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Significats de fabry disease en anglès

rus
болезнь фабри
portuguès
doença de fabry
espanyol
enfermedad de fabry
català
malaltia d'anderson-fabry
Wikidata

Rare human genetic lysosomal storage disorder.

      Termes relacionats
      malaltia d'anderson-fabry
      Sinònims
      Examples for "fd"
      Examples for "fd"
      1
      The fd coat protein was purified by gel chromatography of the SDA solubilized virus.
      Pubmed
      2
      These findings make fd bacteriophage a valuable tool for immunization without administering exogenous adjuvants.
      Pubmed
      3
      In order to investigate the mechanisms of this activity, RNA-Sequencing of fd-pulsed dendritic cells was performed.
      Pubmed
      4
      The minor coat proteins of the filamentous bacteriophage fl and fd have been isolated and characterized.
      Pubmed
      5
      These findings may guide program planning for future FD to support IPE.
      Pubmed
      1
      Recent advances in enzyme replacement therapy can reverse the storage of glycosphingolipids in Fabry's disease.
      Pubmed
      2
      The diagnosis of Fabry's disease was made by the absence of plasma alpha-galactosidase A activity.
      Pubmed
      3
      Thus, in patients with cardiac hypertrophy, it is important to differentiate Fabry's disease from other causes of hypertrophy.
      Pubmed
      4
      This was a very rare case of subclinical Fabry's disease coexistent with cholesterol crystal embolization, mimicking pulmonary-renal syndrome.
      Pubmed
      Ús de fabry disease en anglès
      1
      Tinnitus may be an earlier symptom than previously thought in Fabry disease.
      Pubmed
      2
      This paper examines hearing loss in a group of young patients with Fabry disease.
      Pubmed
      3
      Objective: To assess the prevalence of Fabry disease in young patients with cryptogenic stroke.
      Pubmed
      4
      Aim: The prevalence of hearing loss in patients with Fabry disease is still uncertain.
      Pubmed
      5
      Despite enzyme replacement therapy, Fabry disease progresses with serious myocardial, cerebral and renal manifestations.
      Pubmed
      6
      Moreover, Fabry disease could not be ruled out as the clinical diagnosis of ESKD.
      Pubmed
      7
      The most appropriate time for screening for Fabry disease (FD) is school age.
      Pubmed
      8
      Eight biochemically proven Fabry disease patients (from four families) were included.
      Pubmed
      9
      Objective: Fabry disease is a rare X-linked inherited lysosomal storage disorder affecting multiple organ systems.
      Pubmed
      10
      PRX-102 or alpha-GAL-A is an enzyme replacement therapy product for the treatment of Fabry disease.
      Reuters
      11
      The pathological study of the cardiac biopsy sample showed no characteristic findings of Fabry disease.
      Pubmed
      12
      Patients with Fabry disease lack a specific enzyme and the condition is fatal without lifelong treatment.
      Reuters
      13
      Fabry disease was confirmed by family history and a positive enzyme test, and ERT was commenced.
      Pubmed
      14
      This study was designed to determine the prevalence rate of Fabry disease in Japanese dialysis patients.
      Pubmed
      15
      We screened for Fabry disease by measurement of alpha-galactosidase A and beta-glucuronidase activity on blood spot.
      Pubmed
      16
      To investigate the effects of purified alpha-gal A, 10 patients with Fabry disease received a single i.v.
      Pubmed
      Translations for fabry disease