Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline von Shapiro, Adam J, Davis, Stephanie D, Polineni, Deepika, Manion, Michele, Rosenfeld, Margaret, Dell, Sharon D, Chilvers, Mark A, Ferkol, Thomas W, Zariwala, Maimoona A, Sagel, Scott D, Josephson, Maureen, Morgan, Lucy, Yilmaz, Ozge, Olivier, Kenneth N, Milla, Carlos, Pittman, Jessica E, Daniels, M Leigh Anne, Jones, Marcus Herbert, Janahi, Ibrahim A, Ware, Stephanie M, Daniel, Sam J, Cooper, Matthew L, Nogee, Lawrence M, Anton, Billy, Eastvold, Tori, Ehrne, Lynn, Guadagno, Elena, Knowles, Michael R, Leigh, Margaret W, Lavergne, Valery

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Ciliary functional analysis: Beating a path towards standardization von Kempeneers, Céline, Seaton, Claire, Garcia Espinosa, Bernardo, Chilvers, Mark A.

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Inconclusive diagnosis of cystic fibrosis after newborn screening von Ooi, Chee Y, Castellani, Carlo, Keenan, Katherine, Avolio, Julie, Volpi, Sonia, Boland, Margaret, Kovesi, Tom, Bjornson, Candice, Chilvers, Mark A, Morgan, Lenna, van Wylick, Richard, Kent, Steven, Price, April, Solomon, Melinda, Tam, Karen, Taylor, Louise, Malitt, Kylie-Ann, Ratjen, Felix, Durie, Peter R, Gonska, Tanja

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Variation of Ciliary Beat Pattern in Three Different Beating Planes in Healthy Subjects von Kempeneers, Celine, MD, Seaton, Claire, BM BCh, Chilvers, Mark A., MD

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Peroxisome deficiency underlies failures in hepatic immune cell development and antigen presentation in a severe Zellweger disease model von Parsons, Brendon D., Medina-Luna, Daniel, Scur, Michal, Pinelli, Marinella, Gamage, Gayani S., Chilvers, Rebecca A., Hamon, Yannick, Ahmed, Ibrahim H.I., Savary, Stéphane, Makrigiannis, Andrew P., Braverman, Nancy E., Rodriguez-Alcazar, Juan F., Latz, Eicke, Karakach, Tobias K., Di Cara, Francesca

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Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia von Chilvers, Mark A, Rutman, Andrew, O'Callaghan, Christopher

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Inflammasome-mediated IL-1β production in humans with cystic fibrosis von Tang, Anthony, Sharma, Ashish, Jen, Roger, Hirschfeld, Aaron F, Chilvers, Mark A, Lavoie, Pascal M, Turvey, Stuart E

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Functional analysis of cilia and ciliated epithelial ultrastructure in healthy children and young adults von Chilvers, M A, Rutman, A, O'Callaghan, C

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Analysis of ciliary beat pattern and beat frequency using digital high speed imaging: comparison with the photomultiplier and photodiode methods von Chilvers, Mark A, O'Callaghan, Christopher

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Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis von Ooi, Chee Y, Sutherland, Rosie, Castellani, Carlo, Keenan, Katherine, Boland, Margaret, Reisman, Joe, Bjornson, Candice, Chilvers, Mark A, van Wylick, Richard, Kent, Steven, Price, April, Mateos-Corral, Dimas, Hughes, Daniel, Solomon, Melinda, Zuberbuhler, Peter, Brusky, Janna, Durie, Peter R, Ratjen, Felix, Gonska, Tanja

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Atypical activation of the unfolded protein response in cystic fibrosis airway cells contributes to p38 MAPK-mediated innate immune responses von Blohmke, Christoph J, Mayer, Matthew L, Tang, Anthony C, Hirschfeld, Aaron F, Fjell, Christopher D, Sze, Marc A, Falsafi, Reza, Wang, Shirley, Hsu, Karolynn, Chilvers, Mark A, Hogg, James C, Hancock, Robert E W, Turvey, Stuart E

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To beat, or not to beat, that is question! The spectrum of ciliopathies von Kempeneers, Céline, Chilvers, Mark A.

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Lung Cancer and Interstitial Lung Diseases: A Systematic Review von Archontogeorgis, Kostas, Steiropoulos, Paschalis, Tzouvelekis, Argyris, Nena, Evangelia, Bouros, Demosthenes

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Remaking Participation: Science, environment and emergent publics von Chilvers, Jason, Kearnes, Matthew

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Efficacy and Safety of Ivacaftor in Patients Aged 6 to 11 Years with Cystic Fibrosis with a G551D Mutation von DAVIES, Jane C, WAINWRIGHT, Claire E, ORDONEZ, Claudia L, AHRENS, Richard, CANNY, Gerard J, CHILVERS, Mark A, HOWENSTINE, Michelle S, MUNCK, Anne, MAINZ, Jochen G, RODRIGUEZ, Sally, HAIHONG LI, YEN, Karl

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Long-term safety and efficacy of lumacaftor–ivacaftor therapy in children aged 6–11 years with cystic fibrosis homozygous for the F508del-CFTR mutation: a phase 3, open-label, exte... von Chilvers, Mark A, Davies, Jane C, Milla, Carlos, Tian, Simon, Han, Zifei, Cornell, Alexandra G, Owen, Caroline A, Ratjen, Felix

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Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age von Gonska, Tanja, Keenan, Katherine, Au, Jacky, Dupuis, Annie, Chilvers, Mark A., Burgess, Caroline, Bjornson, Candice, Fairservice, Lori, Brusky, Janna, Kherani, Tamizan, Jober, Amanda, Kosteniuk, Lorna, Price, April, Itterman, Jennifer, Morgan, Lenna, Mateos-Corral, Dimas, Hughes, Daniel, Donnelly, Christine, Smith, Mary Jane, Iqbal, Shaikh, Arpin, Jocelyn, Reisman, Joe, Hammel, Joanne, van Wylick, Richard, Derynck, Michael, Henderson, Natalie, Solomon, Melinda, Ratjen, Felix

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The effects of coronavirus on human nasal ciliated respiratory epithelium von Chilvers, M.A, McKean, M, Rutman, A, Myint, B.S, Silverman, M, O'Callaghan, C

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An investigation into biomarkers for the diagnosis of ABPA and aspergillus disease in cystic fibrosis von Keown, Karen, Abbott, Salome, Kuzeljevic, Boris, Rayment, Jonathan H., Chilvers, Mark A., Yang, Connie L.

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Long‐term respiratory outcomes following solid organ transplantation in children: A retrospective cohort study von Wright, M. F. A., Blydt‐Hansen, T., Chilvers, M. A.

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