Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
about
Cystic Fibrosis: Lessons from the Sweat GlandSodium channel blockers for cystic fibrosisSodium channel blockers for cystic fibrosisTiming of hypertonic saline inhalation for cystic fibrosisTiming of hypertonic saline inhalation for cystic fibrosisSodium channel blockers for cystic fibrosisThe epithelial anion transporter pendrin is induced by allergy and rhinovirus infection, regulates airway surface liquid, and increases airway reactivity and inflammation in an asthma modelEpithelial Anion Transport as Modulator of Chemokine SignalingCurrent and future treatment options for cystic fibrosis lung disease: latest evidence and clinical implicationsOptimising inhaled mannitol for cystic fibrosis in an adult populationInhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and functionStenotrophomonas maltophilia: an emerging global opportunistic pathogenThe Evolution of Cystic Fibrosis CareMethod for quantitative study of airway functional microanatomy using micro-optical coherence tomographyA physiologically-motivated compartment-based model of the effect of inhaled hypertonic saline on mucociliary clearance and liquid transport in cystic fibrosisAirway hydration and COPDNebulized hypertonic saline decreases IL-8 in sputum of patients with cystic fibrosisResponse of Differentiated Human Airway Epithelia to Alcohol Exposure and Klebsiella Pneumoniae ChallengeFunctionalized positive nanoparticles reduce mucin swelling and dispersionBdlA, DipA and induced dispersion contribute to acute virulence and chronic persistence of Pseudomonas aeruginosaModeling and Simulation of Mucus Flow in Human Bronchial Epithelial Cell Cultures - Part I: Idealized Axisymmetric Swirling FlowAdvances toward the elucidation of hypertonic saline effects on Pseudomonas aeruginosa from cystic fibrosis patientsCFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epitheliumBarriers to inhaled gene therapy of obstructive lung diseases: A reviewNoninvasive real-time measurement of nasal mucociliary clearance in mice by pinhole gamma scintigraphy.Non-invasive airway health assessment: synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo.Little Cigars are More Toxic than Cigarettes and Uniquely Change the Airway Gene and Protein Expression.Clinical practice and genetic counseling for cystic fibrosis and CFTR-related disorders.Usefulness of sputum induction with hypertonic saline in a real clinical practice for bacteriological yields of active pulmonary tuberculosisENaC-mediated effects assessed by MRI in a rat model of hypertonic saline-induced lung hydration.Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in cystic fibrosisDetermination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection.Cystic fibrosis: exploiting its genetic basis in the hunt for new therapiesAirway mucus function and dysfunction.Vagal control of mucociliary clearance in murine lungs: a study in a chronic preparation.Airway-rehydrating agents for the treatment of cystic fibrosis: past, present, and future.Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short-term tolerability, adherence, and safety.Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway.Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung.Common gene therapy viral vectors do not efficiently penetrate sputum from cystic fibrosis patients.
P2860
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P2860
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@en
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@nl
type
label
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@en
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@nl
prefLabel
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@en
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@nl
P2093
P356
P1476
Mucus clearance and lung function in cystic fibrosis with hypertonic saline.
@en
P2093
Kirby L Zeman
Michael R Knowles
Richard C Boucher
Robert Tarran
Scott H Donaldson
William D Bennett
P304
P356
10.1056/NEJMOA043891
P407
P577
2006-01-01T00:00:00Z