phosphorylcholine has been researched along with Fabry Disease in 1 studies
Phosphorylcholine: Calcium and magnesium salts used therapeutically in hepatobiliary dysfunction.
phosphocholine : The phosphate of choline; and the parent compound of the phosphocholine family.
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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fujiwaki, T | 1 |
Tasaka, M | 1 |
Takahashi, N | 1 |
Kobayashi, H | 1 |
Murakami, Y | 1 |
Shimada, T | 1 |
Yamaguchi, S | 1 |
1 other study available for phosphorylcholine and Fabry Disease
Article | Year |
---|---|
Quantitative evaluation of sphingolipids using delayed extraction matrix-assisted laser desorption ionization time-of-flight mass spectrometry with sphingosylphosphorylcholine as an internal standard. Practical application to cardiac valves from a patient
Topics: Chromatography, Thin Layer; Fabry Disease; Heart Valves; Humans; Male; Middle Aged; Phosphorylcholin | 2006 |