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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2004 1
2005 2
2008 4
2009 6
2010 6
2011 9
2012 15
2013 10
2014 13
2015 17
2016 10
2017 8
2018 16
2019 12
2020 14
2021 16
2022 12
2023 14
2024 10
2025 7
2026 2

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187 results

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Page 1
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.
Gorgoglione D, Sabbatini D, Riguzzi P, Capece G, Pane M, Servidei S, Briganti M, Sancricca C, Bruschi F, Ardissone A, Masson R, Gallone A, Maggi L, Picillo E, Politano L, Petrosino A, Vianello S, Penzo M, Villa M, Sframeli M, Allegra C, Barp A, Di Bari A, Salmin F, Albamonte E, Colacicco G, Panicucci C, Traverso M, Palermo C, Lerario A, Velardo D, D'Angelo MG, Berardinelli A, Gardani A, Nicotra R, Parravicini S, Siciliano G, Ricci G, Torri F, Gadaleta G, Urbano G, Rolle E, Ricci F, D'Amico A, Catteruccia M, Pini A, Giannotta M, Battini R, Marinella G, Previtali SC, Zambon AA, Ferlini A, Fortunato F, Magri F, Mongini TE, Sansone VA, Bruno C, Messina S, Nigro V, Moroni I, Mercuri E, Bello L, Pegoraro E. Gorgoglione D, et al. Among authors: politano l. Brain. 2025 May 13;148(5):1695-1706. doi: 10.1093/brain/awae358. Brain. 2025. PMID: 39499670 Free article.
DMD Genotypes and Motor Function in Duchenne Muscular Dystrophy: A Multi-institution Meta-analysis With Implications for Clinical Trials.
Muntoni F, Signorovitch J, Sajeev G, Lane H, Jenkins M, Dieye I, Ward SJ, McDonald C, Goemans N, Niks EH, Wong B, Servais L, Straub V, Guglieri M, de Groot IJM, Chesshyre M, Tian C, Manzur AY, Mercuri E, Aartsma-Rus A; Association Française Contre Les Myopathies; on behalf of Universitaire Ziekenhuizen Leuven Group, PRO-DMD-01, The UK NorthStar Clinical Network, CCHMC, and The DMD Italian Group. