The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis Airway von Mirković, Bojana, Murray, Michelle A, Lavelle, Gillian M, Molloy, Kevin, Azim, Ahmed Abdul, Gunaratnam, Cedric, Healy, Fiona, Slattery, Dubhfeasa, McNally, Paul, Hatch, Joe, Wolfgang, Matthew, Tunney, Michael M, Muhlebach, Marianne S, Devery, Rosaleen, Greene, Catherine M, McElvaney, Noel G

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The microbial community of the cystic fibrosis airway is disrupted in early life von Renwick, Julie, McNally, Paul, John, Bettina, DeSantis, Todd, Linnane, Barry, Murphy, Philip

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A multimodal iPSC platform for cystic fibrosis drug testing von Berical, Andrew, Lee, Rhianna E., Lu, Junjie, Beermann, Mary Lou, Le Suer, Jake A., Mithal, Aditya, Thomas, Dylan, Ranallo, Nicole, Peasley, Megan, Stuffer, Alex, Bukis, Katherine, Seymour, Rebecca, Harrington, Jan, Coote, Kevin, Valley, Hillary, Hurley, Killian, McNally, Paul, Mostoslavsky, Gustavo, Mahoney, John, Randell, Scott H., Hawkins, Finn J.

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The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6-11 with cystic fibrosis in a real-world setting von McNally, Paul, Linnane, Barry, Williamson, Michael, Elnazir, Basil, Short, Christopher, Saunders, Clare, Kirwan, Laura, David, Rea, Kemner-Van de Corput, Mariette P C, Tiddens, Harm A W M, Davies, Jane C, Cox, Des W

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Lipoxin A4 stimulates calcium-activated chloride currents and increases airway surface liquid height in normal and cystic fibrosis airway epithelia von Verrière, Valia, Higgins, Gerard, Al-Alawi, Mazen, Costello, Richard W, McNally, Paul, Chiron, Raphaël, Harvey, Brian J, Urbach, Valérie

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Rapid repair of percutaneous endoscopic gastrostomy tubes using three-dimensional printing: A case series von O'Sullivan, Kevin J., O'Sullivan, Aidan G., Kermavnar, Tjaša, McNally, Paul, Dunne, Colum P., Linnane, Barry, O'Sullivan, Leonard W.

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Elafin, an Elastase-specific Inhibitor, Is Cleaved by Its Cognate Enzyme Neutrophil Elastase in Sputum from Individuals with Cystic Fibrosis von Guyot, Nicolas, Butler, Marcus W., McNally, Paul, Weldon, Sinead, Greene, Catherine M., Levine, Rodney L., O'Neill, Shane J., Taggart, Clifford C., McElvaney, Noel G.

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A role for whey acidic protein four-disulfide-core 12 (WFDC12) in the regulation of the inflammatory response in the lung von Glasgow, Arlene M A, Small, Donna M, Scott, Aaron, McLean, Denise T, Camper, Nicolas, Hamid, Umar, Hegarty, Shauna, Parekh, Dhruv, O'Kane, Cecilia, Lundy, Fionnuala T, McNally, Paul, Elborn, J Stuart, McAuley, Danny F, Weldon, Sinéad, Taggart, Clifford C

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Dysregulation of TIM-3-galectin-9 pathway in the cystic fibrosis airways von Vega-Carrascal, Isabel, Reeves, Emer P, Niki, Toshiro, Arikawa, Tomohiro, McNally, Paul, O'Neill, Shane J, Hirashima, Mitsuomi, McElvaney, Noel G

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Appearance of Pancreatic Sufficiency and Discontinuation of Pancreatic Enzyme Replacement Therapy in Children with Cystic Fibrosis on Ivacaftor von Hutchinson, Ingrid, McNally, Paul

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Six-lobe bronchoalveolar lavage in children with cystic fibrosis von Linnane, Barry, McNally, Paul

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A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/lvacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele von Zemanick, Edith T., Taylor-Cousar, Jennifer L., Davies, Jane, Gibson, Ronald L., Mall, Marcus A., McKone, Edward F., McNally, Paul, Ramsey, Bonnie W., Rayment, Jonathan H., Rowe, Steven M., Tullis, Elizabeth, Ahluwalia, Neil, Chu, Chenghao, Ho, Thang, Moskowitz, Samuel M., Noel, Sabrina, Tian, Simon, Waltz, David, Weinstock, Tanya G., Xuan, Fengjuan, Wainwright, Claire E., McColley, Susanna A.

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Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertension von McGovern, Eiméar, McNally, Paul, O’Sullivan, Maureen, Phelan, Ethna, Sumner, Kelli, Best, D. Hunter, McMahon, Colin J.

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Performance Characteristics, Intra‐ and Inter‐Operator Agreement of Transient Elastography in Pediatric Nonalcoholic Fatty Liver Disease von Rowland, Marion, McGee, Allison, McNally, Paul, Bourke, Billy

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Lower Airway Infection in Preschool Children with Cystic Fibrosis: An International Comparison von Hulme, Kathryn M., Linnane, Barry, McNally, Paul

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Performance Characteristics, Intra- and Inter-Operator Agreement of Tramnsient Elastography in Pediatric Nonalcoholic Fatty Liver Disease von Rowland, Marion, McGee, Allison, McNally, Paul, Bourke, Billy

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A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele von Zemanick, Edith T, Taylor-Cousar, Jennifer L, Davies, Jane, Gibson, Ronald L, Mall, Marcus A, McKone, Edward F, McNally, Paul, Ramsey, Bonnie W, Rayment, Jonathan H, Rowe, Steven M, Tullis, Elizabeth, Ahluwalia, Neil, Chu, Chenghao, Ho, Thang, Moskowitz, Samuel M, Noel, Sabrina, Tian, Simon, Waltz, David, Weinstock, Tanya G, Xuan, Fengjuan, Wainwright, Claire E, McColley, Susanna A

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Chronic rhinosinusitis in the era of CFTR modulator therapy von Stone, Roy Gavin, Short, Christopher, Davies, Jane C, McNally, Paul

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Silence of the lungs: comparing measures of slow and noncommunicating lung units from pulmonary function tests with computed tomography von Short, Christopher, Semple, Thomas, Abkir, Mary, Padley, Simon, Rosenthal, Mark, McNally, Paul, Tiddens, Harm, Caudri, Daan, Bush, Andrew, Davies, Jane C

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Improvement in Lung Clearance Index and Chest Computed Tomography Scores with Elexacaftor/Tezacaftor/Ivacaftor Treatment in People with Cystic Fibrosis Aged 12 Years and Older - Th... von McNally, Paul, Lester, Karen, Stone, Gavin, Elnazir, Basil, Williamson, Michael, Cox, Des, Linnane, Barry, Kirwan, Laura, Rea, David, O'Regan, Paul, Semple, Tom, Saunders, Clare, Tiddens, Harm A W M, McKone, Edward, Davies, Jane C

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