Mie scattering is increasingly exploited to manipulate electromagnetic fields to achieve
strong resonant enhancement, to obtain perfect absorption of radiation, and to generate …

Anderson-Fabry disease is an X-linked inborn error of glycosphingolipid catabolism caused
by a deficiency of α-galactosidase A. The incidence ranges between 1: 40,000 and 1 …

Fabry disease leads to renal, cardiac, and cerebrovascular manifestations. Phenotypic
differences between classically and nonclassically affected patients are evident, but there …

Abstract Background Lysosomal storage diseases (LSDs) are inborn errors of metabolism
resulting from 50 different inherited disorders. The increasing availability of treatments and …

Purpose of review: In this narrative review, we describe general aspects, histological
alterations, treatment, and implications of Fabry disease (FD) nephropathy. This information …

Anderson-Fabry disease (AFD) is an X-linked lysosomal storage disorder caused by
deficient activity of the enzyme alpha-galactosidase. While AFD is recognized as a …

Fabry disease is a rare X-linked lysosomal storage disorder due to mutations in the GLA
gene causing complete or partial deficiency of the enzyme a-galactosidase A (a-Gal A), and …

Fabry disease is a lysosomal storage disease caused by mutations in the GLA gene that
encodes alpha-galactosidase (AGAL). The disease causes abnormal globotriaosylceramide …

Fabry disease (FD) is a rare inherited disorder characterized by a wide range of systemic
symptoms; it is particularly associated with cardiovascular and renal problems. Enzyme …

Fabry disease (FD) is an X-linked inherited lysosomal disorder due to a deficiency of the
enzyme alpha-galactosidase A (α-gla) due to mutations in the GLA gene. These mutations …