urea has been researched along with Cystic Fibrosis of Pancreas in 33 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Intravenous colistin is an effective treatment for Pseudomonas aeruginosa associated pulmonary exacerbations in patients with cystic fibrosis." | 9.08 | Intravenous colistin sulphomethate in acute respiratory exacerbations in adult patients with cystic fibrosis. ( Conway, SP; Etherington, C; Goldman, MH; Pond, MN; Robey, HL; Watson, A, 1997) |
| "Urea excretion was maximal in the evening at approximately 2000 and minimal at 0800, whereas the [15N]urea enrichment was maximal at about 0800 and minimal at 2000." | 5.27 | Diurnal variation in urine [15N]urea content, estimates of whole body protein turnover, and isotope recycling in healthy meal-fed children with cystic fibrosis. ( Parsons, HG; Pencharz, PB; Wood, MM, 1983) |
| " We utilized mass spectrometry to measure EBC purine biomarkers adenosine and AMP plus urea to control for dilutional variability in two studies: 1) a cross-sectional analysis of 28 healthy, 40 cystic fibrosis (CF), and 11 asthmatic children; and 2) a longitudinal analysis of 26 CF children before and after treatment of a pulmonary exacerbation." | 5.14 | Mass spectrometric analysis of biomarkers and dilution markers in exhaled breath condensate reveals elevated purines in asthma and cystic fibrosis. ( Boucher, RC; Boysen, G; Collins, LB; Esther, CR; Ghio, AJ; Olsen, BM; Swenberg, JW, 2009) |
| "Intravenous colistin is an effective treatment for Pseudomonas aeruginosa associated pulmonary exacerbations in patients with cystic fibrosis." | 5.08 | Intravenous colistin sulphomethate in acute respiratory exacerbations in adult patients with cystic fibrosis. ( Conway, SP; Etherington, C; Goldman, MH; Pond, MN; Robey, HL; Watson, A, 1997) |
| "In asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis, increased arginase activity in the airways may contribute to obstruction and hyperresponsiveness of the airways by inducing a reduction in the production of bronchodilatory nitric oxide (NO) that results from its competition with constitutive (cNOS) and inducible (iNOS) NO synthases for their common substrate." | 2.44 | Arginase and pulmonary diseases. ( Maarsingh, H; Meurs, H; Pera, T, 2008) |
| "Urea is a non-volatile molecule ex vivo and EBC urea depends on its concentrations in plasma." | 1.35 | Urea in exhaled breath condensate of uraemics and patients with chronic airway diseases. ( Acampa, O; Andreoli, R; Bertorelli, G; Corradi, M; David, S; Folesani, G; Franchini, I; Goldoni, M; Manini, P, 2008) |
| "The role of these factors in the pulmonary disease associated with cystic fibrosis is not clear." | 1.28 | Pathogenic factors of Pseudomonas cepacia isolates from patients with cystic fibrosis. ( Gessner, AR; Mortensen, JE, 1990) |
| "Urea excretion was maximal in the evening at approximately 2000 and minimal at 0800, whereas the [15N]urea enrichment was maximal at about 0800 and minimal at 2000." | 1.27 | Diurnal variation in urine [15N]urea content, estimates of whole body protein turnover, and isotope recycling in healthy meal-fed children with cystic fibrosis. ( Parsons, HG; Pencharz, PB; Wood, MM, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (39.39) | 18.7374 |
| 1990's | 2 (6.06) | 18.2507 |
| 2000's | 10 (30.30) | 29.6817 |
