Rheological effects of hypertonic saline and sodium bicarbonate solutions on cystic fibrosis sputum in vitro
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R. Ambrus | P. Szabó-Révész | E. Csányi | M. Budai-Szűcs | S. Berkó | A. Kovács | Pongsiri Jaikumpun | A. Zsembery | A. Halász | Á. Zsembery
[1] M. Steward,et al. Antibacterial Effects of Bicarbonate in Media Modified to Mimic Cystic Fibrosis Sputum , 2020, International journal of molecular sciences.
[2] C. Murray,et al. Inhaled mannitol for cystic fibrosis. , 2020, The Cochrane database of systematic reviews.
[3] J. Cavanaugh,et al. Randomized controlled study of aerosolized hypertonic xylitol versus hypertonic saline in hospitalized patients with pulmonary exacerbation of cystic fibrosis. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[4] P. Quinton,et al. Safety, Tolerability, and Effects of Sodium Bicarbonate Inhalation in Cystic Fibrosis , 2019, Clinical Drug Investigation.
[5] R. Tarran,et al. Pathological mucus and impaired mucus clearance in cystic fibrosis patients result from increased concentration, not altered pH , 2018, European Respiratory Journal.
[6] P. Quinton,et al. Bicarbonate Inhibits Bacterial Growth and Biofilm Formation of Prevalent Cystic Fibrosis Pathogens , 2018, Front. Microbiol..
[7] L. Kang,et al. Cystic Fibrosis Sputum Rheology Correlates With Both Acute and Longitudinal Changes in Lung Function , 2018, Chest.
[8] C. Benden,et al. The many ways sputum flows – Dealing with high within-subject variability in cystic fibrosis sputum rheology , 2018, Respiratory Physiology & Neurobiology.
[9] P. Russo,et al. Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium Bicarbonate. , 2016, Journal of aerosol medicine and pulmonary drug delivery.
[10] R. Sadikot. Exacerbations of Cystic Fibrosis , 2016 .
[11] B. Antus. Oxidative Stress Markers in Sputum , 2016, Oxidative medicine and cellular longevity.
[12] Tiffany J Dwyer,et al. Inhaled mannitol for cystic fibrosis. , 2015, The Cochrane database of systematic reviews.
[13] Garry R. Cutting,et al. Cystic fibrosis genetics: from molecular understanding to clinical application , 2014, Nature Reviews Genetics.
[14] S. Donaldson,et al. Hypertonic saline for cystic fibrosis: worth its salt? , 2014, Expert review of respiratory medicine.
[15] P. Quinton,et al. Normal mucus formation requires cAMP‐dependent HCO3− secretion and Ca2+‐mediated mucin exocytosis , 2013, The Journal of physiology.
[16] R. Cone,et al. Barrier properties of mucus. , 2009, Advanced drug delivery reviews.
[17] P. Quinton. Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis , 2008, The Lancet.
[18] I. Doull,et al. Hypertonic saline inhalation in cystic fibrosis—salt in the wound, or sweet success? , 2007, Archives of Disease in Childhood.
[19] R. Kuhn,et al. Hypertonic Saline Treatment of Cystic Fibrosis , 2007, The Annals of pharmacotherapy.
[20] B. Rubin. Mucus structure and properties in cystic fibrosis. , 2007, Paediatric respiratory reviews.
[21] C. Goss,et al. Exacerbations in cystic fibrosis · 1: Epidemiology and pathogenesis , 2007, Thorax.
[22] S. Anderson,et al. Hyperosmolar agents and clearance of mucus in the diseased airway. , 2006, Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine.
[23] Mark R Elkins,et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. , 2006, The New England journal of medicine.
[24] M. King,et al. A new paradigm in respiratory hygiene: increasing the cohesivity of airway secretions to improve cough interaction and reduce aerosol dispersion , 2005, BMC pulmonary medicine.
[25] S. Anderson,et al. Inhaled mannitol for the treatment of mucociliary dysfunction in patients with bronchiectasis: Effect on lung function, health status and sputum , 2005, Respirology.
[26] B. Rubin. A superficial view of mucus and the cystic fibrosis defect , 1992, Pediatric pulmonology.
[27] J. Zahm,et al. Phospholipid composition and surface‐active properties of tracheobronchial secretions from patients with cystic fibrosis and chronic obstructive pulmonary diseases , 1992, Pediatric pulmonology.
[28] J. Zahm,et al. Rheology of sputum collected by a simple technique limiting salivary contamination. , 1984, The Journal of laboratory and clinical medicine.
[29] J. Kline,et al. Safety assessment of inhaled xylitol in subjects with cystic fibrosis. , 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[30] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[31] M. King. The role of mucus viscoelasticity in cough clearance. , 1987, Biorheology.