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CMR-verified interstitial myocardial fibrosis as a marker of subclinical cardiac involvement in LMNA mutation carriers.
Fontana M, Barison A, Botto N, Panchetti L, Ricci G, Milanesi M, Poletti R, Positano V, Siciliano G, Passino C, Lombardi M, Emdin M, Masci PG. Fontana M, et al. Among authors: barison a. JACC Cardiovasc Imaging. 2013 Jan;6(1):124-6. doi: 10.1016/j.jcmg.2012.06.013. JACC Cardiovasc Imaging. 2013. PMID: 23328570 Free article. No abstract available.
Autonomic, functional, skeletal muscle, and cardiac abnormalities are associated with increased ergoreflex sensitivity in mitochondrial disease.
Giannoni A, Aimo A, Mancuso M, Piepoli MF, Orsucci D, Aquaro GD, Barison A, De Marchi D, Taddei C, Cameli M, Raglianti V, Siciliano G, Passino C, Emdin M. Giannoni A, et al. Among authors: barison a. Eur J Heart Fail. 2017 Dec;19(12):1701-1709. doi: 10.1002/ejhf.782. Epub 2017 Feb 24. Eur J Heart Fail. 2017. PMID: 28233467 Free article.
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: barison a. 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
Cardiac magnetic resonance in patients with muscular dystrophies.
Grigoratos C, Aimo A, Barison A, Castiglione V, Todiere G, Ricci G, Siciliano G, Emdin M. Grigoratos C, et al. Among authors: barison a. Eur J Prev Cardiol. 2021 Dec 20;28(14):1526-1535. doi: 10.1177/2047487320923052. Eur J Prev Cardiol. 2021. PMID: 32418485 Review.
Cardiac magnetic resonance findings and prognosis in type 1 myotonic dystrophy.
Leali M, Aimo A, Ricci G, Torri F, Todiere G, Vergaro G, Grigoratos C, Giannoni A, Aquaro GD, Siciliano G, Emdin M, Passino C, Barison A. Leali M, et al. Among authors: barison a. J Cardiovasc Med (Hagerstown). 2023 Jun 1;24(6):340-347. doi: 10.2459/JCM.0000000000001476. Epub 2023 Apr 27. J Cardiovasc Med (Hagerstown). 2023. PMID: 37129928
Partial Lipodystrophy and LMNA p.R545H Variant.
Magno S, Ceccarini G, Barison A, Fabiani I, Giacomina A, Gilio D, Pelosini C, Rubegni A, Emdin M, Gatti GL, Santorelli FM, Sessa MR, Santini F. Magno S, et al. Among authors: barison a. J Clin Med. 2021 Mar 9;10(5):1142. doi: 10.3390/jcm10051142. J Clin Med. 2021. PMID: 33803191 Free PMC article.
Atypical Progeroid Syndrome and Partial Lipodystrophy Due to LMNA Gene p.R349W Mutation.
Magno S, Ceccarini G, Pelosini C, Ferrari F, Prodam F, Gilio D, Maffei M, Sessa MR, Barison A, Ciccarone A, Emdin M, Aimaretti G, Santini F. Magno S, et al. Among authors: barison a. J Endocr Soc. 2020 Aug 1;4(10):bvaa108. doi: 10.1210/jendso/bvaa108. eCollection 2020 Oct 1. J Endocr Soc. 2020. PMID: 32913962 Free PMC article.
Late gadolinium enhancement role in arrhythmic risk stratification of patients with LMNA cardiomyopathy: results from a long-term follow-up multicentre study.
Peretto G, Barison A, Forleo C, Di Resta C, Esposito A, Aquaro GD, Scardapane A, Palmisano A, Emdin M, Resta N, Santoni A, Guaricci AI, Santobuono VE, Pepe M, Favale S, Ferrari M, Benedetti S, Della Bella P, Sala S. Peretto G, et al. Among authors: barison a. Europace. 2020 Dec 23;22(12):1864-1872. doi: 10.1093/europace/euaa171. Europace. 2020. PMID: 32995851
278 results