pyrimethamine has been researched along with Adult Sandhoff Disease in 1 studies
Maloprim: contains above 2 cpds
Excerpt | Relevance | Reference |
---|---|---|
"Sandhoff disease is an autosomal recessive inherited disorder resulting from β-hexosaminidase deficiency and characterized by large accumulation of GM2 ganglioside in brain." | 2.50 | Chaperone therapy for GM2 gangliosidosis: effects of pyrimethamine on β-hexosaminidase activity in Sandhoff fibroblasts. ( Aureli, M; Bassi, R; Caillaud, C; Chiricozzi, E; Emiliani, C; Loberto, N; Magini, A; Niemir, N; Polchi, A; Prinetti, A; Sonnino, S, 2014) |
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 |
---|---|
Chiricozzi, E | 1 |
Niemir, N | 1 |
Aureli, M | 1 |
Magini, A | 1 |
Loberto, N | 1 |
Prinetti, A | 1 |
Bassi, R | 1 |
Polchi, A | 1 |
Emiliani, C | 1 |
Caillaud, C | 1 |
Sonnino, S | 1 |
1 review available for pyrimethamine and Adult Sandhoff Disease
Article | Year |
---|---|
Chaperone therapy for GM2 gangliosidosis: effects of pyrimethamine on β-hexosaminidase activity in Sandhoff fibroblasts.
Topics: Fibroblasts; Hexosaminidase B; Humans; Molecular Chaperones; Pyrimethamine; Sandhoff Disease | 2014 |