medline.ch Respirationstrakt Zystische Fibrose

	Association of Epithelial Alarmins and Th2 Cytokines with Disease Severity in Non-Cystic Fibrosis Bronchiectasis. Medicina (Kaunas) Gurbuz O, Baydar Toprak O, Daglioglu G, Guzel E, Mete B, Curuk B, Ozyilmaz E. PMID: 42942383 [PubMed - indexed for MEDLINE]
	Cardiovascular Manifestations of Cystic Fibrosis. J Clin Med Garg K, Agrawal A, Mustafa A, Elnashar M, Gilbert G, Rosenzveig A, Lakkimsetti A, Haroun E, Arockiam AD, Hoyek K, Tan C, Wang TKM. PMID: 42941501 [PubMed]
	Comparative plaque- and liquid-based phage susceptibility testing of Pseudomonas aeruginosa isolates in a cystic fibrosis randomized clinical trial. J Clin Microbiol Koscianski CA, Shao W, Komarow L, Parmar K, Greenwood-Quaintance KE, Souli M, Nikolich MP, Filippov AA, Schooley RT, Evans SR, Pride D, Van Tyne D, Chambers HF, Fowler VG Jr, Tamma PD, Patel R, Antibacterial Resistance Leadership Group. PMID: 42937369 [PubMed - as supplied by publisher]
	Vanzacaftor, tezacaftor and deutivacaftor fixed-dose combination for cystic fibrosis. Aust Prescr PMID: 42936244 [PubMed]
	Long-term safety and efficacy of lumacaftor/ivacaftor in children aged â‰¥12â€…months of age with cystic fibrosis: a 96-week open-label study. ERJ Open Res Zemanick ET, McColley SA, Linnemann RW, Rayment JH, Harris WT, Ramsey B, McKone EF, Tullis E, Mall MA, Taylor-Cousar JL, Sosnay PR, Ahluwalia N, Liu L, Jennings M, Rosenfeld M. PMID: 42935985 [PubMed]
	Characterizing and conceptualizing sleep in adolescents and young adults with cystic fibrosis: a descriptive qualitative study. BMC Pulm Med McMurray J, Cortinas M, Widger K, Stephenson AL, Stremler R. PMID: 42934584 [PubMed - indexed for MEDLINE]
	When cystic fibrosis is not the answer: reclassification and follow-up of children with an unresolved diagnosis after extended CFTR gene analysis. Eur J Pediatr Akca Dinç G, Tu, Bilgiç I, Kürtül Çakar M, Aktemur Ünlü A, Yeti, Y, Çavdarl, Ceylan AC, Ery, Ademhan Tural D, Cinel G. PMID: 42931970 [PubMed - indexed for MEDLINE]
	Long-term Glycemia and Risk of Death in Cystic Fibrosis-Related Diabetes: A UK Cystic Fibrosis Registry Study. Diabetes Care Adler AI, Shine B, Snowball J, Haworth C. PMID: 42930457 [PubMed - as supplied by publisher]
	Pregnancy in females with cystic fibrosis and chronic Burkholderia cepacia complex or non-tuberculous mycobacteria infection: A single centre case series. Ther Adv Respir Dis Downes A, Weitnauer L, Robinson R, Barakat S, Bowman E, Williamson C, Jones A, Simmonds NJ, Scott R, Felton I. PMID: 42929453 [PubMed - indexed for MEDLINE]
	Theratyping for personalized medicine across cystic fibrosis disease models. Commun Med (Lond) Bezzerri V, Gunawardena T, Gonska T, Chan AP, Salih R, Lucca F, Moraes TJ, Freedman SD, Cipolli M. PMID: 42928365 [PubMed]
	Impact of CFTR modulators on caregiver burden in cystic fibrosis: a cross-sectional study in Brazil. Orphanet J Rare Dis Oliveira VDGSB, Oliveira VB, Amaral MB, Miguel MD. PMID: 42920171 [PubMed - indexed for MEDLINE]
	Paediatric palliative care in advanced cystic fibrosis: from prognosis-based to needs-based care across the disease trajectory. Paediatr Respir Rev Rodrigues-Tiago B, Rolão-Carvalho C, Reis-Pina P. PMID: 42918687 [PubMed - as supplied by publisher]
	Hyperpolarized Xenon 129 MRI to Evaluate Regional Gas-Exchange Abnormalities in Cystic Fibrosis Lung Disease. Radiol Cardiothorac Imaging Soderlund SA, Masokano BI, Willmering MM, Bdaiwi AS, Hussain R, Kramer EL, Walkup LL, Cleveland ZI. PMID: 42911106 [PubMed - indexed for MEDLINE]
	Adverse events during cystic fibrosis transmembrane conductance regulator modulator therapy in children with cystic fibrosis: an observational study. Pharmacol Rep Osi, Naro, Sapiejka E, Famulska P, T, Steinert-Dymecki A, Koz, Jó, Nowakowska-Lewicka J, Bienert A, Wojsyk-Banaszak I. PMID: 42909792 [PubMed - as supplied by publisher]
	Longitudinal changes in bone mineral density among adults with cystic fibrosis: a systematic review and meta-analysis. Osteoporos Int Selvarajah A, Dittrich A, Mohandas V, Sykes J, Jad R, Strug LJ, Booth G, Batt J, Stephenson AL. PMID: 42909486 [PubMed - as supplied by publisher]
	Changes in Gastrointestinal Symptoms Among Children With Cystic Fibrosis During 12â€‰Months of Elexacaftor/Tezacaftor/Ivacaftor Therapy: A Swedish Multicentre Study. Acta Paediatr Svedberg M, Nilsson EK, Ekman P, Imberg H. PMID: 42904852 [PubMed - as supplied by publisher]
	Natural products shape microbial ecology and disease in the cystic fibrosis airway. Nat Prod Rep Bhowmik N, Stubbendieck RM. PMID: 42902746 [PubMed - as supplied by publisher]
	Bacteriophage Therapy in Cystic Fibrosis: Emerging Strategies for Managing Chronic Pseudomonas aeruginosa Infections. Drug Des Devel Ther Puthenpurayil A, Gordon L, Fothergill JL. PMID: 42898652 [PubMed - indexed for MEDLINE]
	Non-eligibility for highly effective modulator therapy with elexacaftor/tezacaftor/ivacaftor in cystic fibrosis: What about Portugal? Pulmonology Fragoso E, Azevedo P, Pereira L, Barbosa T, Cardoso AL, Cruz CM, Amorim A, Azevedo I, Almeida L, Castanhinha S, Santos AS, Gamboa F, Reis Silva T, Freitas C, Teixeira V, Carreiro A, Gonçalves J. PMID: 42898061 [PubMed - indexed for MEDLINE]
	Distinct gastrointestinal symptom phenotypes in adults with cystic fibrosis are linked to complications and medication use: the GRAMPUS-CF study. J Cyst Fibros Holaman J, Sills D, Saumtally H, Johnson C, Recto A, Marsh R, Prayle A, Gathercole K, Monaghan T, Marciani L, Spiller R, Barr HL, Downey DG, van der Gast C, Peckham D, Stewart I, Smyth A. PMID: 42888123 [PubMed - as supplied by publisher]

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