| 2010's | 6 (18.18) | 24.3611 |
| 2020's | 2 (6.06) | 2.80 |
| Authors | Studies |
|---|---|
| Rachel, M | 1 |
| Galiniak, S | 1 |
| Biesiadecki, M | 1 |
| Gala-Błądzińska, A | 1 |
| Kumar, PA | 1 |
| Pradeep, A | 1 |
| Nair, BKG | 1 |
| Babu, TGS | 1 |
| Suneesh, PV | 1 |
| Spoletini, G | 1 |
| Kennedy, M | 1 |
| Flint, L | 1 |
| Graham, T | 1 |
| Etherington, C | 2 |
| Shaw, N | 1 |
| Whitaker, P | 1 |
| Denton, M | 1 |
| Clifton, I | 1 |
| Peckham, D | 1 |
| Monge, ME | 1 |
| Pérez, JJ | 1 |
| Dwivedi, P | 1 |
| Zhou, M | 1 |
| McCarty, NA | 1 |
| Stecenko, AA | 1 |
| Fernández, FM | 1 |
| Drzymała-Czy, S | 1 |
| Stawinska-Witoszynska, B | 1 |
| Mądry, E | 1 |
| Krzywinska-Wiewiórowska, M | 1 |
| Szczepanik, M | 1 |
| Walkowiak, J | 1 |
| Kwiecien, J | 1 |
| Esther, CR | 4 |
| Hill, DB | 1 |
| Button, B | 1 |
| Shi, S | 1 |
| Jania, C | 1 |
| Duncan, EA | 1 |
| Doerschuk, CM | 1 |
| Chen, G | 1 |
| Ranganathan, S | 1 |
| Stick, SM | 1 |
| Boucher, RC | 3 |
| Folesani, G | 1 |
| Corradi, M | 1 |
| Goldoni, M | 1 |
| Manini, P | 1 |
| Acampa, O | 1 |
| Andreoli, R | 1 |
| Bertorelli, G | 1 |
| David, S | 1 |
| Franchini, I | 1 |
| Boysen, G | 2 |
| Olsen, BM | 2 |
| Collins, LB | 2 |
| Ghio, AJ | 1 |
| Swenberg, JW | 1 |
| Sovtic, AD | 1 |
| Minic, PB | 1 |
| Kosutic, J | 1 |
| Markovic-Sovtic, GP | 1 |
| Gajic, MB | 1 |
| Lin, FC | 1 |
| Fine, J | 1 |
| Aitken, ML | 2 |
| Greene, KE | 1 |
| Tonelli, MR | 2 |
| Burns, JL | 2 |
| Emerson, JC | 1 |
| Goss, CH | 1 |
| Gibson, RL | 1 |
| Russo, MA | 1 |
| Hogenauer, C | 1 |
| Coates, SW | 1 |
| Santa Ana, CA | 1 |
| Porter, JL | 1 |
| Rosenblatt, RL | 1 |
| Emmett, M | 1 |
| Fordtran, JS | 1 |
| RICHTERICH, R | 3 |
| FRIOLET, B | 3 |
| FLEISHER, DS | 1 |
| DIGEORGE, AM | 1 |
| AUERBACH, VH | 1 |
| HUANG, NN | 1 |
| BARNESS, LA | 1 |
| Geukers, VG | 1 |
| Oudshoorn, JH | 1 |
| Taminiau, JA | 1 |
| van der Ent, CK | 1 |
| Schilte, P | 1 |
| Ruiter, AF | 1 |
| Ackermans, MT | 1 |
| Endert, E | 1 |
| Jonkers-Schuitema, CF | 1 |
| Heymans, HS | 1 |
| Sauerwein, HP | 1 |
| Jasin, HM | 1 |
| Swenberg, JA | 1 |
| Maarsingh, H | 1 |
| Pera, T | 1 |
| Meurs, H | 1 |
| Mandel, ID | 1 |
| Kutscher, A | 1 |
| Denning, CR | 1 |
| Thompson, RH | 1 |
| Zegarelli, EV | 1 |
| Emrich, HM | 2 |
| Stoll, E | 2 |
| Colombo, JP | 2 |
| Rossi, E | 2 |
| Mowat, AP | 1 |
| Parsons, HG | 1 |
| Wood, MM | 1 |
| Pencharz, PB | 1 |
| Conway, SP | 1 |
| Pond, MN | 1 |
| Watson, A | 1 |
| Robey, HL | 1 |
| Goldman, MH | 1 |
| Henig, NR | 1 |
| Pier, MV | 1 |
| Koerbin, G | 1 |
| Taylor, L | 1 |
| Dutton, J | 1 |
| Marshall, K | 1 |
| Low, P | 1 |
| Potter, JM | 1 |
| Kirkham, S | 1 |
| Sheehan, JK | 1 |
| Knight, D | 1 |
| Richardson, PS | 1 |
| Thornton, DJ | 1 |
| Allars, HM | 2 |
| Blomfield, J | 2 |
| Rush, AR | 2 |
| Brown, JM | 2 |
| Cockayne, DJ | 1 |
| Van Lennep, EW | 1 |
| Gessner, AR | 1 |
| Mortensen, JE | 1 |
| Novelli, G | 1 |
| Mannello, F | 1 |
| Pierotti, C | 1 |
| Antonelli, M | 1 |
| Dallapiccola, B | 1 |
| Goodchild, MC | 1 |
| Sagaró, E | 1 |
| Brown, GA | 1 |
| Cruchley, PM | 1 |
| Jukes, HR | 1 |
| Anderson, CM | 1 |
| Slegers, JF | 1 |
| Mei, V | 1 |
| Comellini, L | 1 |
| Secciani, L | 1 |
| Paolucci, G | 1 |
2 reviews available for urea and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Arginase and pulmonary diseases.
