Page last updated: 2024-08-21

thiazolidines and Congenital Disorders of Glycosylation

thiazolidines has been researched along with Congenital Disorders of Glycosylation in 2 studies

Research

Studies (2)

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 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Brucker, W; Cassiman, D; Edmondson, AC; Garapati, K; Ghesquière, B; Johnsen, C; Kozicz, T; Krzysciak, W; Lam, C; Larson, A; Ligezka, AN; McGovern, RM; Mercimek-Andrews, S; Morava, E; Muthusamy, K; Oglesbee, D; Pandey, A; Perlstein, EO; Preston, G; Radenkovic, S; Ranatunga, W; Raymond, K; Reid, JM; Saraswat, M; Witters, P; Yanaihara, H1
DiPrimio, N; Iyer, S; Lao, J; Morava, E; Murthy, K; Parton, Z; Perlstein, EO; Preston, G; Sam, FS; Tsang, H; Verheijen, J1

Other Studies

2 other study(ies) available for thiazolidines and Congenital Disorders of Glycosylation

ArticleYear
Sorbitol Is a Severity Biomarker for PMM2-CDG with Therapeutic Implications.
    Annals of neurology, 2021, Volume: 90, Issue:6

    Topics: Adolescent; Adult; Aged; Biomarkers; Child; Child, Preschool; Congenital Disorders of Glycosylation; Enzyme Inhibitors; Female; Glycosylation; Humans; Infant; Male; Middle Aged; Patient Acuity; Phosphotransferases (Phosphomutases); Prognosis; Rhodanine; Sorbitol; Thiazolidines; Young Adult

2021
Repurposing the aldose reductase inhibitor and diabetic neuropathy drug epalrestat for the congenital disorder of glycosylation PMM2-CDG.
    Disease models & mechanisms, 2019, 11-11, Volume: 12, Issue:11

    Topics: Aldehyde Reductase; Animals; Cells, Cultured; Congenital Disorders of Glycosylation; Diabetic Neuropathies; Disease Models, Animal; Drug Repositioning; Endoplasmic Reticulum Stress; Fibroblasts; Glycosylation; Humans; Nematoda; Phosphotransferases (Phosphomutases); Polyphenols; Rhodanine; Thiazolidines

2019