a retrospective analysis o...
Derralynn Hughes,1 Aleš Linhart,2 Andrey Gurevich,3 Vasiliki Kalampoki,3 Dalia Jazukeviciene,3 Sandr...
<div><p>Despite enzyme replacement therapy, disease progression is observed in patients with Fabry d...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Background. In Fabry disease, end-stage renal disease (ESRD) and severe neurologic and cardiac compl...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Outcomes from 5 years of treatment with agalsidase alfa enzyme replacement therapy (ERT) for Fabry d...
Agalsidasa alfa; Teràpia de reemplaçament enzimàtic; Malaltia de FabryAgalsidasa alfa; Terapia de re...
Background: We analysed 5-year treatment with agalsidase alfa enzyme replacement therapy in patients...
Aims: Long-term treatment effect studies in large female Fabry patient groups are challenging to des...
Altres ajuts: This work was supported by Shire International GmbH.This is a retrospective analysis o...
Derralynn Hughes,1 Aleš Linhart,2 Andrey Gurevich,3 Vasiliki Kalampoki,3 Dalia Jazukeviciene,3 Sandr...
<div><p>Despite enzyme replacement therapy, disease progression is observed in patients with Fabry d...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Background. In Fabry disease, end-stage renal disease (ESRD) and severe neurologic and cardiac compl...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...