medline.ch Respirationstrakt Zystische Fibrose

	SERS Microsensors for the Study of pH Regulation in Cystic Fibrosis Patient-Derived Airway Cultures. ACS Sens Skinner WH, Robinson N, Hardisty GR, Gray RD, Campbell CJ. PMID: 38659220 [PubMed - as supplied by publisher]
	Exploring the link between a novel approach for computer aided lung sound analysis and imaging biomarkers: a cross-sectional study. Respir Res Lauwers E, Stas T, McLane I, Snoeckx A, Van Hoorenbeeck K, De Backer W, Ides K, Steckel J, Verhulst S. PMID: 38658980 [PubMed - indexed for MEDLINE]
	Elexacaftor/tezacaftor/ivacaftor influences body composition in adults with cystic fibrosis: a fully automated CT-based analysis. Sci Rep Westhölter D, Haubold J, Welsner M, Salhöfer L, Wienker J, Sutharsan S, Straßburg S, Taube C, Umutlu L, Schaarschmidt BM, Koitka S, Zensen S, Forsting M, Nensa F, Hosch R, Opitz M. PMID: 38658613 [PubMed - indexed for MEDLINE]
	Cystic fibrosis newborn screening in Switzerland - evaluation and scenarios for improvement after 11 years of follow-up. J Cyst Fibros Pedersen E, de Jong Carmen CM, Jurca M, Berger DO, Sanz J, Sluka S, Poms M, Baumgartner MR, Regamey N, Kuehni CE, Barben J, Rueegg CS, Swiss Cystic Fibrosis Newborn Screening Group. PMID: 38658252 [PubMed - as supplied by publisher]
	Attitudes to cross infection, nebuliser hygiene and antimicrobial resistance in people with cystic fibrosis: Results of an international survey. Infect Dis Health Millar BC, Rendall JC, Moore JE. PMID: 38644104 [PubMed - as supplied by publisher]
	Short-term azithromycin use is associated with QTc interval prolongation in children with cystic fibrosis. Arch Pediatr Enho, Do, Yozgat CY, Cak, Yazan H, Erol AB, Erenberk U, Yozgat Y. PMID: 38637249 [PubMed - as supplied by publisher]
	Bronchiectasis not due to cystic fibrosis. Med Clin (Barc) Girón R, Golpe R, Martínez-García MÁ. PMID: 38637217 [PubMed - as supplied by publisher]
	Pathophysiology of non-cystic fibrosis bronchiectasis in children and adolescents with asthma: A protocol for systematic review and meta-analysis. PLoS One da Silva NC, Malagutti BC, Ladeira JMCD, Grotta MB, Toro AADC. PMID: 38635522 [PubMed - indexed for MEDLINE]
	Recommended Tool Compounds for Modifying the Cystic Fibrosis Transmembrane Conductance Regulator Channel Variants. ACS Pharmacol Transl Sci Han X, Li D, Zhu Y, Schneider-Futschik EK. PMID: 38633590 [PubMed]
	The role of volatile organic compounds for assessing characteristics and severity of non-cystic fibrosis bronchiectasis: an observational study. Front Med (Lausanne) Gu SY, Lu HW, Bai JW, Yang JW, Mao B, Yu L, Xu JF. PMID: 38633315 [PubMed]
	A new era of targeting cystic fibrosis with non-viral delivery of genomic medicines. Adv Drug Deliv Rev Turuvekere Vittala Murthy N, Vlasova K, Renner J, Jozic A, Sahay G. PMID: 38626860 [PubMed - as supplied by publisher]
	The effect of respiratory muscle training on children and adolescents with cystic fibrosis: a systematic review and meta-analysis. BMC Pediatr Cai W, Li M, Xu Y, Li M, Wang J, Zuo Y, Cao J. PMID: 38622583 [PubMed - indexed for MEDLINE]
	Safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with Cystic Fibrosis following liver transplantation: A systematic review. J Cyst Fibros Testa I, Indolfi G, Brugha R, Verkade HJ, Terlizzi V. PMID: 38614868 [PubMed - as supplied by publisher]
	Impact of 1-Year Supplementation with High-Rich Docosahexaenoic Acid (DHA) on Clinical Variables and Inflammatory Biomarkers in Pediatric Cystic Fibrosis: A Randomized Double-Blind Controlled Trial. Nutrients Ayats-Vidal R, Bosque-García M, Cordobilla B, Asensio-De la Cruz O, García-González M, Loureda-Pérez S, Fernández-López E, Robert-Barriocanal E, Valiente-Planas A, Domingo JC. PMID: 38613004 [PubMed - indexed for MEDLINE]
	Beyond Borders of the Cell: How Extracellular Vesicles Shape COVID-19 for People with Cystic Fibrosis. Int J Mol Sci Hejenkowska ED, Yavuz H, Swiatecka-Urban A. PMID: 38612524 [PubMed - indexed for MEDLINE]
	Diagnosing Cystic Fibrosis in the 21st Century-A Complex and Challenging Task. Diagnostics (Basel) Anton-P, Azoic, Trofin F, Mîndru DE, Murgu AM, Bocec AS, Iliescu Hali, Ciongradi CI, S, Iliescu ML. PMID: 38611676 [PubMed]
	The prevalence of developmental defects of enamel in people with cystic fibrosis: a systematic review. BMC Oral Health O'Leary F, Coffey N, Hayes M, Burke F, Harding M, Plant B. PMID: 38609911 [PubMed - indexed for MEDLINE]
	Azithromycin reduces bronchial wall thickening in infants with cystic fibrosis. J Cyst Fibros Chen Y, Charbonnier JP, Andrinopoulou ER, Sly PD, Stick SM, Tiddens HAWM, COMBAT-CF Study Group. PMID: 38584038 [PubMed - as supplied by publisher]
	Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID. Pediatrics Green DM, Lahiri T, Raraigh KS, Ruiz F, Spano J, Antos N, Bonitz L, Christon L, Gregoire-Bottex M, Hale JE, Langfelder-Schwind E, La Parra Perez Á, Maguiness K, Massie J, McElroy-Barker E, McGarry ME, Mercier A, Munck A, Oliver KE, Self S, Singh K, Smiley M, Snodgrass S, Tluczek A, Tuley P, Lomas P, Wong E, Hempstead SE, Faro A, Ren CL. PMID: 38577740 [PubMed - as supplied by publisher]
	Adapting, restarting, and terminating a randomised control trial for people with cystic fibrosis: Reflections on the impact of the COVID-19 pandemic upon research in a clinical population. Contemp Clin Trials Commun Tomlinson OW, Barker AR, Denford S, Williams CA. PMID: 38577655 [PubMed]

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