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Characterization of CFTR mutations in people with cystic fibrosis and severe liver disease who are not eligible for CFTR modulators.
Colombo C, Ramm GA, Lindblad A, Corti F, Porcaro L, Alghisi F, Asherova I, Evans H, Kashirskaya N, Kondratyeva E, Lewindon PJ, de Monestrol I, Oliver M, Ooi CY, Padoan R, Shankar S, Alicandro G. Colombo C, et al. Among authors: alghisi f. J Cyst Fibros. 2023 Mar;22(2):263-265. doi: 10.1016/j.jcf.2023.01.012. Epub 2023 Feb 2. J Cyst Fibros. 2023. PMID: 36739240
[Testis cancer markers. Clinical use].
Salesi N, Di Cocco B, Alghisi F, Calabretta F, Bossone G. Salesi N, et al. Among authors: alghisi f. Minerva Med. 2002 Oct;93(5):365-9. Minerva Med. 2002. PMID: 12410169 Review. Italian.
[Hamartomatous polyposis syndromes].
Bossone G, Salesi N, Alghisi F, Di Cocco B. Bossone G, et al. Among authors: alghisi f. Recenti Prog Med. 2004 Feb;95(2):101-3. Recenti Prog Med. 2004. PMID: 15072395 Review. Italian.
Growth assessment of paediatric patients with CF comparing different auxologic indicators: A multicentre Italian study.
Lucidi V, Alghisi F, Raia V, Russo B, Valmarana L, Valmarana R, Coruzzo A, Beschi S, Dester S, Rinaldi D, Maglieri M, Guidotti ML, Ravaioli E, Pesola M, De Alessandri A, Padoan R, Grynzich L, Ratclif L, Repetto T, Ambroni M, Provenzano E, Tozzi AE, Colombo C. Lucidi V, et al. Among authors: alghisi f. J Pediatr Gastroenterol Nutr. 2009 Sep;49(3):335-42. doi: 10.1097/MPG.0b013e31818f0a39. J Pediatr Gastroenterol Nutr. 2009. PMID: 19543116
Defining research priorities in cystic fibrosis. Can existing knowledge and training in biomedical research affect the choice?
Buzzetti R, Galici V, Cirilli N, Majo F, Graziano L, Costa S, Bonacina S, Carrubba M, Davì G, Gagliano S, Cazzarolli C, Ficili F, Alghisi F, Samaja M, Magazzù G; CF Italian Patient Centered Outcomes Research Working Group (IPaCOR). Buzzetti R, et al. Among authors: alghisi f. J Cyst Fibros. 2019 May;18(3):378-381. doi: 10.1016/j.jcf.2018.02.009. Epub 2018 Mar 16. J Cyst Fibros. 2019. PMID: 29551462 Free article.
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis.
Sofia VM, Surace C, Terlizzi V, Da Sacco L, Alghisi F, Angiolillo A, Braggion C, Cirilli N, Colombo C, Di Lullo A, Padoan R, Quattrucci S, Raia V, Tuccio G, Zarrilli F, Tomaiuolo AC, Novelli A, Lucidi V, Lucarelli M, Castaldo G, Angioni A. Sofia VM, et al. Among authors: alghisi f. Mol Med. 2018 Jul 27;24(1):38. doi: 10.1186/s10020-018-0041-6. Mol Med. 2018. PMID: 30134826 Free PMC article.
Ursodeoxycholic acid and liver disease associated with cystic fibrosis: A multicenter cohort study.
Colombo C, Alicandro G, Oliver M, Lewindon PJ, Ramm GA, Ooi CY, Alghisi F, Kashirskaya N, Kondratyeva E, Corti F, Padoan R, Asherova I, Evans H, de Monestrol I, Strandvik B, Lindblad A; CF UDCA study group. Colombo C, et al. Among authors: alghisi f. J Cyst Fibros. 2022 Mar;21(2):220-226. doi: 10.1016/j.jcf.2021.03.014. Epub 2021 Apr 2. J Cyst Fibros. 2022. PMID: 33814323 Free article.
47 results