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	Bridging bench and bedside: translational omics of Pseudomonas aeruginosa to validate physiologically relevant models of chronic respiratory infection in cystic fibrosis. Eur Respir Rev Wauters M, Bollé L, Van Braeckel E, Crabbé A. PMID: 42843844 [PubMed - indexed for MEDLINE]
	Residual-Function and Splicing CFTR Variants Characterize False-Negative IRT Newborn Screening: A Ten-Year Single-Center Cohort From TÃ¼rkiye. Pediatr Pulmonol Korkmaz Ç, Akp, K, Kartkaya SD, Güney AZ, Y, Öztosun B, Çollak A, Sakall. PMID: 42834588 [PubMed - indexed for MEDLINE]
	Disk diffusion and ETEST (gradient diffusion) may produce false susceptible results for Pseudomonas aeruginosa from cystic fibrosis patients due to inducible colistin tolerance. Int J Antimicrob Agents Høiby N, Wang H, Henneberg KÅ, Tolker-Nielsen T, Higazy D, Moser C, Johansen UR, Ciofu O. PMID: 42829122 [PubMed - as supplied by publisher]
	Prenatal CFTR modulator therapy for fetal cystic fibrosis: Emerging evidence, clinical considerations, and future directions. Pregnancy (Hoboken) Mustafa HJ, Blumenfeld YJ, Chmait RH, Taylor-Cousar JL, Hoppe JE, Martiniano SL, Metcalf A, Sagel SD, Zemanick ET, Shamshirsaz AA, Szentpetery SE, Trimble AT, Burgener EB, Luna-Paredes C, Sermet-Gaudelus I, Zaretsky MV. PMID: 42819752 [PubMed]
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	Delayed diagnosis of cystic fibrosis: clinical burden and missed opportunities in a cohort from Rio de Janeiro, Brazil. Respir Res Clin Pract Cohen RWF, Folescu TW, Rocha LY, Taulois M, Costa PFBM, de Oliveira RFJ. PMID: 42807610 [PubMed - indexed for MEDLINE]
	Nephrolithiasis in Cystic Fibrosis: A Gastrointestinal Perspective on Mechanisms and Management. Pediatr Pulmonol Wilder A, Schindler T, Saikumar P, Patel D, Sankararaman S. PMID: 42803148 [PubMed - indexed for MEDLINE]
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	Inhaler Devices as Potential Bacterial Reservoirs: A 30-Day Microbiota Analysis in Non-Cystic Fibrosis Bronchiectasis. Biomedicines Baek J, Sul OJ, Choi HW, Jung C, Lee S, Park J, Koo H, Kwon B, Filho FSL, Ra SW. PMID: 42792872 [PubMed]
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	The New Landscape of Cystic Fibrosis in the Era of Highly Effective Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy. J Mother Child Wo, Walicka-Serzysko K, Milczewska J, Sands D. PMID: 42790887 [PubMed - indexed for MEDLINE]
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	Contemporary 0.55 T MRI for Lung Disease Assessment in Children and Young Adults with Cystic Fibrosis: A Proof-of-Concept Study. Tomography Bayerl N, Hinsen M, Ellmann S, Nagel AM, Adams LC, Gerhalter T, Heiss R, Bäuerle T, Schmitt-Grohé S, Uder M, Rompel O, Schnell A. PMID: 42784264 [PubMed - indexed for MEDLINE]
	Early structural lung changes in young children with cystic fibrosis: a call to action. Respir Res Clin Pract Amoras ADS, Muñoz TAS, de Melo LC, Tomikawa SO, Eller MCN, Nakaie CMA, Rodrigues JC, da Silva-Filho LVRF. PMID: 42780783 [PubMed - indexed for MEDLINE]
	Maternal and fetal outcomes associated with CFTR modulator use during pregnancy: a scoping review. Eur Respir Rev Wang Z, Ruseckaite R, Dobric A, Li D, Liu Z, Wark P, Schultz A, Felton I, Bentley S, Davies J, Duckers J, Middleton PG, Taylor-Cousar JL, Richardson L, Rolnik DL, Menkhorst E, Schneider-Futschik EK. PMID: 42778208 [PubMed - indexed for MEDLINE]

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