Marcus Mall to Cystic Fibrosis
This is a "connection" page, showing publications Marcus Mall has written about Cystic Fibrosis.
Connection Strength
4.019
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Multicentre standardisation of chest MRI as radiation-free outcome measure of lung disease in young children with cystic fibrosis. J Cyst Fibros. 2018 07; 17(4):518-527.
Score: 0.355
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Ion Channel Modulators in Cystic Fibrosis. Chest. 2018 08; 154(2):383-393.
Score: 0.354
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Elastase activity on sputum neutrophils correlates with severity of lung disease in cystic fibrosis. Eur Respir J. 2018 03; 51(3).
Score: 0.351
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Mucopurulent Triggering of the Airway Epithelium. Implications in Health and Cystic Fibrosis. Am J Respir Crit Care Med. 2018 02 15; 197(4):418-420.
Score: 0.348
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An informative intragenic microsatellite marker suggests the IL-1 receptor as a genetic modifier in cystic fibrosis. Eur Respir J. 2017 12; 50(6).
Score: 0.345
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Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseases. J Cyst Fibros. 2018 03; 17(2):249-255.
Score: 0.336
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MRI accelerating progress in functional assessment of cystic fibrosis lung disease. J Cyst Fibros. 2017 03; 16(2):165-167.
Score: 0.322
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Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany. Pediatr Pulmonol. 2015 Jul; 50(7):655-64.
Score: 0.287
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A new player in the game: epithelial cathepsin S in early cystic fibrosis lung disease. Am J Respir Crit Care Med. 2014 Jul 15; 190(2):126-7.
Score: 0.272
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Antisense oligonucleotide eluforsen improves CFTR function in F508del cystic fibrosis. J Cyst Fibros. 2019 07; 18(4):536-542.
Score: 0.092
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VX-659-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles. N Engl J Med. 2018 10 25; 379(17):1599-1611.
Score: 0.091
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Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis. J Cyst Fibros. 2018 11; 17(6):715-722.
Score: 0.089
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Expression and function of Anoctamin 1/TMEM16A calcium-activated chloride channels in airways of in vivo mouse models for cystic fibrosis research. Pflugers Arch. 2018 09; 470(9):1335-1348.
Score: 0.089
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Effects of Lumacaftor-Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic Fibrosis. Am J Respir Crit Care Med. 2018 06 01; 197(11):1433-1442.
Score: 0.089
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Validation of automated lobe segmentation on paired inspiratory-expiratory chest CT in 8-14 year-old children with cystic fibrosis. PLoS One. 2018; 13(4):e0194557.
Score: 0.088
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Non-contrast enhanced magnetic resonance imaging detects mosaic signal intensity in early cystic fibrosis lung disease. Eur J Radiol. 2018 Apr; 101:178-183.
Score: 0.087
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Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis. Am J Respir Crit Care Med. 2018 02 01; 197(3):410-411.
Score: 0.087
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One time quantitative PCR detection of Pseudomonas aeruginosa to discriminate intermittent from chronic infection in cystic fibrosis. J Cyst Fibros. 2018 05; 17(3):348-355.
Score: 0.087
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Bypassing CFTR dysfunction in cystic fibrosis with alternative pathways for anion transport. Curr Opin Pharmacol. 2017 06; 34:91-97.
Score: 0.085
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Chronic but not intermittent infection with Pseudomonas aeruginosa is associated with global changes of the lung microbiome in cystic fibrosis. Eur Respir J. 2017 10; 50(4).
Score: 0.085
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Hypoxia and sterile inflammation in cystic fibrosis airways: mechanisms and potential therapies. Eur Respir J. 2017 01; 49(1).
Score: 0.081