Page last updated: 2024-10-19

phosphorylcholine and Fabry Disease

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.

Research

Studies (1)

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

Authors

AuthorsStudies
Fujiwaki, T1
Tasaka, M1
Takahashi, N1
Kobayashi, H1
Murakami, Y1
Shimada, T1
Yamaguchi, S1

Other Studies

1 other study available for phosphorylcholine and Fabry Disease

ArticleYear
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
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2006, Feb-17, Volume: 832, Issue:1

    Topics: Chromatography, Thin Layer; Fabry Disease; Heart Valves; Humans; Male; Middle Aged; Phosphorylcholin

2006