Page last updated: 2024-11-03

pyrimethamine and Adult Sandhoff Disease

pyrimethamine has been researched along with Adult Sandhoff Disease in 1 studies

Maloprim: contains above 2 cpds

Research Excerpts

ExcerptRelevanceReference
"Sandhoff disease is an autosomal recessive inherited disorder resulting from β-hexosaminidase deficiency and characterized by large accumulation of GM2 ganglioside in brain."2.50Chaperone 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)

Research

Studies (1)

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

Authors

AuthorsStudies
Chiricozzi, E1
Niemir, N1
Aureli, M1
Magini, A1
Loberto, N1
Prinetti, A1
Bassi, R1
Polchi, A1
Emiliani, C1
Caillaud, C1
Sonnino, S1

Reviews

1 review available for pyrimethamine and Adult Sandhoff Disease

ArticleYear
Chaperone therapy for GM2 gangliosidosis: effects of pyrimethamine on β-hexosaminidase activity in Sandhoff fibroblasts.
    Molecular neurobiology, 2014, Volume: 50, Issue:1

    Topics: Fibroblasts; Hexosaminidase B; Humans; Molecular Chaperones; Pyrimethamine; Sandhoff Disease

2014