[HTML][HTML] Physicochemical properties of mucus and their impact on transmucosal drug delivery
Mucus is a selective barrier to particles and molecules, preventing penetration to the
epithelial surface of mucosal tissues. Significant advances in transmucosal drug delivery …
epithelial surface of mucosal tissues. Significant advances in transmucosal drug delivery …
Stenotrophomonas maltophilia: an emerging global opportunistic pathogen
JS Brooke - Clinical microbiology reviews, 2012 - Am Soc Microbiol
Stenotrophomonas maltophilia is an emerging multidrug-resistant global opportunistic
pathogen. The increasing incidence of nosocomial and community-acquired S. maltophilia …
pathogen. The increasing incidence of nosocomial and community-acquired S. maltophilia …
Pathophysiology and management of pulmonary infections in cystic fibrosis
RL Gibson, JL Burns, BW Ramsey - American journal of respiratory …, 2003 - atsjournals.org
This comprehensive State of the Art review summarizes the current published knowledge
base regarding the pathophysiology and microbiology of pulmonary disease in cystic …
base regarding the pathophysiology and microbiology of pulmonary disease in cystic …
Nebulised hypertonic saline solution for acute bronchiolitis in infants
L Zhang, RA Mendoza-Sassi… - Cochrane database …, 2023 - cochranelibrary.com
Background Airway oedema (swelling) and mucus plugging are the principal pathological
features in infants with acute viral bronchiolitis. Nebulised hypertonic saline solution (≥ 3%) …
features in infants with acute viral bronchiolitis. Nebulised hypertonic saline solution (≥ 3%) …
A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis
MR Elkins, M Robinson, BR Rose… - … England Journal of …, 2006 - Mass Medical Soc
Background Inhaled hypertonic saline acutely increases mucociliary clearance and, in short-
term trials, improves lung function in people with cystic fibrosis. We tested the safety and …
term trials, improves lung function in people with cystic fibrosis. We tested the safety and …
Guidelines for the physiotherapy management of the adult, medical, spontaneously breathing patient
J Bott, S Blumenthal, M Buxton, S Ellum, C Falconer… - Thorax, 2009 - thorax.bmj.com
Conclusion This is the first extensive systematic literature review undertaken of the existing
evidence surrounding comprehensive physiotherapy management of the spontaneously …
evidence surrounding comprehensive physiotherapy management of the spontaneously …
Cystic fibrosis adult care: consensus conference report
JR Yankaskas, BC Marshall, B Sufian, RH Simon… - Chest, 2004 - journal.chestnet.org
Abbreviations: ADA Americans with Disabilities Act; BMD bone mineral density; BMI body
mass index; CBAVD congenital bilateral absence of the vas deferens; CF cystic fibrosis; CFF …
mass index; CBAVD congenital bilateral absence of the vas deferens; CF cystic fibrosis; CFF …
Mucus clearance and lung function in cystic fibrosis with hypertonic saline
SH Donaldson, WD Bennett, KL Zeman… - … England Journal of …, 2006 - Mass Medical Soc
Background Abnormal homeostasis of the volume of airway surface liquid in patients with
cystic fibrosis is thought to produce defects in mucus clearance and airway defense …
cystic fibrosis is thought to produce defects in mucus clearance and airway defense …
Managing cystic fibrosis: strategies that increase life expectancy and improve quality of life
M Cohen-Cymberknoh, D Shoseyov… - American journal of …, 2011 - atsjournals.org
The survival of patients with cystic fibrosis (CF) continues to improve. The discovery and
cloning of the CFTR gene more than 21 years ago led to the identification of the structure …
cloning of the CFTR gene more than 21 years ago led to the identification of the structure …
New concepts of the pathogenesis of cystic fibrosis lung disease
RC Boucher - European Respiratory Journal, 2004 - Eur Respiratory Soc
Although there has been impressive progress in the elucidation of the genetic and molecular
basis of cystic fibrosis (CF), the pathogenesis of CF lung disease remains obscure. The …
basis of cystic fibrosis (CF), the pathogenesis of CF lung disease remains obscure. The …