ursodeoxycholic acid has been researched along with alpha 1-Antitrypsin Deficiency 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Blomenkamp, K; Fickert, P; Marcus, N; Tang, Y; Teckman, J; Trauner, M | 1 |
| Bernard, O; Broué, P; Dabadie, A; Ducot, B; Jacquemin, E; Lachaux, A; Lykavieris, P; Sarles, J | 1 |
2 other study(ies) available for ursodeoxycholic acid and alpha 1-Antitrypsin Deficiency
| Article | Year |
|---|---|
Autophagy induced by exogenous bile acids is therapeutic in a model of α-1-AT deficiency liver disease.
Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Animals; Autophagy; Cells, Cultured; Deoxycholic Acid; Disease Models, Animal; Genetic Predisposition to Disease; Humans; Liver; Liver Cirrhosis; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Phenotype; Transfection; Ursodeoxycholic Acid | 2016 |
Liver disease associated with ZZ alpha1-antitrypsin deficiency and ursodeoxycholic acid therapy in children.
Topics: Alanine Transaminase; alpha 1-Antitrypsin Deficiency; Aspartate Aminotransferases; Bilirubin; Child; Child, Preschool; Female; Follow-Up Studies; gamma-Glutamyltransferase; Humans; Infant; Infant, Newborn; Liver Diseases; Liver Function Tests; Male; Phenotype; Recurrence; Retrospective Studies; Ursodeoxycholic Acid | 2008 |