Russian
болезнь фабри Portuguese
doença de fabry Spanish
enfermedad de fabry Catalan
malaltia d'anderson-fabry 
Rare human genetic lysosomal storage disorder.
1
The fd coat protein was purified by gel chromatography of the SDA solubilized virus.
2
These findings make fd bacteriophage a valuable tool for immunization without administering exogenous adjuvants.
3
In order to investigate the mechanisms of this activity, RNA-Sequencing of fd-pulsed dendritic cells was performed.
4
The minor coat proteins of the filamentous bacteriophage fl and fd have been isolated and characterized.
5
These findings may guide program planning for future FD to support IPE.
1
Recent advances in enzyme replacement therapy can reverse the storage of glycosphingolipids in Fabry's disease.
2
The diagnosis of Fabry's disease was made by the absence of plasma alpha-galactosidase A activity.
3
Thus, in patients with cardiac hypertrophy, it is important to differentiate Fabry's disease from other causes of hypertrophy.
4
This was a very rare case of subclinical Fabry's disease coexistent with cholesterol crystal embolization, mimicking pulmonary-renal syndrome.
1
Tinnitus may be an earlier symptom than previously thought in Fabry disease.
2
This paper examines hearing loss in a group of young patients with Fabry disease.
3
Objective: To assess the prevalence of Fabry disease in young patients with cryptogenic stroke.
4
Aim: The prevalence of hearing loss in patients with Fabry disease is still uncertain.
5
Despite enzyme replacement therapy, Fabry disease progresses with serious myocardial, cerebral and renal manifestations.
Russian
Portuguese
Spanish