methyl thiocyanate has been researched along with Cystic Fibrosis in 1 studies
*Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. [MeSH]
| 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 |
|---|---|
| Dřevínek, P; Dryahina, K; Nemec, A; Shestivska, V; Sovová, K; Spaněl, P | 1 |
1 other study(ies) available for methyl thiocyanate and Cystic Fibrosis
| Article | Year |
|---|---|
Quantification of methyl thiocyanate in the headspace of Pseudomonas aeruginosa cultures and in the breath of cystic fibrosis patients by selected ion flow tube mass spectrometry.
Topics: Adolescent; Biomarkers; Breath Tests; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Male; Mass Spectrometry; Pseudomonas aeruginosa; Pseudomonas Infections; Reproducibility of Results; Solid Phase Microextraction; Thiocyanates; Young Adult | 2011 |