alpha-aminopyridine has been researched along with Orphan Diseases 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 |
---|---|
Becq, F; Callebaut, I; Jollivet Souchet, M; Prasad, R; Sharma, H | 1 |
Bast, A; Bootsma, HP; Deneer, V; Drent, M | 1 |
2 other study(ies) available for alpha-aminopyridine and Orphan Diseases
Article | Year |
---|---|
Function, pharmacological correction and maturation of new Indian CFTR gene mutations.
Topics: Aminopyridines; Benzodioxoles; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Gene Expression Regulation; Humans; India; Infertility, Male; Male; Male Urogenital Diseases; Mutation, Missense; Rare Diseases; Sampling Studies; Sexual Maturation; Vas Deferens | 2015 |
Repositioning 'old' drugs to treat rare diseases: arguing from the mechanism of action.
Topics: Administration, Oral; Aminopyridines; Benzamides; Cyclopropanes; Drug Repositioning; Evidence-Based Medicine; Female; Histiocytosis, Langerhans-Cell; Humans; Middle Aged; Orphan Drug Production; Phosphodiesterase 4 Inhibitors; Rare Diseases; Tomography, X-Ray Computed; Treatment Outcome | 2016 |