<p><b>A.</b> The GLA concentrations in the serum samples from male patients with classic Fabry disease (Male Fabry), male subjects with p.E66Q (E66Q), and control subjects (Control). <b>B.</b> The GLA concentrations in the plasma samples collected from male patients with classic Fabry disease (Male Fabry), female patients with Fabry disease (Female Fabry), male subjects with p.E66Q (E66Q), and controls (Control). Statistically significant differences are marked with asterisks: *p<0.05; **p<0.01; ***p<0.001. All experimental data are shown as the mean (bold horizontal bars) ± S.D. (Error bars). <b>C.</b> The relationship between the enzymatic activity and protein level of GLA in the serum. <b>D.</b> The relationship between the enzymatic act...
Fabry disease is caused by mutations in the GLA gene that lower α-galactosidase A activity to less t...
<p>The horizontal mark indicated the median. It is noteworthy that lyso-Gb3 levels in males are ∼10 ...
Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p
<p><b>A.</b> The GLA concentrations in the serum samples collected from male patients with classic F...
<div><p>Fabry disease is an X-linked genetic disorder caused by defects in the α-galactosidase A (<i...
Fabry disease is an X-linked genetic disorder caused by defects in the a-galactosidase A (GLA) gene,...
Fabry disease is an X-linked genetic disorder caused by defects in the α-galactosidase A (GLA) gene,...
<p>A. The relationship between the anti- Aga-A antibody level and anti-Aga-B antibody one measured b...
<p><sup>1)</sup>Aga-A; agalsidase alpha</p><p><sup>2)</sup>Aga-B; agalsidase beta</p><p><sup>3)</sup...
<p>Sera from 29 Fabry patients (#1–29) and controls (Cont) were assayed by ELISA (left side) and IC ...
<p>Standard curve of the GLA protein concentration in serum (<b>A</b>) and plasma (<b>B</b>). In eac...
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of alpha-galac...
Fabry disease is caused by mutations in the GLA gene that lower α-galactosidase A activity to less t...
<p>The horizontal mark indicated the median. It is noteworthy that lyso-Gb3 levels in males are ∼10 ...
Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p
<p><b>A.</b> The GLA concentrations in the serum samples collected from male patients with classic F...
<div><p>Fabry disease is an X-linked genetic disorder caused by defects in the α-galactosidase A (<i...
Fabry disease is an X-linked genetic disorder caused by defects in the a-galactosidase A (GLA) gene,...
Fabry disease is an X-linked genetic disorder caused by defects in the α-galactosidase A (GLA) gene,...
<p>A. The relationship between the anti- Aga-A antibody level and anti-Aga-B antibody one measured b...
<p><sup>1)</sup>Aga-A; agalsidase alpha</p><p><sup>2)</sup>Aga-B; agalsidase beta</p><p><sup>3)</sup...
<p>Sera from 29 Fabry patients (#1–29) and controls (Cont) were assayed by ELISA (left side) and IC ...
<p>Standard curve of the GLA protein concentration in serum (<b>A</b>) and plasma (<b>B</b>). In eac...
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of alpha-galac...
Fabry disease is caused by mutations in the GLA gene that lower α-galactosidase A activity to less t...
<p>The horizontal mark indicated the median. It is noteworthy that lyso-Gb3 levels in males are ∼10 ...
Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p