Topics: Animals; Arginase; Arginine; Asthma; Cystic Fibrosis; Disease Models, Animal; Humans; Hypertension, | 2008 |
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Ch | 1982 |
5 trials available for urea and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Mass spectrometric analysis of biomarkers and dilution markers in exhaled breath condensate reveals elevated purines in asthma and cystic fibrosis.
Topics: Adenosine; Adenosine Monophosphate; Adolescent; Asthma; Biomarkers; Breath Tests; Child; Child, Pres | 2009 |
Exhaled breath condensate adenosine tracks lung function changes in cystic fibrosis.
Topics: Adenosine; Adolescent; Adult; Biomarkers; Child; Cystic Fibrosis; Female; Humans; Interleukin-8; Mal | 2013 |
Short-term protein intake and stimulation of protein synthesis in stunted children with cystic fibrosis.
Topics: Body Height; Carbon Isotopes; Child; Child Development; Child Nutritional Physiological Phenomena; C | 2005 |
Intravenous colistin sulphomethate in acute respiratory exacerbations in adult patients with cystic fibrosis.
Topics: Acute Disease; Adult; Analysis of Variance; Anti-Bacterial Agents; Colistin; Creatinine; Cystic Fibr | 1997 |
Comparative trial of pancrex V forte and nutrizym in treatment of malabsorption in cystic fibrosis.
Topics: Adolescent; Amylases; Bromelains; Child; Child, Preschool; Clinical Trials as Topic; Cystic Fibrosis | 1974 |
26 other studies available for urea and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Renal Function in Patients with Cystic Fibrosis: A Single-Center Study.
Topics: Biomarkers; Creatinine; Cystatin C; Cystic Fibrosis; Female; Glomerular Filtration Rate; Humans; Kid | 2022 |
Silver-manganese nanocomposite modified screen-printed carbon electrode in the fabrication of an electrochemical, disposable biosensor strip for cystic fibrosis.
Topics: Biosensing Techniques; Carbon; Chlorides; Cystic Fibrosis; Electrodes; Humans; Manganese; Manganese | 2022 |
Intravenous fosfomycin for pulmonary exacerbation of cystic fibrosis: Real life experience of a large adult CF centre.
Topics: Administration, Intravenous; Adult; Anti-Bacterial Agents; C-Reactive Protein; Creatinine; Cystic Fi | 2018 |
Ion mobility and liquid chromatography/mass spectrometry strategies for exhaled breath condensate glucose quantitation in cystic fibrosis studies.
Topics: Biomarkers; Breath Tests; Chromatography, Liquid; Cystic Fibrosis; Diabetes Complications; Glucose; | 2013 |
Non-invasive detection of Helicobacter pylori in cystic fibrosis--the fecal test vs. the urea breath test.
Topics: Adolescent; Adult; Antigens, Bacterial; Breath Tests; Child; Child, Preschool; Cystic Fibrosis; Fece | 2014 |
Sialic acid-to-urea ratio as a measure of airway surface hydration.
Topics: Animals; Body Fluids; Child, Preschool; Cystic Fibrosis; Demography; Epithelial Cells; Female; Human | 2017 |
Urea in exhaled breath condensate of uraemics and patients with chronic airway diseases.
Topics: Adult; Asthma; Breath Tests; Cystic Fibrosis; Female; Humans; Male; Middle Aged; Pulmonary Disease, | 2008 |
Static hyperinflation is associated with decreased peak exercise performance in children with cystic fibrosis.
Topics: Adolescent; Blood Gas Analysis; Carbamide Peroxide; Child; Cystic Fibrosis; Exercise Test; Exercise | 2013 |
Analysis of sequential aliquots of hypertonic saline solution-induced sputum from clinically stable patients with cystic fibrosis.
Topics: Adult; Biomarkers; Cell Count; Colony Count, Microbial; Cystic Fibrosis; Female; Humans; Interleukin | 2003 |
Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.
