bezafibrate has been researched along with Glycogen Storage Disease Type II in 2 studies
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 | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Beller, M; Giese, AK; Gläser, A; Lukas, J; Pockrandt, AM; Pohlers, S; Rolfs, A; Runge, F; Seemann, S; Sharif, M; Zheng, C | 1 |
Angelini, C; Semplicini, C | 1 |
1 review(s) available for bezafibrate and Glycogen Storage Disease Type II
Article | Year |
---|---|
Metabolic myopathies: the challenge of new treatments.
Topics: Adult; Animals; Bezafibrate; Carnitine O-Palmitoyltransferase; Child; Early Diagnosis; Enzyme Replacement Therapy; Fatty Acids; Glycogen Storage Disease Type II; Glycogen Storage Disease Type V; Humans; Hypolipidemic Agents; Infant; Oxidation-Reduction | 2010 |
1 other study(ies) available for bezafibrate and Glycogen Storage Disease Type II
Article | Year |
---|---|
Enzyme enhancers for the treatment of Fabry and Pompe disease.
Topics: 1-Deoxynojirimycin; Acetylcysteine; alpha-Galactosidase; alpha-Glucosidases; Ambroxol; Bezafibrate; Enzyme Activators; Fabry Disease; Gene Expression; Glycogen Storage Disease Type II; HEK293 Cells; Humans; Leupeptins; Lysosomes; Pioglitazone; Plasmids; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Stability; Recombinant Proteins; Thiazolidinediones; Transfection | 2015 |