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Melanocortin-1 receptor (MC1R): a review for dermatologists.
Guida S, Puig S, DI Resta C, Sallustio F, Mangano E, Stabile G, Longo C, Pellacani G, Guida G, Rongioletti F. Guida S, et al. Among authors: di resta c. Ital J Dermatol Venerol. 2024 Jun;159(3):285-293. doi: 10.23736/S2784-8671.24.07839-3. Epub 2024 Feb 20. Ital J Dermatol Venerol. 2024. PMID: 38376504 Review.
Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy.
Peretto G, Di Resta C, Perversi J, Forleo C, Maggi L, Politano L, Barison A, Previtali SC, Carboni N, Brun F, Pegoraro E, D'Amico A, Rodolico C, Magri F, Manzi RC, Palladino A, Isola F, Gigli L, Mongini TE, Semplicini C, Calore C, Ricci G, Comi GP, Ruggiero L, Bertini E, Bonomo P, Nigro G, Resta N, Emdin M, Favale S, Siciliano G, Santoro L, Sinagra G, Limongelli G, Ambrosi A, Ferrari M, Golzio PG, Bella PD, Benedetti S, Sala S; Italian Network for Laminopathies (NIL). Peretto G, et al. Among authors: resta n, di resta c. Ann Intern Med. 2019 Oct 1;171(7):458-463. doi: 10.7326/M18-2768. Epub 2019 Sep 3. Ann Intern Med. 2019. PMID: 31476771
Advance in Genomics of Rare Genetic Diseases.
Sommariva E, Bellin M, Di Resta C. Sommariva E, et al. Among authors: di resta c. Biomolecules. 2023 Sep 25;13(10):1441. doi: 10.3390/biom13101441. Biomolecules. 2023. PMID: 37892123 Free PMC article.
Editorial: Whole Genome Sequencing for rare diseases.
Di Resta C, D'Argenio V. Di Resta C, et al. Front Med (Lausanne). 2023 Sep 19;10:1267930. doi: 10.3389/fmed.2023.1267930. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37795418 Free PMC article. No abstract available.
Multimodal Detection and Targeting of Biopsy-Proven Myocardial Inflammation in Genetic Cardiomyopathies: A Pilot Report.
Peretto G, De Luca G, Villatore A, Di Resta C, Sala S, Palmisano A, Vignale D, Campochiaro C, Lazzeroni D, De Gaspari M, Rizzo S, Busnardo E, Ferro P, Gianolli L, Basso C, Dagna L, Esposito A, Benedetti S, Della Bella P. Peretto G, et al. Among authors: di resta c. JACC Basic Transl Sci. 2023 Jul 5;8(7):755-765. doi: 10.1016/j.jacbts.2023.02.018. eCollection 2023 Jul. JACC Basic Transl Sci. 2023. PMID: 37547072 Free PMC article.
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells.
Salvarani N, Peretto G, Silvia C, Villatore A, Thairi C, Santoni A, Galli C, Carrera P, Sala S, Benedetti S, Di Pasquale E, Di Resta C. Salvarani N, et al. Among authors: di resta c. Int J Mol Sci. 2023 May 31;24(11):9548. doi: 10.3390/ijms24119548. Int J Mol Sci. 2023. PMID: 37298497 Free PMC article.
65 results