lopinavir has been researched along with Lipodystrophy, Familial Partial in 1 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Araújo-Vilar, D; Fong, LG; Sánchez-Iglesias, S; Tu, Y; Young, SG | 1 |
1 other study(ies) available for lopinavir and Lipodystrophy, Familial Partial
| Article | Year |
|---|---|
LMNA missense mutations causing familial partial lipodystrophy do not lead to an accumulation of prelamin A.
Topics: Base Sequence; Fibroblasts; Humans; Lamin Type A; Lipodystrophy, Familial Partial; Lopinavir; Mutation, Missense | 2016 |