carbostyril has been researched along with Paranasal Sinus Diseases in 4 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 | 3 (75.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Dansky, D; DiMango, E; Francis, SF; Gudis, D; Keating, C; Overdevest, J | 1 |
Hayes, D; McCoy, KS; Sheikh, SI | 1 |
Hayes, D; Johnson, T; Long, FR; McCoy, KS; Ryan-Wenger, NA; Sheikh, SI | 1 |
Berkhout, MC; Fokkens, WJ; Heijerman, HG; Sprij, AJ; Vreede, CL | 1 |
4 other study(ies) available for carbostyril and Paranasal Sinus Diseases
Article | Year |
---|---|
Effect of highly effective modulator treatment on sinonasal symptoms in cystic fibrosis.
Topics: Adult; Aminophenols; Benzodioxoles; Chloride Channel Agonists; Cystic Fibrosis; Drug Combinations; Female; Humans; Indoles; Male; Paranasal Sinus Diseases; Prospective Studies; Pyrazoles; Pyridines; Pyrrolidines; Quality of Life; Quinolones | 2021 |
Improvement of sinus disease in cystic fibrosis with ivacaftor therapy.
Topics: Acetates; Adult; Aminophenols; Androstadienes; Anti-Allergic Agents; Cyclopropanes; Cystic Fibrosis; Female; Fluticasone; Humans; Leukotriene Antagonists; Paranasal Sinus Diseases; Quinolines; Quinolones; Rhinitis, Allergic, Perennial; Sulfides; Treatment Outcome; Young Adult | 2014 |
Ivacaftor improves appearance of sinus disease on computerised tomography in cystic fibrosis patients with G551D mutation.
Topics: Adolescent; Adult; Aminophenols; Child; Cohort Studies; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Genotype; Humans; Male; Mutation; Paranasal Sinus Diseases; Quinolones; Tomography, X-Ray Computed; Treatment Outcome; Young Adult | 2015 |
Ivacaftor and sinonasal pathology in a cystic fibrosis patient with genotype deltaF508/S1215N.
Topics: Adolescent; Aminophenols; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA; Female; Forced Expiratory Volume; Genotype; Humans; Ion Transport; Mutation; Paranasal Sinus Diseases; Paranasal Sinuses; Quinolones; Tomography, X-Ray Computed | 2015 |