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Elexacaftor/Tezacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for the F508del Mutation and Advanced Lung Disease: A 48-Week Observational Study.
Carnovale V, Iacotucci P, Terlizzi V, Colangelo C, Ferrillo L, Pepe A, Francalanci M, Taccetti G, Buonaurio S, Celardo A, Salvadori L, Marsicovetere G, D'Andria M, Ferrara N, Salvatore D. Carnovale V, et al. Among authors: pepe a. J Clin Med. 2022 Feb 16;11(4):1021. doi: 10.3390/jcm11041021. J Clin Med. 2022. PMID: 35207295 Free PMC article.
Elexacaftor/tezacaftor/ivacaftor for CFTR variants giving rise to diagnostic uncertainty: Personalised medicine or over-medicalisation?
Salvatore D, Pepe A, Carnovale V, Majo F, Padoan R, Quattrucci S, Salvatore M, Taruscio D, Amato A, Ferrari G, Campagna G. Salvatore D, et al. Among authors: pepe a. J Cyst Fibros. 2022 May;21(3):544-548. doi: 10.1016/j.jcf.2021.09.011. Epub 2021 Sep 25. J Cyst Fibros. 2022. PMID: 34583889 Free article. No abstract available.
Elexacaftor/tezacaftor/ivacaftor in children aged 6-11 years with cystic fibrosis, at least one F508DEL allele, and advanced lung disease: A 24-week observational study.
Salvatore D, Cimino G, Troiani P, Bignamini E, Esposito I, Leonetti G, Zanda M, Manunza D, Pepe A. Salvatore D, et al. Among authors: pepe a. Pediatr Pulmonol. 2022 Sep;57(9):2253-2256. doi: 10.1002/ppul.25980. Epub 2022 May 25. Pediatr Pulmonol. 2022. PMID: 35577767 No abstract available.
582 results