Derralynn Hughes,1 Aleš Linhart,2 Andrey Gurevich,3 Vasiliki Kalampoki,3 Dalia Jazukeviciene,3 Sandro Feriozzi4 On behalf of the FOS Study Group1University College London and Royal Free London NHS Foundation Trust, London, UK; 2Charles University, First Faculty of Medicine, Prague, Czech Republic; 3Takeda Pharmaceuticals International AG, Zurich, Switzerland; 4Nephrology and Dialysis Unit, Belcolle Hospital, Department of Nephrology and Dialysis, Viterbo, ItalyCorrespondence: Derralynn HughesUniversity College London and Royal Free London NHS Foundation Trust, Pond Street, London, NW3 2QG, UKEmail derralynnhughes@nhs.netBackground: The timing of enzyme replacement therapy initiation in patients with Fabry disease is hypothesized to be criti...
Fabry disease is a rare lysosomal storage disorder caused by mutations in the GLA gene, which, witho...
Aims: Long-term treatment effect studies in large female Fabry patient groups are challenging to des...
Background. In Fabry disease, end-stage renal disease (ESRD) and severe neurologic and cardiac compl...
BACKGROUND: The timing of enzyme replacement therapy initiation in patients with Fabry disease is hy...
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...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Background: We analysed 5-year treatment with agalsidase alfa enzyme replacement therapy in patients...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
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...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
Background Agalsidase beta is a form of enzyme replacement therapy for Fabry disease, a genetic di...
Background: Enzyme replacement therapy (ERT) slows disease progression of Fabry disease (FD), especi...
Fabry disease is a rare lysosomal storage disorder caused by mutations in the GLA gene, which, witho...
Aims: Long-term treatment effect studies in large female Fabry patient groups are challenging to des...
Background. In Fabry disease, end-stage renal disease (ESRD) and severe neurologic and cardiac compl...
BACKGROUND: The timing of enzyme replacement therapy initiation in patients with Fabry disease is hy...
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...
PURPOSE: The initiation of enzyme-replacement therapy prior to the occurrence of substantial and irr...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Background: We analysed 5-year treatment with agalsidase alfa enzyme replacement therapy in patients...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
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...
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcom...
Background Agalsidase beta is a form of enzyme replacement therapy for Fabry disease, a genetic di...
Background: Enzyme replacement therapy (ERT) slows disease progression of Fabry disease (FD), especi...
Fabry disease is a rare lysosomal storage disorder caused by mutations in the GLA gene, which, witho...
Aims: Long-term treatment effect studies in large female Fabry patient groups are challenging to des...
Background. In Fabry disease, end-stage renal disease (ESRD) and severe neurologic and cardiac compl...