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Zystische Fibrose
15. November 2026
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Artikel 1 - 20 / 20300
Plethysmography as a Complementary Tool for Monitoring Response to CFTR Modulator Therapy in Children with Cystic Fibrosis: A Real-World Study.
J Clin Med
Postek MA, Walicka-Serzysko K, Borawska-Kowalczyk U, Milczewska J, Zybert K, Wo, Wo, Sands D.
PMID: 43030499 [PubMed]
Antisense Oligonucleotides as Quantitative Modulators of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): A Threshold-Based Therapeutic Framework for Class I and Class V CFTR Mutations.
BioDrugs
Battistini M, Lagostena L, Balestra D, Pinotti M, Baroni D.
PMID: 43024219 [PubMed - as supplied by publisher]
Prevalence of the F508del variant in patients with cystic fibrosis in northeastern Brazil: clinical and laboratory factors.
Respir Res Clin Pract
de Araújo EM, Silva CCE, Nogueira HBR, de Araújo LCB, Silveira LCB, Bessa OAAC.
PMID: 43017625 [PubMed - indexed for MEDLINE]
Pectoralis muscle features assessed by chest CT and their associations with clinical and functional outcomes in children and adolescents with cystic fibrosis: a cross-sectional study.
Respir Res Clin Pract
da Costa MS, Amor-Barbosa M, Sbruzzi M, Vendrusculo FM, Fischer DL, Carvalho FM, Andrade RGF, Pinto LA, Donadio MVF.
PMID: 43017613 [PubMed - indexed for MEDLINE]
Real-world outcomes of elexacaftor/tezacaftor/ivacaftor in a cohort of children and adolescents with cystic fibrosis in Brazil.
Respir Res Clin Pract
Cohen RWF, Coelho PF, Rocha LY, Moreira JVDC, Barboza N, Marins KAC, Meyer VMC, Costa PFBM, Folescu TW.
PMID: 43017612 [PubMed - indexed for MEDLINE]
Spontaneous clearance and real-world management after first asymptomatic MRSA isolation in pediatric cystic fibrosis.
BMC Pulm Med
Kavgac, Yalç, Sunman B, Kayao, Kantemir T, Emiralioglu N, Dogru D, Özçelik U.
PMID: 43015729 [PubMed - indexed for MEDLINE]
Longitudinal change in FEV(1) in adults with cystic fibrosis treated with elexacaftor-tezacaftor-ivacaftor in France: a prospective observational study.
Lancet Respir Med
Burgel PR, Lafourcade A, Da Silva J, Durieu I, Macey J, Danner-Boucher I, de Miranda S, Audousset C, Murris-Espin M, Renaud-Picard B, Morisse-Pradier H, Hamidfar R, Chiron R, Guillaumot A, Belleguic C, Mely L, Reynaud-Gaubert M, Mankikian J, Ramel S, Fanton A, Priou P, Montcouquiol S, Leroy S, Richaud-Thiriez B, Douvry B, Mulette P, Arnouat B, Dupuy-Grasset M, Campbell K, Choinier P, Boldron A, Poulet C, Allou N, Bessou A, Martin C, French Cystic Fibrosis Reference Network study group.
PMID: 43014331 [PubMed - as supplied by publisher]
Cystic fibrosis: remarkable success but still not at the finish line.
Proc (Bayl Univ Med Cent)
Jung F, Rosenblatt R.
PMID: 43013617 [PubMed - as supplied by publisher]
Digital health in cystic fibrosis across the eHealth life-cycle: why successful innovation requires more than randomised trials.
Breathe (Sheff)
Vagg T, Roukema J, Edmondson C, Albon D, Ranganathan SC, Plant BJ.
PMID: 43011906 [PubMed]
SGLT1 inhibition in cystic fibrosis: From preclinical evidence to clinical potential.
Mol Ther Adv
Liang X, Liu Y, Jia S, Zhang K, Xu J.
PMID: 42999678 [PubMed]
Factors Guiding Gastrostomy Tube Decision-Making for Caregivers of Children With Cystic Fibrosis: A Scoping Review.
Pediatr Pulmonol
Rahimian A, Givens N, Godfrey C, Goebel K, Ohamadike C, Dickinson KM.
PMID: 42997966 [PubMed - indexed for MEDLINE]
Health-Related Quality of Life and Preference-Based Utility Index in People With Cystic Fibrosis Receiving Elexacaftor/Tezacaftor/Ivacaftor: A National Registry Study.
Pediatr Pulmonol
Hegelund MH, Bryrup T, Henriksen EH, Højte C, Katzenstein TL, Jeppesen M, Qvist T, Olesen HV, Olsen MF, TransformCF Study Group.
PMID: 42995692 [PubMed - indexed for MEDLINE]
Cystic Fibrosis in Egypt.
Pediatr Pulmonol
Nasr SZ, Fleifil S, Fouda E, Kamel TB, Ali HA, Naguib ML, ElAttar MM, Elbasha NRM, Taha O, Sarhan DT, Tamer D, Regal MEE, Elmeazawy R, Fasseeh N, Libik MM, Macek M Jr.
PMID: 42995683 [PubMed - indexed for MEDLINE]
Understanding Quality of Life in Pediatric Cystic Fibrosis: Insights From a Multicenter Cohort Study Across Colombia.
Pediatr Pulmonol
Dueñas-Meza E, De la Hoz-Diaz Granados DC, Proaños NJ, Pulido S, Portella T, Jurado J, Giraldo-Cadavid LF.
PMID: 42995682 [PubMed - indexed for MEDLINE]
Current knowledge, key gaps, and opportunities for future research on high-impact, modifiable lifestyle behaviors to promote healthy aging in adults with cystic fibrosis in the era of modulator therapy.
J Cyst Fibros
Bathgate CJ, Riekert KA, Fedele DA, Everhart RS, Dickinson KM, Saavedra MT, Oates GR, Russell KA, Cravens R, Frederick CA.
PMID: 42995032 [PubMed - as supplied by publisher]
Changes in neuropsychiatric symptoms after switching from elexacaftor/tezacaftor/ivacaftor to vanzacaftor/tezacaftor/deutivacaftor: A single-center experience.
Respir Med
Galipean J, Hadjiliadis D, Kane S, Longacre W, Hong G.
PMID: 42994765 [PubMed - indexed for MEDLINE]
Mucus Plugging Across Multiple Chronic Respiratory Diseases: A Systematic Review and Meta-analysis.
Lung
Du D, Liu S, Zhang Y, Gao L, Zeng T, An N, Chen F, Luo F, Shen Y.
PMID: 42993210 [PubMed - indexed for MEDLINE]
The Association Between Meconium Ileus and Nutritional and Pulmonary Outcomes in Children With Cystic Fibrosis.
Pediatr Pulmonol
Sanders DB, Shah Y, Cordova JMG, Saunders JL, Ren CL, Owora AH.
PMID: 42978396 [PubMed - indexed for MEDLINE]
Assessing infection and inflammation in people with cystic fibrosis using their breath: A pilot longitudinal study.
J Breath Res
Gao A, Ackah-Cudjoe J, Hashemi M, Durfey S, Mckone EF, Wagner BD, Singh PK, Hill JE.
PMID: 42976381 [PubMed - as supplied by publisher]
Integrating US Registry data to reveal social and environmental determinants impacting lung function decline in cystic fibrosis patients.
J Appl Stat
Andrinopoulou ER, Gecili E, Szczesniak RD.
PMID: 42974119 [PubMed]
Artikel 1 - 20 / 20300
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