Long-term effectiveness of dual CFTR modulator treatment of cystic fibrosis
暂无分享,去创建一个
M. Bannier | M. Eijkemans | R. Hoek | J. Altenburg | V. Gulmans | H. Janssens | M. Nuijsink | H. Heijerman | L. Conemans | G. Koppelman | D. Muilwijk | C. van der Ent | R. van der Meer | J. Noordhoek | D. Z. Zomer-van Ommen | K. M. de Winter–de Groot | Suzanne W. J. Terheggen-Lagro | H. van der Vaart | M. Bakker | J. S.W.J. H.G.M. K.M. M. R.A.S. H.M. R. M. H. G.H. L. Altenburg Terheggen-Lagro Heijerman de Winter-
[1] Rutger M van den Bor,et al. Prediction of Real-World Long-Term Outcomes of People with CF Homozygous for the F508del Mutation Treated with CFTR Modulators , 2021, Journal of personalized medicine.
[2] J. Beekman,et al. A new era for people with cystic fibrosis , 2021, European Journal of Pediatrics.
[3] R. Enaud,et al. Long-Term Outcomes in Real Life of Lumacaftor-Ivacaftor Treatment in Adolescents with Cystic Fibrosis , 2021, SSRN Electronic Journal.
[4] J. Clancy,et al. Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial , 2021, Annals of the American Thoracic Society.
[5] T. Kotsimbos,et al. Lumacaftor/ivacaftor-associated health stabilisation in adults with severe cystic fibrosis , 2020, ERJ Open Research.
[6] T. Kotsimbos,et al. Lung function over the life course of paediatric and adult patients with cystic fibrosis from a large multi-centre registry , 2020, Scientific Reports.
[7] M. Moustaki,et al. Longitudinal changes in lung function following initiation of lumacaftor/ivacaftor combination. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[8] A. Salvator,et al. Practitioner Due Diligence: Real-World Lumacaftor/Ivacaftor Use. , 2020, The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG.
[9] S. Rowe,et al. Females with Cystic Fibrosis Demonstrate a Differential Response Profile to Ivacaftor Compared to Males. , 2019, American journal of respiratory and critical care medicine.
[10] K. De Boeck,et al. Year to year change in FEV1 in patients with cystic fibrosis and different mutation classes. , 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[11] C. Goss,et al. Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): a phase 3, extension study. , 2017, The Lancet. Respiratory medicine.
[12] Xiaohong Huang,et al. Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR. , 2015, The New England journal of medicine.
[13] P. Negulescu,et al. Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809 , 2011, Proceedings of the National Academy of Sciences.
[14] P. Negulescu,et al. Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770 , 2009, Proceedings of the National Academy of Sciences.