Topics: Adult; Bicarbonates; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator | 2003 |
THE EFFECT OF ACETAZOLAMIDE ON SWEAT ELECTROLYTES IN MUCOVISCIDOSIS.
Topics: Acetazolamide; Carbonic Anhydrases; Child; Chlorides; Cystic Fibrosis; Electrolytes; Humans; Iontoph | 1963 |
PROTEIN METABOLISM IN CYSTIC FIBROSIS OF THE PANCREAS.
Topics: Ammonia; Cystic Fibrosis; Feces; Humans; Infant; Nitrogen; Peptides; Proteins; Urea; Urine | 1964 |
A mass spectrometric method to simultaneously measure a biomarker and dilution marker in exhaled breath condensate.
Topics: Adenosine; Adenosine Monophosphate; Biomarkers; Breath Tests; Bronchi; Child; Chromatography, High P | 2008 |
Salivary studies in cystic fibrosis.
Topics: Adolescent; Ammonia; Amylases; Calcium; Carbohydrates; Child; Chlorides; Cystic Fibrosis; Electropho | 1967 |
Excretion of different substances in the sweat of children with cystic fibrosis and controls.
Topics: Aldosterone; Calcium; Child; Chlorides; Creatinine; Cystic Fibrosis; Humans; Lactates; Male; Sodium; | 1967 |
Diurnal variation in urine [15N]urea content, estimates of whole body protein turnover, and isotope recycling in healthy meal-fed children with cystic fibrosis.
Topics: Amino Acids; Child; Circadian Rhythm; Cystic Fibrosis; Dietary Proteins; Female; Humans; Male; Nitro | 1983 |
Sputum induction as a research tool for sampling the airways of subjects with cystic fibrosis.
Topics: Adult; Analysis of Variance; Bronchoalveolar Lavage; Bronchoalveolar Lavage Fluid; Cystic Fibrosis; | 2001 |
Aminoglycoside interference with the Dade Behring pyrogallol red-molybdate method for the measurement of total urine protein.
Topics: Aminoglycosides; Coloring Agents; Cystic Fibrosis; Humans; Indicators and Reagents; Molybdenum; Pyro | 2001 |
Heterogeneity of airways mucus: variations in the amounts and glycoforms of the major oligomeric mucins MUC5AC and MUC5B.
Topics: Asthma; Blotting, Western; Cystic Fibrosis; Dose-Response Relationship, Drug; Electrophoresis, Agar | 2002 |
Colloid and crystal formation in parotid saliva of cystic fibrosis patients and non-cystic fibrosis subjects. I. Physicochemistry.
Topics: Adolescent; Adult; Calcium; Chemical Phenomena; Chemistry, Physical; Child; Cold Temperature; Colloi | 1976 |
Colloid and crystal formation in parotid saliva of cystic fibrosis patients and non-cystic fibrosis subjects. II. Electron microscopy and electrophoresis.
Topics: Adolescent; Adult; Calcium Phosphates; Child; Cold Temperature; Colloids; Crystallization; Cystic Fi | 1976 |
Pathogenic factors of Pseudomonas cepacia isolates from patients with cystic fibrosis.
Topics: Amino Acids; Catalase; Cystic Fibrosis; Cytotoxins; Endopeptidases; Glycoside Hydrolases; Hemolysis; | 1990 |
Protocol for prenatal diagnosis of cystic fibrosis based on studies of alkaline phosphatase isoenzymes.
Topics: Alkaline Phosphatase; Amniotic Fluid; Clinical Enzyme Tests; Cystic Fibrosis; Electrophoresis, Polya | 1988 |
Sweat composition in relation to rate of sweating in patients with cystic fibrosis of the pancreas.
Topics: Calcium; Chlorides; Creatinine; Cystic Fibrosis; Glucose; Humans; Hydrogen-Ion Concentration; Lactat | 1968 |
The influx and outflux of sodium in the sweat-gland.
Topics: Cystic Fibrosis; Humans; Secretory Rate; Sodium; Sweat; Sweat Glands; Urea | 1966 |
[Total osmolarity and principal osmoactive constituents of sweat in subjects with mucoviscidosis and their families].
Topics: Adult; Child, Preschool; Chlorides; Cystic Fibrosis; Humans; Infant; Lactates; Middle Aged; Potassiu | 1966 |