medline.ch Respirationstrakt Zystische Fibrose

	AI-driven risk prediction andÂ categorization inÂ cystic fibrosis leveraging AttentiveLSTM andÂ Fox Wolf Optimizer. Stat Appl Genet Mol Biol Pandagale AA, Patil LV. PMID: 41698853 [PubMed - indexed for MEDLINE]
	Correction: Safety, feasibility and efficacy of exercise as an airway clearance technique in cystic fibrosis: a randomised pilot feasibility trial. Thorax PMID: 41698815 [PubMed - in process]
	Co-design, implementation, and evaluation of a nested diabetes model of care for adults with cystic fibrosis: a mixed methods pre-post implementation study. JBI Evid Implement Kumar S, Smith D, Moore V, Matson A. PMID: 41697190 [PubMed - as supplied by publisher]
	Adult Ileocolic Intussusception in a Patient With Cystic Fibrosis: Diagnostic Role of Point-of-Care Ultrasound 'Case Report'. Australas J Ultrasound Med Al Khalifah A, Aldawood A. PMID: 41696671 [PubMed]
	A retrospective cohort study evaluating the growth and clinical outcomes of preterm and term infants with cystic fibrosis during the first 11 years of life. JPGN Rep Reda H, Ahmed S, Sturza J, Nasr SZ. PMID: 41695059 [PubMed]
	How Should IgG Seroconversion to Aspergillus fumigatus be Interpreted in Children With Cystic Fibrosis. Can Respir J Petat H, Costa D, Lubrano M, Couderc L, Marguet C. PMID: 41694025 [PubMed - indexed for MEDLINE]
	Endocrine care during transition in emerging adults with cystic fibrosis: a single center retrospective study. Endocr Pract Cobb C, Feeley J, Nilo G Binongo J, Hunt WR, Daley T, Linnemann RW, Stecenko A, Tangpricha V. PMID: 41690586 [PubMed - as supplied by publisher]
	Sputum Biomarkers of Inflammation to Track Acute Respiratory Events in School-Age Children with Cystic Fibrosis. Int J Mol Sci Ben-Meir E, Perrem L, Nissen G, Shaw M, Ratjen F, Grasemann H. PMID: 41684034 [PubMed - indexed for MEDLINE]
	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 multicentre 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 - indexed for MEDLINE]
	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]

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