medline.ch Respirationstrakt Zystische Fibrose

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Sie sind hier: Respirationstrakt » Zystische Fibrose

17. Mai 2022

Kardiovaskuläre Erkrankungen

Muskuloskelettale Erkrankungen

Allergische Rhinitis - Pollinosis

Asthma

Bronchitis

COPD

Interstitielle Pneumopathien

Schlaf- Apnoe-Syndrom

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	Artikel 1 - 20 / 17001

	An Update on CFTR Modulators as New Therapies for Cystic Fibrosis. Paediatr Drugs King JA, Nichols AL, Bentley S, Carr SB, Davies JC. PMID: 35570261 [PubMed - as supplied by publisher]
	Renal Function in Patients with Cystic Fibrosis: A Single-Center Study. Int J Environ Res Public Health Rachel M, Galiniak S, Biesiadecki M, Gala-B. PMID: 35564849 [PubMed - in process]
	Limitations of standard cost-effectiveness methods for health technology assessment of treatments for rare, chronic diseases: a case study of treatment for cystic fibrosis. J Med Econ Rubin JL, Lopez A, Booth J, Gunther P, Jena AB. PMID: 35549639 [PubMed - as supplied by publisher]
	Telemedicine of patients with cystic fibrosis during the COVID-19 pandemic. Rev Paul Pediatr Costa RLF, Costa RF, Gonçalves CP, Cohen RWF, Santana NN. PMID: 35544907 [PubMed - indexed for MEDLINE]
	Prevalence and subtyping of biofilms present in bronchoalveolar lavage from children with protracted bacterial bronchitis or non-cystic fibrosis bronchiectasis: a cross-sectional study. Lancet Microbe Marsh RL, Binks MJ, Smith-Vaughan HC, Janka M, Clark S, Richmond P, Chang AB, Thornton RB. PMID: 35544075 [PubMed - in process]
	Short-Term Effects of Elexacaftor/Tezacaftor/Ivacaftor Combination on Glucose Tolerance in Young People With Cystic Fibrosis-An Observational Pilot Study. Front Pediatr Korten I, Kieninger E, Krueger L, Bullo M, Flück CE, Latzin P, Casaulta C, Boettcher C. PMID: 35529332 [PubMed]
	The impact of FDA and EMA regulatory decision-making process on the access to CFTR modulators for the treatment of cystic fibrosis. Orphanet J Rare Dis Costa E, Girotti S, Pauro F, Leufkens HGM, Cipolli M. PMID: 35525974 [PubMed - indexed for MEDLINE]
	Systematic review on fecal calprotectin in cystic fibrosis. J Pediatr (Rio J) Lazzarotto ES, Vasco JFM, Führ F, Riedi CA, Filho NAR. PMID: 35523321 [PubMed - as supplied by publisher]
	Alterations in innate immune responses of patients with chronic rhinosinusitis related to cystic fibrosis. PLoS One Rezende GL, Nakanishi M, Couto SCP, Martins CLFS, Sampaio ALL, Albuquerque LFF, Kückelhaus SAS, Muniz-Junqueira MI. PMID: 35522627 [PubMed - indexed for MEDLINE]
	A dual center and dual vendor comparison study of automated perfusion-weighted phase-resolved functional lungÂ magnetic resonance imaging with dynamic contrast-enhanced magnetic resonance imaging in patients with cystic fibrosis. Pulm Circ Behrendt L, Smith LJ, Voskrebenzev A, Klime, Kaireit TF, Pöhler GH, Kern AL, Gonzalez CC, Dittrich AM, Marshall H, Schütz K, Hughes PJC, Ciet P, Tiddens HAWM, Wild JM, Vogel-Claussen J. PMID: 35514781 [PubMed]
	Blood mRNA biomarkers distinguish variable systemic and sputum inflammation at treatment initiation of inhaled antibiotics in cystic fibrosis: A prospective non-randomized trial. PLoS One Caceres SM, Sanders LA, Rysavy NM, Poch KR, Jones CR, Pickard K, Fingerlin TE, Marcus RA, Malcolm KC, Taylor-Cousar JL, Nichols DP, Nick JA, Strand M, Saavedra MT. PMID: 35511761 [PubMed - indexed for MEDLINE]
	Impacts of Nontuberculous Mycobacteria Isolates in Non-cystic Fibrosis Bronchiectasis: A 16-Year Cohort Study in Taiwan. Front Microbiol Lin CY, Huang HY, Hsieh MH, Fang YF, Lo YL, Lin SM, Huang YT, Yeh CH, Wang CH, Lin HC. PMID: 35509319 [PubMed]
	Angiographic and histopathological study on bronchial-to-pulmonary vascular anastomoses on explants from patients with cystic fibrosis after bronchial artery embolisation. J Cyst Fibros Habert P, Puech B, Coiffard B, Secq V, Thomas P, Bec R, Vidal V, Mancini J, Bermudez J, Reynaud-Gaubert M, Gaubert JY. PMID: 35508453 [PubMed - as supplied by publisher]
	Cystic Fibrosis and Diagnostic Imaging. Radiol Technol Fichthorn C. PMID: 35508411 [PubMed - indexed for MEDLINE]
	[Extreme electrolyte depletion associated with septic shock as a form of presentation of cystic fibrosis]. Andes Pediatr Ampuero Acuña C, Tomarelli Rubio G, Montes Franceschini S, Donoso Fuentes A. PMID: 35506784 [PubMed - indexed for MEDLINE]
	Cystic fibrosis and alpha-1 antitrypsin deficiency: case report and review of literature. BMC Pediatr Jaspers E, Van Dijck I, Hoffman I, Knops N, Stéphenne X, Witters P, Proesmans M. PMID: 35505316 [PubMed - indexed for MEDLINE]
	CFTR protein quantification as a cystic fibrosis diagnostic biomarker in dried blood spots using multiple reaction monitoring tandem mass spectrometry. J Pharm Biomed Anal Sumaily KM, Nimer R, Alzahrani M, Abdel Jabar M, Alodib A, Sabi EM, Nizami I, Abdel Rahman AM. PMID: 35504217 [PubMed - as supplied by publisher]
	Cystic fibrosis year in review 2021. Pediatr Pulmonol Savant AP. PMID: 35501666 [PubMed - as supplied by publisher]
	Results of Lung Transplantations Among Cystic Fibrosis Patients: A Single-Center Study. Transplant Proc Urlik M, St, Latos M, N, Zawadzki F, Pasek P, Przyby, Ochman M. PMID: 35501172 [PubMed - as supplied by publisher]
	Role of Cellular Metabolism in the Formation of Neutrophil Extracellular Traps in Airway Diseases. Front Immunol Morán G, Uberti B, Quiroga J. PMID: 35493475 [PubMed - indexed for MEDLINE]

Artikel 1 - 20 / 17001

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