dexfenfluramine has been researched along with Telangiectasia, Hereditary Hemorrhagic 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 | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chaouat, A; Coulet, F; Favre, C; Humbert, M; Simonneau, G; Soubrier, F; Weitzenblum, E | 1 |
1 other study(ies) available for dexfenfluramine and Telangiectasia, Hereditary Hemorrhagic
Article | Year |
---|---|
Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension.
Topics: Adult; Antigens, CD; Dexfenfluramine; Endoglin; Female; Gene Deletion; Germ-Line Mutation; Heterozygote; Humans; Hypertension, Pulmonary; Pedigree; Receptors, Cell Surface; Serotonin Receptor Agonists; Telangiectasia, Hereditary Hemorrhagic; Vascular Cell Adhesion Molecule-1 | 2004 |