Page last updated: 2024-09-03

hippurin and Fabry Disease

hippurin has been researched along with Fabry Disease in 1 studies

*Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. [MeSH]

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baas, MC; Bemelman, FJ; Hollak, CE; Krediet, RT; Rombach, SM; ten Berge, IJ1

Other Studies

1 other study(ies) available for hippurin and Fabry Disease

ArticleYear
The value of estimated GFR in comparison to measured GFR for the assessment of renal function in adult patients with Fabry disease.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2010, Volume: 25, Issue:8

    Topics: Adolescent; Adult; Aged; Biomarkers; Creatinine; Cystatin C; Fabry Disease; Female; Glomerular Filtration Rate; Humans; Intramolecular Oxidoreductases; Kidney; Kidney Function Tests; Lipocalins; Male; Middle Aged; Sterols; Young Adult

2010