migalastat has been researched along with Hypertrophy, Left Ventricular 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 |
---|---|
Cui, G; Huang, J; Wang, DW; Zeng, H; Zhou, C; Zhou, Q | 1 |
Amartino, H; Banikazemi, M; Barlow, C; Barth, J; Benjamin, ER; Bichet, DG; Bratkovic, D; Castelli, J; Charrow, J; Dasouki, M; Ezgu, F; Feldt-Rasmussen, U; Feliciani, C; Finegold, D; Germain, DP; Giraldo, P; Giugliani, R; Goker-Alpan, O; Hughes, DA; Johnson, F; Jovanovic, A; Kirk, J; Lockhart, DJ; Longo, N; Lourenco, CM; Ludington, E; Nedd, K; Nicholls, K; Packman, S; Schiffmann, R; Scott, CR; Shankar, SP; Sharaf El Din, U; Skuban, N; Torra, R; Tuffaha, A; Viereck, C; Waldek, S; Wilcox, WR; Yu, J | 1 |
1 trial(s) available for migalastat and Hypertrophy, Left Ventricular
Article | Year |
---|---|
Treatment of Fabry's Disease with the Pharmacologic Chaperone Migalastat.
Topics: 1-Deoxynojirimycin; Adolescent; Adult; Aged; alpha-Galactosidase; Diarrhea; Double-Blind Method; Fabry Disease; Female; Glomerular Filtration Rate; Heart Ventricles; Humans; Hypertrophy, Left Ventricular; Kidney; Male; Middle Aged; Mutation; Trihexosylceramides; Ultrasonography; Young Adult | 2016 |
1 other study(ies) available for migalastat and Hypertrophy, Left Ventricular
Article | Year |
---|---|
Identification of a novel loss-of-function mutation of the GLA gene in a Chinese Han family with Fabry disease.
Topics: 1-Deoxynojirimycin; Adult; Aged; alpha-Galactosidase; Asian People; Base Sequence; Child; Exons; Fabry Disease; Female; Gene Expression; Glycolipids; HEK293 Cells; Humans; Hypertrophy, Left Ventricular; Kidney Failure, Chronic; Loss of Function Mutation; Male; Middle Aged; Pedigree; Phenotype | 2018 |