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]
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Baas, MC; Bemelman, FJ; Hollak, CE; Krediet, RT; Rombach, SM; ten Berge, IJ | 1 |
1 other study(ies) available for hippurin and Fabry Disease
Article | Year |
---|---|
The value of estimated GFR in comparison to measured GFR for the assessment of renal function in adult patients with Fabry disease.
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 |