Background and objectives: These analyses were designed to characterize renal disease progression in untreated adults with Fabry disease. Design, setting, participants, & measurements: Data from the Fabry Registry for 462 untreated adults (121 men and 341 women) who had at least two estimated GFR (eGFR) values over a span of ≥12 months before starting enzyme replacement therapy were included. Results: Most men (86 of 121, 71%) had more rapid loss of kidney function than the normal adult population (loss of eGFR > −1 ml/min per 1.73 m2 per year), whereas fewer women (133 of 341, 39%) had rapid loss of kidney function. Patients with rapid progression had significantly higher mean averaged urinary protein to urinary creatinine ratios (UP/C...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Background. In Fabry disease, progressive glycolipid ac-cumulation leads to organ damage and early d...
Background and objectives: These analyses were designed to characterize renal disease progression in...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
BACKGROUND: Fabry disease, an X-linked genetic disorder with deficient alpha-galactosidase A activit...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BackgroundIn Fabry disease, progressive glycolipid accumulation leads to organ damage and early demi...
<div><p>Despite enzyme replacement therapy, disease progression is observed in patients with Fabry d...
Background. Renal and cardiac involvement is responsible for substantial morbidity and mortality in ...
BACKGROUND: In Fabry nephropathy, alpha-galactosidase deficiency leads to accumulation of glycosphin...
In Fabry disease, progressive glycolipid accumulation leads to organ damage and early demise, but th...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Background. In Fabry disease, progressive glycolipid ac-cumulation leads to organ damage and early d...
Background and objectives: These analyses were designed to characterize renal disease progression in...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
BACKGROUND: Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-gala...
BACKGROUND: Fabry disease, an X-linked genetic disorder with deficient alpha-galactosidase A activit...
Background/Aims: Fabry disease (FD) is a rare inherited lysosomal storage disease with common and se...
Background. The purpose of this study was to identify determinants of renal disease progression in a...
Despite enzyme replacement therapy, disease progression is observed in patients with Fabry disease. ...
BackgroundIn Fabry disease, progressive glycolipid accumulation leads to organ damage and early demi...
<div><p>Despite enzyme replacement therapy, disease progression is observed in patients with Fabry d...
Background. Renal and cardiac involvement is responsible for substantial morbidity and mortality in ...
BACKGROUND: In Fabry nephropathy, alpha-galactosidase deficiency leads to accumulation of glycosphin...
In Fabry disease, progressive glycolipid accumulation leads to organ damage and early demise, but th...
Aim: Fabry disease is a rare lysosomal storage disorder caused by deficient activity of alpha-galact...
To determine the impact of initiating enzyme replacement therapy (ERT) with agalsidase alfa early in...
Background. In Fabry disease, progressive glycolipid ac-cumulation leads to organ damage and early d...