medline.ch Respirationstrakt Zystische Fibrose

	Cellular Models and Functional Assays for Assessing CFTR Function: A Comprehensive Review. Int J Mol Sci Lopatina M, Demchenko A, Smirnikhina S. PMID: 42353213 [PubMed - indexed for MEDLINE]
	Aspergillus spp. in Non-Cystic Fibrosis Bronchiectasis: Clinical Phenotypes, Molecular Endotypes, and Practical Management-A Narrative Review. Int J Mol Sci Bertuccio FR, Pisanu L, Arminio M, Arlando L, Tafa M, Cosseta Reposi P, Gallo E, Asperges E, Valsecchi P, Cascina A, Corsico AG, Conio V, Stella GM. PMID: 42352989 [PubMed - indexed for MEDLINE]
	Impact of Highly Effective CFTR Modulator Therapy on Physical Activity, Sleep, and Sinonasal Symptoms in Preschool Children with Cystic Fibrosis: A Prospective Single-Center Pilot Study. Adv Respir Med Schellhorn S, Schmidt H, Janda A, Gülke D, Toth M, Fabricius D, Bode SFN. PMID: 42345641 [PubMed - indexed for MEDLINE]
	Inflammation and oxidative stress in the sputum of patients with cystic fibrosis: correlations with lung function, aerobic fitness, and morbidity. Rev Paul Pediatr Fischer DL, Vendrusculo FM, Costa MSD, Garcia MCR, Oliveira JR, Donadio MVF. PMID: 42340004 [PubMed - indexed for MEDLINE]
	Changes in chronic therapies for cystic fibrosis following initiation of CFTR modulators: A UK retrospective cohort study 2009 - 2023. J Cyst Fibros Busby J, McKeever TM, Fogarty AW, Barr HL. PMID: 42336706 [PubMed - as supplied by publisher]
	Non-cystic Fibrosis and Non-tuberculosis Sequela Bronchiectasis. Thorac Surg Clin Fonini JS, Watzka SB. PMID: 42336507 [PubMed - indexed for MEDLINE]
	No Place Like Home: Home Spirometry for Cystic Fibrosis Clinical Trials. Ann Am Thorac Soc Donaldson SH. PMID: 42334938 [PubMed - as supplied by publisher]
	Feasibility and Tolerance of High-Intensity Interval Training in Adults With Cystic Fibrosis. Arch Rehabil Res Clin Transl Mely L, Meurisse O, Norberciak L, Auffret M, Goriot-Raynaud N, Buyse M, Ramel S. PMID: 42326570 [PubMed]
	Redox Profile, Inflammatory and Cardiac Autonomic Nervous Activity of Children and Adolescents With Cystic Fibrosis. Pediatr Int de França ACL, Ribeiro MD, Meireles ACF, Toscano LT, Maia LA, Cartaxo CGB, Araújo GDCB, Gonçalves MDCR, Alves JLB, Silva AS. PMID: 42324496 [PubMed - indexed for MEDLINE]
	Microbial and host innate immune factors affecting the persistence of Staphylococcus aureus in cystic fibrosis airways. Front Cell Infect Microbiol Fairholm JD, Paul GT, Birket S, Rada B. PMID: 42318016 [PubMed - indexed for MEDLINE]
	Safety and efficacy of elexacaftor/tezacaftor/ivacaftor in children â‰¥2 years with cystic fibrosis: 96-week interim results from a phase 3 open-label extension study. J Cyst Fibros Goralski JL, Daines C, Pittman JE, Rayment JH, Robinson P, Thursfield R, Stehling F, Ratjen F, Ahluwalia N, Shi P, Lu M, Weinstock TG, Mall MA, VX20-445-112 Study Group. PMID: 42315414 [PubMed - as supplied by publisher]
	Persistence of lung hyperinflation and small airway dysfunction in school-aged children with cystic fibrosis treated with elexacaftor-tezacaftor-ivacaftor: results from the real-world MODUL-CF study. ERJ Open Res Colin L, Delaup V, Le Bourgeois M, Neve V, Wizla-Derambure N, Ioan IC, Tatopoulos A, Kieffer S, Blonde A, Bokov P, Houdoin V, Le Clainche L, Barzic A, Ohlmann C, Toin T, Perrin T, Coutier L, Abou Taam R, Bonnel AS, Rignani A, Feghali H, Bui S, Fayon M, Letierce A, Sermet-Gaudelus I, Reix P. PMID: 42311871 [PubMed]
	Screen time and pulmonary function in hospitalized children with cystic fibrosis. J Bras Pneumol Rodrigues VDS, Schmidt C, Medeiros GK, Affeldt GH, Ziegler B. PMID: 42307338 [PubMed - indexed for MEDLINE]
	The role of ultrasound of the quadriceps femoris in people with cystic fibrosis: a systematic review and meta-analysis. J Bras Pneumol Sernaglia JEC, Souza AP, Gonçalves AC, Borgli DSP, Gomez CCS, Ribeiro JD. PMID: 42307335 [PubMed - indexed for MEDLINE]
	A feasibility pilot trial to deliver a virtual intervention for promoting daily self-management in adolescents and young adults with cystic fibrosis: A brief report of tele-coach outcomes. PEC Innov Lindwall JJ, Muther EF, Ford C, Bord E, Green A, Polineni D, Naranjo D, Duncan CL. PMID: 42305635 [PubMed]
	Surfactant-driven quorum sensing of Pseudomonas aeruginosa in cystic fibrosis. AMB Express Selvamani P, John J, Kumar JD, Gopalakrishnan S, Mangu JCK, Thangaraj P, Parthasarathy K. PMID: 42301374 [PubMed - as supplied by publisher]
	Real-Life Experience With a Generic Formulation of Elexacaftor/Tezacaftor/Ivacaftor in Patients With Cystic Fibrosis With Responding Variants. Pediatr Pulmonol Teper A, Rodríguez V, Lubovich S, Zaragoza S, Rodríguez Novoa E, García Bournissen F. PMID: 42299466 [PubMed - indexed for MEDLINE]
	ORIGIN-1 trial: study protocol for an organoid-guided N-of-1 trial evaluating CFTR modulator response in cystic fibrosis with rare non-F508del mutations. Trials Sabino LR, Kaiko GE, Dorahy D, Goodsall T, Jaffe A, Schultz A, Waters S, Cook D, Kok H, Tong K, Totterdell J, McGree J, Snelling T, Wark PAB. PMID: 42298697 [PubMed - as supplied by publisher]
	Remodeling the pathological airway: advanced nanotechnology for diagnostics and therapeutics in cystic fibrosis. J Nanobiotechnology Zou Y, Zhao H, Feng M, Wu Z, Cao Z, Fan Z, Gluchman M, Yang H, Zhao C, Yu P, Zhang X. PMID: 42298581 [PubMed - as supplied by publisher]
	A qualitative study on the experiences and perspectives of adults with cystic fibrosis and healthcare professionals. Respir Med Akyazi N, Kemer SN, Yagli NV, Saglam M, Damadoglu E, Karcioglu O, Bilgin S. PMID: 42297157 [PubMed - indexed for MEDLINE]

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