medline.ch Respirationstrakt Zystische Fibrose

	Cystic Fibrosis of the Pancreas: In Vitro Duct Models for CFTR-Targeted Translational Research. Int J Mol Sci Ludovico A, Battistini M, Baroni D. PMID: 41683706 [PubMed - indexed for MEDLINE]
	Psychosocial Aspects of Cystic Fibrosis: A Mixed-Methods Systematic Review. Healthcare (Basel) Griff MI, Santos R, Trumello C, Brandão T. PMID: 41682201 [PubMed]
	Sleep-Disordered Breathing in Cystic Fibrosis in Low- and Middle-Income Countries. Pediatr Pulmonol Balc, Gökdemir Y, Eralp EE, Ersu R. PMID: 41677092 [PubMed - indexed for MEDLINE]
	The CARMUCI Study Design: A Double-Blind, Cross-Over Sham-Controlled Trial of Indoor Air Purification in People With Cystic Fibrosis and Primary Ciliary Dyskinesia. Pediatr Pulmonol Kakkoura MG, Anagnostopoulou P, Kouis P, Michanikou A, Bargiotas P, Adamides T, Ioannou P, Louka SF, Neophytou M, Nikolopoulos GK, Skevaki C, Koutrakis P, Yiallouros PK. PMID: 41674312 [PubMed - indexed for MEDLINE]
	Hypertonic saline in non-cystic fibrosis bronchiectasis (Hyper-BRONCHI): an updated systematic review and meta-analysis. BMC Pulm Med Nguyen N, Zawam Y, Tran NB, de Barros E Lyra NA, Ho VQT, Downes D, Nguyen VND, Le HDT, Aljazeeri J. PMID: 41673600 [PubMed - as supplied by publisher]
	Characterising cystic fibrosis in African populations: a scoping review protocol on phenotype, diagnosis, genetics and barriers to care. BMJ Open Ratner L, Marangu-Boore D, Hamouda S, Kwarteng Owusu S, Eze J, Dakshi A, Wordui S, Hamdy A, Owusu SA, Weldetsadik Y, Uluer A, Daimi H, El Makhzen N, Abriel H, Nasr S, Moosa S, Swanson C, Cronin AE, Zampoli M. PMID: 41667184 [PubMed - indexed for MEDLINE]
	Lung function outcomes of cystic fibrosis patients after early-life pulmonary exacerbations: National registry analysis. Pediatr Int Özkan Tabakç, Uytun S, Ery, Cinel G, Yalç, Kiper N, Akgül Erdal M, , Sava, Çelebi Ö, Ufuk Alt, Serbes M, Ayz, Çoku, Arslan H, Yazan H, Molla Kafi H, Çollak A, Ünal G, Y, Ça, Irmak I, Damado, Kartal Öztürk G, Demir E, Ba, Bingöl A, Can, Çekiç , Asfuro, Tana Aslan A, Harmanc, K, Köse M, Ersoy A, Hangül M, Özdemir A, Özcan G, Çobano, Gayretli Ayd, Keskin Ö, Yüksel H, Özdo, Topal E, Çaltepe G, Can D, Korkmaz Ekren P, K, , Pekcan S, Çak, Emiralio, Özçelik U, Do. PMID: 41660807 [PubMed - indexed for MEDLINE]
	Current drug hypersensitivity challenges facing patients with cystic fibrosis. J Cyst Fibros Gardner J, Clarke E, Peckham D, Whitaker P, Roehmel JF, Naisbitt DJ. PMID: 41654434 [PubMed - as supplied by publisher]
	Gut-lung microbial dynamics with lumacaftor/ivacaftor in children with cystic fibrosis: a prospective multicenter study. Pediatr Res Lussac-Sorton F, Narayana JK, Wizla N, Tatopoulos A, Baravalle M, Rotidis L, Houdoin V, Llerena C, Reix P, Sermet I, Languepin J, Charpentier E, Lefranc M, Alves Gomes P, Bui S, Beaufils F, Berger P, Chotirmall SH, Delhaes L, Enaud R. PMID: 41645021 [PubMed - as supplied by publisher]
	Impact of air pollution on lung function in cystic fibrosis over a decade in London: a UK CF Registry study. Thorax Saleem Khan M, Barratt B, Davies B, Simmonds NJ, Piel FB. PMID: 41644139 [PubMed - as supplied by publisher]
	Changes in the fungal ecology in the era of CFTR modulators: Results from a French multicenter study focused on cystic fibrosis airways. Med Mycol Lefranc M, Herault E, Bellanger AP, Guegan H, Imbert S, Enaud R, Bui S, Gabriel F, Accoceberry I, Yéra H, Scherer E, Vallet S, Héry-Arnaud G, Gangneux JP, Delhaes L. PMID: 41642246 [PubMed - as supplied by publisher]
	Detection of Pseudomonas aeruginosa in cystic fibrosis after initiation of CFTR modulators: a systematic review. Paediatr Respir Rev Terlizzi V, Timitilli E, Fiumara MS, Dolce D, Campana S, Chiappini E. PMID: 41638998 [PubMed - as supplied by publisher]
	Analysis of the Genome Aggregation Database (gnomAD) reveals a global burden of cystic fibrosis and the need for improved diagnosis and care. EBioMedicine Bar L, Darrah RJ, Vaidyanathan S. PMID: 41633103 [PubMed - as supplied by publisher]
	Comparison of preclinical drug efficacy in nasal and intestinal patient-derived models of cystic fibrosis. Eur J Pharmacol Latorre RV, Mortali C, Lotti V, Kleinfelder K, Melotti P, Sorio C. PMID: 41628661 [PubMed - as supplied by publisher]
	Effects of Elexacaftor Tezacaftor Ivacaftor on sinonasal imaging in children with cystic fibrosis. Rhinology Petit G, Coudert A, Hermann R, Truy E, Bonjour M, Reix P, Ayari S. PMID: 41627799 [PubMed - indexed for MEDLINE]
	MukoHelp: A self-help manual for patients with cystic fibrosis-Results from a randomized controlled trial. Acta Psychol (Amst) von Stackelberg C, Moritz S, Gabbert T, Miegel F. PMID: 41619375 [PubMed - as supplied by publisher]
	The Involvement of MicroRNAs in Innate Immunity and Cystic Fibrosis Lung Disease: A Narrative Review. Curr Issues Mol Biol Carbone A, Sajid N, Soccio P, Tondo P, Lacedonia D, Di Gioia S, Conese M. PMID: 41614888 [PubMed]
	Genetically engineered approaches to the treatment of cystic fibrosis. Biophys Rev Safrygina AA, Orlov YL. PMID: 41613863 [PubMed]
	Clinical effort against smoke exposure in cystic fibrosis (CEASE-CF): feasibility, acceptability, and preliminary efficacy. J Cyst Fibros Oates GR, Geurs R, Mims C, Gamble S, Juarez LD, Vandeberg BG, Ladores-Barrett S, Harris WT. PMID: 41611592 [PubMed - as supplied by publisher]
	Comparison of Stool Microbiome in Children with Cystic Fibrosis Treated with and Without Elexacaftor-Tezacaftor-Ivacaftor-A Pilot Study. Int J Mol Sci Sankararaman S, Liu R, Sun X, Retuerto M, Schindler T, Roesch E, Sferra TJ, Drumm M, Ghannoum M, Zhang L. PMID: 41596463 [PubMed - indexed for MEDLINE]

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