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Year Number of Results
2019 3
2020 5
2021 5
2022 6
2023 7
2024 1

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24 results

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Page 1
Inhaled medications in cystic fibrosis beyond antibiotics.
Sepe A, Villella VR, Cimbalo C, Castaldo A, Nunziata F, Corcione A, Bona G, Maiuri L, Raia V. Sepe A, et al. Among authors: castaldo a. Minerva Pediatr. 2019 Aug;71(4):371-375. doi: 10.23736/S0026-4946.19.05509-9. Epub 2019 Feb 13. Minerva Pediatr. 2019. PMID: 30761821 Review.
Lung Microbiome as a Treatable Trait in Chronic Respiratory Disorders.
Scialò F, Vitale M, D'Agnano V, Mariniello DF, Perrotta F, Castaldo A, Campbell SFM, Pastore L, Cazzola M, Bianco A. Scialò F, et al. Among authors: castaldo a. Lung. 2023 Oct;201(5):455-466. doi: 10.1007/s00408-023-00645-3. Epub 2023 Sep 26. Lung. 2023. PMID: 37752217 Review.
MIS-C: A COVID-19-as sociated condition between hypoimmunity and hyperimmunity.
Gelzo M, Castaldo A, Giannattasio A, Scalia G, Raia M, Esposito MV, Maglione M, Muzzica S, D'Anna C, Grieco M, Tipo V, La Cava A, Castaldo G. Gelzo M, et al. Among authors: castaldo a. Front Immunol. 2022 Oct 3;13:985433. doi: 10.3389/fimmu.2022.985433. eCollection 2022. Front Immunol. 2022. PMID: 36263058 Free PMC article.
Lipidomic alterations in human saliva from cystic fibrosis patients.
Caterino M, Fedele R, Carnovale V, Castaldo A, Gelzo M, Iacotucci P, Ruoppolo M, Castaldo G. Caterino M, et al. Among authors: castaldo a. Sci Rep. 2023 Jan 12;13(1):600. doi: 10.1038/s41598-022-24429-6. Sci Rep. 2023. PMID: 36635275 Free PMC article.
Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype.
Tosco A, Castaldo A, Colombo C, Claut L, Carnovale V, Iacotucci P, Lucarelli M, Cimino G, Fabrizzi B, Caporelli N, Majo F, Ciciriello F, Padoan R, Poli P, Taccetti G, Centrone C, Casciaro R, Castellani C, Salvatore D, Colangelo C, Bonomi P, Castaldo G, Terlizzi V. Tosco A, et al. Among authors: castaldo a. J Cyst Fibros. 2022 Sep;21(5):850-855. doi: 10.1016/j.jcf.2022.04.020. Epub 2022 May 4. J Cyst Fibros. 2022. PMID: 35523714
A complicated association between two different genetic rare disorders: cystic fibrosis and spinal muscular atrophy.
Palma M, Spadarella S, Donnarumma B, Zollo G, Nunziata F, Cimbalo C, Castaldo A, Buonpensiero P, Terrone G, Varone A, Tosco A, Sepe A, Raia V. Palma M, et al. Among authors: castaldo a. Minerva Pediatr (Torino). 2022 Dec;74(6):797-799. doi: 10.23736/S2724-5276.19.05614-7. Epub 2021 Apr 2. Minerva Pediatr (Torino). 2022. PMID: 33820398 No abstract available.
The Role of Bronchoscopy in the Management of Children With Cystic Fibrosis.
Tosco A, Poli P, Casale A, De Gregorio F, Sepe A, Buonpensiero P, Di Pasqua A, Castaldo A, Cimbalo C, Buzzetti R, Raia V, Berlucchi M, Timpano S, Badolato R, Padoan R, Orlando C. Tosco A, et al. Among authors: castaldo a. J Bronchology Interv Pulmonol. 2023 Jul 1;30(3):258-267. doi: 10.1097/LBR.0000000000000874. J Bronchology Interv Pulmonol. 2023. PMID: 35698279
24 results