medline.ch Respirationstrakt Zystische Fibrose

	A Question of Dose? Ultra-Low Dose Chest CT on Photon-Counting CT in People with Cystic Fibrosis. Tomography Opitz M, Welsner M, Tazeoglu HI, Stehling F, Sutharsan S, Westhölter D, Büscher E, Taube C, Guberina N, Bos D, Drews M, Rosok D, Zensen S, Haubold J, Umutlu L, Forsting M, Frings M. PMID: 41441386 [PubMed - indexed for MEDLINE]
	Impact of Elexacaftor-Tezacaftor-Ivacaftor on Muscle Composition in Cystic Fibrosis: An AI-Assisted Chest CT-Based Body Composition Analysis. Med Sci (Basel) Welsner M, Stehling F, Gruber W, Westhölter D, Sutharsan S, Taube C, Büscher E, Nensa F, Zensen S, Umutlu L, Forsting M, Haubold J, Salhöfer L, Holtkamp M, Kohnke J, Hosch R, Opitz M. PMID: 41440516 [PubMed - indexed for MEDLINE]
	Use of encapsulated dexamethasone sodium phosphate (eDSP) in chronic obstructive pulmonary disease, cystic fibrosis, and inflammatory bowel disorders. Front Drug Deliv Horn B, Mambrini G, Roden M, Schaefer C, Thye D, Magnani M. PMID: 41438155 [PubMed]
	Beyond the mutations: spatiotemporal regulation of CFTR by cAMP and calcium signaling in epithelial physiology and cystic fibrosis. Cell Mol Biol Lett Varga A, Kiss A, Crul T, Madácsy T, Pallagi P, Maléth J. PMID: 41430567 [PubMed - as supplied by publisher]
	The contemporary role of sinus surgery in managing cystic fibrosis. Curr Opin Otolaryngol Head Neck Surg Lubner RJ, Beswick DM. PMID: 41410623 [PubMed - indexed for MEDLINE]
	Comparison of n-butyl-2cyanoacrylate and tris-acryl microspheres for bronchial artery embolisation in patients with cystic fibrosis and hemoptysis: a retrospective cohort study. J Vasc Interv Radiol Ierardi AM, Ascenti V, Gramegna A, Blasi F, Del Giudice C, Xhepa G, Del Grande F, Venturini M, Carrafiello G, Coppola A. PMID: 41391833 [PubMed - as supplied by publisher]
	Correlates of FEVâ‚ deficit in pulmonary exacerbations of cystic fibrosis and associated clinical outcomes. J Cyst Fibros McElvaney OJ, Heltshe SL, Sanders DB, West NE, Fogarty B, VanDevanter DR, Flume PA, Goss CH, STOP2 Investigators. PMID: 41387145 [PubMed - as supplied by publisher]
	CYSTIC FIBROSIS NEWBORN SCREENING IN A HIGH PREVALENCE POPULATION - TEN YEARS' EXPERIENCE IN IRELAND. Respir Med McGuire F, Collins A, Elsammak M, O'Loughlin M, O'Grady L, McDaid J, Rogers M, Marsden P, Linnane B. PMID: 41386562 [PubMed - as supplied by publisher]
	Oscillation mechanics in adults with cystic fibrosis: Effect of airway obstruction and detection of early dysfunction. Respir Physiol Neurobiol Ribeiro CO, Sousa CMS, Torres MG, Oliveira RFJ, Lopes AJ, Melo PL. PMID: 41386484 [PubMed - as supplied by publisher]
	Effectiveness of the hippotherapy simulator in children and adolescents with cystic fibrosis: A randomized controlled trial. Heart Lung Cinar B, Demir R, Zeren M, Cakir E, Gurses HN. PMID: 41385838 [PubMed - as supplied by publisher]
	Diagnostic and prognostic value of miR-155 in non-cystic fibrosis bronchiectasis. BMC Pulm Med Li W, Yu X, Wang W, Liang R, Luo Z, Zou X, Lin L, Zhang K, Wu Y. PMID: 41382178 [PubMed - as supplied by publisher]
	Comparative efficacy and safety of CFTR modulators for people with cystic fibrosis with phe508del mutation: a systematic review and bayesian network meta-analysis. EClinicalMedicine Safeer V S M, Behl S, Vaidya PC, Tiwari P, Bharti SK, Nahan N, Kumar Sahu J, Bansal D. PMID: 41377908 [PubMed]
	Methodological Assessment of High-Throughput Sequencing Platforms: Illumina vs. MGI in Clinical-Grade CFTR Genotyping. Int J Mol Sci Beggio M, Peroni E, Greco E, Favretto G, Degiorgio D, Rosato A, Favarato M. PMID: 41373845 [PubMed - indexed for MEDLINE]
	Role of the ADAM33 rs2280091 Variant in Modulating Lung Function in Cystic Fibrosis. Int J Mol Sci Dos Santos VS, Mello LS, Marques LFA, Silva LR, Bertuzzo CS, Ribeiro JD, Marson FAL. PMID: 41373738 [PubMed - indexed for MEDLINE]
	Transforming Care Models in Cystic Fibrosis: A Review. Healthcare (Basel) Diener BL, Berdella M, DeCelie-Germana J, Stables-Carney T, Kier C. PMID: 41373238 [PubMed]
	Digital technology for monitoring adherence to inhaled therapies in people with cystic fibrosis. Cochrane Database Syst Rev Calthorpe R, Smith S, Jahnke N, Smyth AR, supported by the Cochrane Cystic Fibrosis Review Group. PMID: 41368989 [PubMed - indexed for MEDLINE]
	Elexacaftor/tezacaftor/ivacaftor corrects salt-wasting in cystic fibrosis. J Cyst Fibros Berg P, Rousing AQ, Jensen-Fangel S, Bandulik S, Warth R, Sørensen MV, Jeppesen M, Leipziger J. PMID: 41365775 [PubMed - as supplied by publisher]
	Transitioning care in cystic fibrosis: a comprehensive review of reviews of clinical and psychosocial outcomes. Front Pediatr Alzayed A. PMID: 41357806 [PubMed]
	Heterogeneous use of multiple breath washout in cystic fibrosis across age groups and European countries: an ECFSPR analysis. J Cyst Fibros Zolin A, Gambazza S, Lindblad A, Gkolia P, Saunders C, Naehrlich L, European Cystic Fibrosis Society Patient Registry Steering Group. PMID: 41354586 [PubMed - as supplied by publisher]
	DNA methylation predicts lung function and pulmonary exacerbation in sputum samples from patients with cystic fibrosis. Clin Epigenetics Tost J, Caimmi D, Pastore M, Reynes C, Busato F, Pineau F, Claustres M, Vachier I, Chiron R, De Sario A. PMID: 41351062 [PubMed - as supplied by publisher]

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