medline.ch Respirationstrakt Zystische Fibrose

	CFTR Functional Rescue and Heterogeneous Clinical Outcomes Following Elexacaftor/Tezacaftor/Ivacaftor Therapy in People with Cystic Fibrosis Carrying the W1282R Variant. Int J Mol Sci Kondratyeva E, Efremova A, Melyanovskaya Y, Zhekaite E, Sapelnikova M, Milovanov M, Shchagina O, Voronkova A, Sherman V, Krasovsky S, Kutsev S, Goldshtein D. PMID: 42884140 [PubMed - indexed for MEDLINE]
	Beyond Tuberculosis: Late Diagnosis of Cystic Fibrosis in an Adolescent with Bronchiectasis and Recurrent Pseudomonas aeruginosa Isolation: A Case Report. Diagnostics (Basel) Mihailov OM, Lu, , Mihailov R, Stav, . PMID: 42882257 [PubMed]
	Late-Diagnosed Cystic Fibrosis with Co-Occurring CFTR 3849+10kbC>T and 5T Variants: A Case Report. J Clin Med Popovici P, Mihai A, Butnariu LI, Popovici RM, Murgu AM, Tarc, Ioniuc IK, Rusu TE, Anton-P, Temneanu OR. PMID: 42882046 [PubMed]
	Model-informed dose reduction of elexacaftor/tezacaftor/ivacaftor therapy in adult people with cystic fibrosis: A simulation study. J Cyst Fibros Zwart TC, Baromeo SB, Bronsveld I, Heijerman HG, Wilms EB, van der Meer R. PMID: 42881074 [PubMed - as supplied by publisher]
	The impact of modulator therapy on the Pseudomonas aeruginosa cystic fibrosis lung transcriptome. Proc Natl Acad Sci U S A Letizia M, Whiteley LE, Diggle FL, Davis AN, Morgan SJ, Grogan B, Baugh J, McKone EF, Singh PK, Whiteley M. PMID: 42879475 [PubMed - indexed for MEDLINE]
	Assessment of Cystic Fibrosis Lung Disease Using Electrical Impedance Tomography. Pediatr Pulmonol Boas H, Bennett L, Faerber J, Donnelly EC, Gari M, Sailman GE, Pierdomenico A, Napolitano N, Dorgan D, Panitch HB, Ren CL. PMID: 42878537 [PubMed - indexed for MEDLINE]
	Fractional exhaled nitric oxide in non-cystic fibrosis bronchiectasis: an exploratory prospective observational study. Monaldi Arch Chest Dis Dilka E, Duraku E, Simaku A, Kapisyzi P. PMID: 42876314 [PubMed - as supplied by publisher]
	[Cystic Fibrosis in Latin America: Clinical Practices, Diagnosis, and Therapeutic Access: a Multicenter Cross-sectional Study]. Acta Gastroenterol Latinoam Higuera Carrillo M, Arregui MC, Arcucci MS, Reyes-Apodaca M, Navarro Díaz E, Sereno V, Oropeza Gianfelici G, Rodríguez Guerrero M, Jijón Andrade MC, Alomía M, Boldrini G, González Rozó N, Previte Nastasi P, Ortiz Paranza L. PMID: 42872225 [PubMed]
	Navigating School While Living With Cystic Fibrosis: Barriers and Support Strategies From the Patient and Family Perspective. Pediatr Pulmonol Heimbruch K, Strong S, Wackler M, Taylor M, Duan Q, Filigno SS, Hjelm M. PMID: 42870664 [PubMed - indexed for MEDLINE]
	How cystic fibrosis modulator therapy could transform Pseudomonas aeruginosa epidemiology. Microbiology (Reading) Gurney J, Letizia M, Azimi S, Diggle SP. PMID: 42867880 [PubMed - indexed for MEDLINE]
	Treatment adherence and mental health in people with cystic fibrosis and advanced lung disease treated with elexacaftor/tezacaftor/ivacaftor. Pulmonology Terlizzi V, Graziano S, Presti S, Malanima MA, Fevola C, Castaldo A, Teodori C, Bresci S, Avarello A, Quittner AL, Lucenteforte E. PMID: 42861492 [PubMed - indexed for MEDLINE]
	Comfort discussing financial challenges and accessing resources in cystic fibrosis care among people with cystic fibrosis and their care partners: A cross-sectional survey study. J Cyst Fibros Perkins RC, Carey K, King JR, Beidler L, Moo-Young J, Broekema K, Sawicki GS, Benitez D, Brown AW, Duncan C, Groenendyk I, McGarry ME, Phan H, Ren CL, Shaver A, Willis A, Dieni O, Van Citters AD. PMID: 42859077 [PubMed - as supplied by publisher]
	Value-based pricing of brensocatib for frequently exacerbating non-cystic fibrosis bronchiectasis in China: a China-adapted, FEV(1)-inclusive time-dependent markov analysis. Front Pharmacol Zhang D, Hu P, Zhang W, Zhang W. PMID: 42856781 [PubMed]
	Handheld lung ultrasound for assessing cystic fibrosis lung disease in children: a diaphragm-Ä±ntegrated scoring approach. Eur J Pediatr Akyan Soyda, Özkan Tabakç, Bilgiç I, Kürtül Çakar M, Akça Dinç G, Aktemur Ünlü A, Tokdemir BE, Yeti, Y, Dil, Ademhan Tural D, Ery, Keçeli AM, Cinel G. PMID: 42853414 [PubMed - indexed for MEDLINE]
	From an emerging pathogen to therapeutic challenges: advances in Achromobacter species, with a focus on A. xylosoxidans and cystic fibrosis. Front Microbiol Xiang Y, Xiong D, Liu X. PMID: 42851702 [PubMed]
	Timeliness to diagnostic and early care milestones after newborn screening for Cystic Fibrosis in Texas: 14 years of experience at 2 centers. J Cyst Fibros Pottorff A, Knight S, Cannon CL, Lee M, Ren CL, Ruiz F, Tuley P, Willey-Courand DB, Wong C, Sathe M. PMID: 42850178 [PubMed - as supplied by publisher]
	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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