medline.ch Respirationstrakt Zystische Fibrose

	Unmet challenges in cystic fibrosis treatment with modulators. Expert Rev Respir Med Corrao F, Kelly-Aubert M, Sermet-Gaudelus I, Semeraro M. PMID: 38755109 [PubMed - as supplied by publisher]
	The intertwining of discourses in the diagnostic construction of cystic fibrosis: a perspective on access and barriers. Cien Saude Colet Marins KAC, Moreira MCN. PMID: 38747779 [PubMed - indexed for MEDLINE]
	Distribution of pathogenic variants in the CFTR gene in a representative cohort of people with cystic fibrosis in the Kingdom of Bahrain. Mol Genet Genomics Majed OAK, Majed FO, Almoamen NJ, Alsatrawi HB, Shehabi SD, Hrbková J, Libik M, Macek M Jr. PMID: 38744777 [PubMed - indexed for MEDLINE]
	[Italian Cystic Fibrosis Registry (ICFR). Report 2021-2022]. Epidemiol Prev Campagna G, Amato A, Majo F, Ferrari G, Quattrucci S, Padoan R, Floridia G, Salvatore D, Carnovale V, Puppo Fornaro G, Taruscio D, Salvatore M, Gruppo di lavoro RIFC. PMID: 38742380 [PubMed - indexed for MEDLINE]
	Exploring the dynamics of mixed-species biofilms involving Candida spp. and bacteria in cystic fibrosis. Arch Microbiol Gourari-Bouzouina K, Boucherit-Otmani Z, Halla N, Seghir A, Baba Ahmed-Kazi Tani ZZ, Boucherit K. PMID: 38734793 [PubMed - indexed for MEDLINE]
	Insights and considerations on CFTR variant reporting in a study of cystic fibrosis patients in Saudi Arabia CFTR 1548del G and 1549del G: Navigating the discovery of novel mutations. Saudi Med J Al Abdulsalam EA. PMID: 38734430 [PubMed - indexed for MEDLINE]
	Vitamin K Status Based on K1, MK-4, MK-7, and Undercarboxylated Prothrombin Levels in Adolescent and Adult Patients with Cystic Fibrosis: A Cross-Sectional Study. Nutrients Krzy, Nowak J, Kara, Jamka M, Klapkova E, Kurek S, Drzyma, Lisowska A, Wojsyk-Banaszak I, Skorupa W, Szyd, Prusa R, Walkowiak J. PMID: 38732584 [PubMed - indexed for MEDLINE]
	Identifying people living with cystic fibrosis in the Danish National Patient Registry: A validation study. J Cyst Fibros Råket HK, Wang JN, Petersen J, Pressler T, Olesen HV, Jensen-Fangel S, Bryrup T, Jimenez-Solem E, Jensen CB. PMID: 38729850 [PubMed - as supplied by publisher]
	Musculoskeletal aspects of respiratory function in cystic fibrosis: a cross-sectional comparative study. Eur Clin Respir J Sinderholm Sposato N, Bjerså K, Gilljam M, Lannefors L, Fagevik Olsén M. PMID: 38726022 [PubMed]
	A model for oversight of rare disease studies: The 25-year experience of the cystic fibrosis foundation data safety monitoring board. J Cyst Fibros Quittell LM, Simon RH, Morgan W. PMID: 38719765 [PubMed - as supplied by publisher]
	[Cystic fibrosis in childhood and adulthood]. Inn Med (Heidelb) Syunyaeva Z, Mall MA, Stahl M. PMID: 38714556 [PubMed - as supplied by publisher]
	Clinical and anthropometric evolution of individuals with cystic fibrosis during COVID-19 pandemic: A 24-month cohort study. Pediatr Pulmonol de Oliveira TJ, Altoé ID, Arpini LDSB, Liberato FMG, Melotti RCNC, Wittmer VL, Duarte H, Barbalho-Moulim MC, Paro FM. PMID: 38712790 [PubMed - as supplied by publisher]
	In vitro activity of cefiderocol in Pseudomonas aeruginosa isolates from people with cystic fibrosis recovered during three multicentre studies in Spain. J Antimicrob Chemother Maruri-Aransolo A, López-Causapé C, Hernández-García M, García-Castillo M, Caballero-Pérez JD, Oliver A, Cantón R. PMID: 38708553 [PubMed - as supplied by publisher]
	Metabolic complications in lung transplantation for cystic fibrosis - A case control study. Heliyon Lam GY, Patel H, Sharpe H, Li D, Halloran K. PMID: 38707432 [PubMed]
	Widespread alterations in systemic immune profile are linked to lung function heterogeneity and airway microbes in cystic fibrosis. J Cyst Fibros Rossi E, Lausen M, Øbro NF, Colque A, Nielsen BU, Møller R, de Gier C, Hald A, Skov M, Pressler T, Molin S, Ostrowski SR, Marquart HV, Johansen HK. PMID: 38702223 [PubMed - as supplied by publisher]
	Considerations for the use of inhaled antibiotics for Pseudomonas aeruginosa in people with cystic fibrosis receiving CFTR modulator therapy. BMJ Open Respir Res Burgel PR, Ballmann M, Drevinek P, Heijerman H, Jung A, Mainz JG, Peckham D, Plant BJ, Schwarz C, Taccetti G, Smyth A. PMID: 38702073 [PubMed - indexed for MEDLINE]
	Bronchoscopy-guided antimicrobial therapy for cystic fibrosis. Cochrane Database Syst Rev Jain K, Wainwright CE, Smyth AR. PMID: 38700027 [PubMed - indexed for MEDLINE]
	CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways. Front Physiol Wu M, Chen JH. PMID: 38699141 [PubMed]
	A randomized trial of oral prednisone for cystic fibrosis pulmonary exacerbation treatment. Eur Respir J Waters V, Shaw M, Perrem L, Quon BS, Tullis E, Solomon M, Rayment JH, Lavoie A, Tse SM, Daigneault P, Bilodeau L, Price A, Nicholson M, Chin M, Parkins M, McKinney ML, Tam JS, Stanojevic S, Grasemann H, Ratjen F, PIPE Study Investigators. PMID: 38697648 [PubMed - as supplied by publisher]
	Cutaneous Manifestations of Cystic Fibrosis. J Am Acad Dermatol Smith AD, Schwartzman G, Lyons CE, Flowers H, Albon D, Greer K, Lonabaugh K, Zlotoff BJ. PMID: 38697219 [PubMed - as supplied by publisher]

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