Neonates with cystic fibrosis have a reduced nasal liquid pH; A small pilot study (original) (raw)
Airway surface liquid pH is not acidic in children with cystic fibrosis
Stephen Stick
Nature communications, 2017
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Paracellular bicarbonate flux across human cystic fibrosis airway epithelia tempers changes in airway surface liquid pH
TAYYAB REHMAN
The Journal of Physiology, 2020
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Breath Condensate pH in Children With Cystic Fibrosis and AsthmaA New Noninvasive Marker of Airway Inflammation?
Dr Sergei Kharitonov MD PhD
CHEST …, 2004
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Human airway epithelial cell pH regulatory proteins in cystic fibrosis: Differential expression in nasal and bronchial airway cells
Kathleen Boyne
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Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung
Alejandro Pezzulo
Nature, 2012
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Postnatal decrease of cystic fibrosis transmembrane conductance regulator gene expression in nasal epithelium of healthy newborn infants
Cecilia Janér
Acta Paediatrica
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Inhaled Hypertonic Saline in Infants and Children Younger Than 6 Years With Cystic Fibrosis
Stephen Daniel
JAMA, 2012
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Early airway infection, inflammation, and lung function in cystic fibrosis
Claire Wainwright
Archives of Disease in Childhood, 2002
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Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children
Philippe Rosias
Pediatric Allergy and Immunology, 2008
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Breath concentration of acetic acid vapour is elevated in patients with cystic fibrosis
Patrik Spanel
Journal of breath research, 2016
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Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls
Gaudenz Hafen
Journal of Cystic Fibrosis
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Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial
Giancarlo Tancredi
Italian journal of pediatrics, 2017
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Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease
Scott Randell
Cell, 1998
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Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis
Andrew Carothers
European Respiratory Journal, 1997
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Airway ion transport impacts on disease presentation and severity in cystic fibrosis
Jean Cumps
Clinical …, 2008
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Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways
L. Clunes
Proceedings of the National Academy of Sciences, 2013
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Cystic fibrosis : clinical and laboratory studies
Sevgi Pekcan
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Relevance of Nasal Potential Difference in Diagnosis of Cystic Fibrosis Among Children
Algirdas Utkus
Medicina, 2013
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Acid exposure impairs mucus secretion and disrupts mucus transport in neonatal piglet airways
Kalina Atanasova
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Nasal and Bronchoalveolar Lavage Fluid Cytokines in Early Cystic Fibrosis
Pi-wan Cheng
Journal of Infectious Diseases, 1997
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Lung function in infants with cystic fibrosis
Ephraim Bar-yishay
Thorax, 1988
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Hypoalbuminemia at diagnosis as a marker for severe respiratory course in infants with cystic fibrosis identified by newborn screening
Keith Hammond
The Journal of Pediatrics, 1985
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Exhaled nitric oxide is not reduced in infants with cystic fibrosis
Stephen Stick
European Respiratory Journal, 2006
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Infection and Inflammation MUC up the Cystic Fibrosis Airway
Jonathan Ma
American Journal of Respiratory Cell and Molecular Biology
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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report
Michael Rock
The Journal of Pediatrics, 2008
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