medline.ch Respirationstrakt Zystische Fibrose

	Offering reproductive genetic carrier screening for cystic fibrosis, spinal muscular atrophy and fragile X syndrome: Views of Victorian general practitioners. Aust J Gen Pract Leibowitz R, Lewis S, Delatycki M, Massie J, Emery J, Archibald A. PMID: 39693757 [PubMed - indexed for MEDLINE]
	A Global Perspective on Transition Models for Pediatric to Adult Cystic Fibrosis Care: What Has Been Made So Far? J Clin Med Poamaneagra SC, Plesca DA, Tataranu E, Marginean O, Nemtoi A, Mihai C, Gilca-Blanariu GE, Andronic CM, Anchidin-Norocel L, Diaconescu S. PMID: 39685886 [PubMed]
	The Impact of Complementary Feeding on Fecal Microbiota in Exclusively Breast-Fed Infants with Cystic Fibrosis (A Descriptive Study). Nutrients Asensio-Grau A, Garriga M, Vicente S, Andrés A, Ribes-Koninckx C, Calvo-Lerma J. PMID: 39683464 [PubMed - indexed for MEDLINE]
	Advancing the Battle against Cystic Fibrosis: Stem Cell and Gene Therapy Insights. Curr Med Sci Shah DD, Chorawala MR, Pandya AJ, Kothari N, Prajapati BG, Parekh PS. PMID: 39676146 [PubMed - as supplied by publisher]
	Antibiotic treatment of bacterial lung infections in cystic fibrosis. Eur J Pediatr Taccetti G, Terlizzi V, Campana S, Dolce D, Ravenni N, Fevola C, Francalanci M, Galici V, Neri AS. PMID: 39672981 [PubMed - indexed for MEDLINE]
	Pregnancy in People With Cystic Fibrosis Treated With Highly Effective Modulator Therapy. Obstet Gynecol Goralski JL, Talati AN, Hardisty EE, Vora NL. PMID: 39666984 [PubMed - indexed for MEDLINE]
	Systematic Review and Meta-Analysis on the Prevalence and Antibiotic Susceptibility Pattern in Pseudomonas aeruginosa Isolated from Cystic Fibrosis Patients. Eurasian J Med Rastegar-Kashkouli A, Khaledi A, Moammer F, Ghenaatpisheh Sanani M, Mahdi Heidari M, Foroughi Eghbal A. PMID: 39655837 [PubMed]
	Sinus mucocele leads to unilateral proptosis in an infant patient with cystic fibrosis: a literature review and a case report study. Ann Med Surg (Lond) Lashkarbolouk N, Mazandarani M, Biazar P, Shahkar L. PMID: 39649888 [PubMed]
	Addressing pain in people living with cystic fibrosis: Cystic fibrosis foundation evidence-informed guidelines. J Cyst Fibros Dellon EP, Allada G, Allgood SJ, Georgiopoulos AM, Goggin JL, Hadjiliadis D, Lowman JD, Madge S, Middour-Oxler B, Muirhead C, Noel M, Wilson P, Se H, Faro A, Kavalieratos D, Committee on Pain in CF.. PMID: 39645476 [PubMed - as supplied by publisher]
	Changing profile of bacterial infection and microbiome in cystic fibrosis: when to use antibiotics in the era of CFTR-modulator therapy. Eur Respir Rev Milczewska J, Syunyaeva Z, , Sands D, Thee S. PMID: 39631927 [PubMed - indexed for MEDLINE]
	Daily variability of Pseudomonas aeruginosa density in cystic fibrosis sputum. J Cyst Fibros Carmody LA, Caverly LJ, Kalikin LM, Thornton CS, Simon RH, VanDevanter DR, LiPuma JJ. PMID: 39627109 [PubMed - as supplied by publisher]
	ACT with CF: A randomized trial of acceptance and commitment therapy vs supportive psychotherapy for adults with cystic fibrosis. Gen Hosp Psychiatry O'Hayer CV, Smith PJ, Drescher CF, Bruschwein H, Nurse CN, Kushner HM, Ingle K, Stephen MJ, Hoag JB. PMID: 39626332 [PubMed - indexed for MEDLINE]
	Accuracy, Reproducibility, and Responsiveness to Treatment of Home Spirometry in Cystic Fibrosis: Multicenter, Retrospective, Observational Study. J Med Internet Res Oppelaar MC, van Helvoort HA, Bannier MA, Reijers MH, van der Vaart H, van der Meer R, Altenburg J, Conemans L, Rottier BL, Nuijsink M, van den Wijngaart LS, Merkus PJ, Roukema J. PMID: 39626236 [PubMed - indexed for MEDLINE]
	Predictors of frequency of CF care in the US Cystic Fibrosis Foundation Patient Registry. PLoS One Hinton AC, Sears EH, Zuckerman JB, Lopez-Pintado S. PMID: 39625878 [PubMed - indexed for MEDLINE]
	Expanding the Impact of New Cystic Fibrosis Therapies in Low- and Middle-Income Countries. Pediatr Pulmonol Kerem E. PMID: 39625248 [PubMed - as supplied by publisher]
	Fatty acid abnormalities in cystic fibrosis-the missing link for a cure? iScience Drzyma, Walkowiak J, Colombo C, Alicandro G, Storrösten OT, Kolsgaard M, Bakkeheim E, Strandvik B. PMID: 39620135 [PubMed]
	Measurement of treatment burden in cystic fibrosis: A systematic review. J Cyst Fibros Altabee R, Mwamba MJ, Turner D, Davies G, Abbott J, Simmonds NJ, Whitty JA, Carr SB, Barton G, Cameron RA. PMID: 39616120 [PubMed - as supplied by publisher]
	Lung Clearance Index Improves in People with Cystic Fibrosis not Achieving a Clinical Important Difference in Forced Expiratory Volume in One Second After Elexacaftor/Tezacaftor/Ivacaftor Therapy. Lung Daccò V, Gramegna A, Rosazza C, Mariani A, Biffi A, Lanfranchi C, Zazzeron L, Bellante F, Blasi F, Alicandro G. PMID: 39614886 [PubMed - indexed for MEDLINE]
	Using X-ray velocimetry to measure lung function and assess the efficacy of a pseudomonas aeruginosa bacteriophage therapy for cystic fibrosis. Sci Rep Harker SA, Preissner M, Chang RY, Trevascus D, Liu C, Wang Y, Chow MYT, Cmielewski P, Reyne N, How YY, Pollock JA, Klein M, Wright CA, Dubsky S, Donnelley M, Chan HK, Morgan KS. PMID: 39614107 [PubMed - indexed for MEDLINE]
	Host DNA depletion on frozen human respiratory samples enables successful metagenomic sequencing for microbiome studies. Commun Biol Kim M, Parrish RC 2nd, Tisza MJ, Shah VS, Tran T, Ross M, Cormier J, Baig A, Huang CY, Brenner L, Neuringer I, Whiteson K, Harris JK, Willis AD, Lai PS. PMID: 39609616 [PubMed - indexed for MEDLINE]

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