Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
<p>Correlation analyses: (1) Plasma globotriaosylsphingosine (Lyso-Gb3) and plasma α-Gal A activity ...
Fabry disease is a rare lysosomal storage disorder caused by a deficiency of α-galactosidase A, resu...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
<p>P: Pain in peripheral extremities, A: Angiokeratomas, HH: Hypohidrosis, CO: Corneal opacities, RD...
Lyso-globotriaosylsphingosine (lyso-Gb(3)) is a useful biomarker in the diagnosis and monitoring of ...
AbstractFabry disease is an X-linked lysosomal storage disorder due to deficiency of alpha-Galactosi...
<p>The horizontal mark indicated the median. It is noteworthy that lyso-Gb3 levels in males are ∼10 ...
Der Morbus Fabry ist eine sehr heterogenetische und heterophänotypische Krankheit. Ursache der Erkra...
Biomarkers useful for diagnosis and evaluation of treatment for patients with Fabry disease are urge...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
For the first time in Lenkoran-Astara administrative area of Azerbaijan Republic, patients with card...
AbstractBackgroundPrevious studies revealed a high incidence of late-onset Fabry disease mutation, I...
Background: Fabry disease is characterized by accumulation of glycosphingolipids, such as globotriao...
Fabry's disease is a genetic disorder of X-linked inheritance caused by mutations in the alpha galac...
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
<p>Correlation analyses: (1) Plasma globotriaosylsphingosine (Lyso-Gb3) and plasma α-Gal A activity ...
Fabry disease is a rare lysosomal storage disorder caused by a deficiency of α-galactosidase A, resu...
BACKGROUND: Fabry disease (FD) is a rare X-linked lysosomal storage disorder due to mutations in the...
<p>P: Pain in peripheral extremities, A: Angiokeratomas, HH: Hypohidrosis, CO: Corneal opacities, RD...
Lyso-globotriaosylsphingosine (lyso-Gb(3)) is a useful biomarker in the diagnosis and monitoring of ...
AbstractFabry disease is an X-linked lysosomal storage disorder due to deficiency of alpha-Galactosi...
<p>The horizontal mark indicated the median. It is noteworthy that lyso-Gb3 levels in males are ∼10 ...
Der Morbus Fabry ist eine sehr heterogenetische und heterophänotypische Krankheit. Ursache der Erkra...
Biomarkers useful for diagnosis and evaluation of treatment for patients with Fabry disease are urge...
Fabry disease is an X-linked genetic disorder characterized by deficient activity of α-galactosidase...
For the first time in Lenkoran-Astara administrative area of Azerbaijan Republic, patients with card...
AbstractBackgroundPrevious studies revealed a high incidence of late-onset Fabry disease mutation, I...
Background: Fabry disease is characterized by accumulation of glycosphingolipids, such as globotriao...
Fabry's disease is a genetic disorder of X-linked inheritance caused by mutations in the alpha galac...
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
<p>Correlation analyses: (1) Plasma globotriaosylsphingosine (Lyso-Gb3) and plasma α-Gal A activity ...
Fabry disease is a rare lysosomal storage disorder caused by a deficiency of α-galactosidase A, resu...