<p>P: Pain in peripheral extremities, A: Angiokeratomas, HH: Hypohidrosis, CO: Corneal opacities, RD: Renal disease, HD: Heart disease, and CV: Cerebrovascular disease. N: Not available. WT: Wild type</p><p>*Ref. 30.</p><p>Genotypes, plasma lyso-Gb3 concentrations, and clinical manifestations in the patients with Fabry disease.</p
Fabry disease is a multisystemic lysosomal storage disorder caused by the impairment of α-galactosid...
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
Fabry disease is an X linked illness caused by mutation in the GLA gene which codes lysosomal enzyme...
Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Background: Screening for Fabry disease (FD) in high risk populations yields a significant number of...
Numerous α-galactosidase A (α-gal A) gene (GLA) mutations have been identified in Fabry disease (FD)...
<div><p>Numerous α-galactosidase A (α-gal A) gene (GLA) mutations have been identified in Fabry dise...
Fabry disease is an X-linked genetic deficiency in the alpha-galactosidase enzyme resulting in intra...
Fabry disease' (FD) phenotype is heterogeneous: alpha-galactosidase A gene mutations (GLA) can lead ...
<p>Correlation analyses: (1) Plasma globotriaosylsphingosine (Lyso-Gb3) and plasma α-Gal A activity ...
Fabry disease (FD) (Anderson-Fabry disease, OMIM 301500) is a genetic disorder caused by a pathogeni...
Patient: Male, 39 Final Diagnosis: Fabry disease Symptoms: - Acropareshesia . fatique Medic...
Background Anderson–Fabry disease (FD) is an X-linked lysosomal storage disorder with varying organ...
Background: Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by 	...
Fabry disease is a multisystemic lysosomal storage disorder caused by the impairment of α-galactosid...
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
Fabry disease is an X linked illness caused by mutation in the GLA gene which codes lysosomal enzyme...
Genetic characterization and plasma levels of Lyso Gb3 assessed in Fabry disease patients.</p
Fabry disease is a lysosomal storage disorder with an X-linked pattern of inheritance. Fabry disease...
Background: Screening for Fabry disease (FD) in high risk populations yields a significant number of...
Numerous α-galactosidase A (α-gal A) gene (GLA) mutations have been identified in Fabry disease (FD)...
<div><p>Numerous α-galactosidase A (α-gal A) gene (GLA) mutations have been identified in Fabry dise...
Fabry disease is an X-linked genetic deficiency in the alpha-galactosidase enzyme resulting in intra...
Fabry disease' (FD) phenotype is heterogeneous: alpha-galactosidase A gene mutations (GLA) can lead ...
<p>Correlation analyses: (1) Plasma globotriaosylsphingosine (Lyso-Gb3) and plasma α-Gal A activity ...
Fabry disease (FD) (Anderson-Fabry disease, OMIM 301500) is a genetic disorder caused by a pathogeni...
Patient: Male, 39 Final Diagnosis: Fabry disease Symptoms: - Acropareshesia . fatique Medic...
Background Anderson–Fabry disease (FD) is an X-linked lysosomal storage disorder with varying organ...
Background: Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by 	...
Fabry disease is a multisystemic lysosomal storage disorder caused by the impairment of α-galactosid...
Fabry disease (FD), a lysosomal storage disorder caused by α-galactosidase A (GLA) gene variants, ha...
Fabry disease is an X linked illness caused by mutation in the GLA gene which codes lysosomal enzyme...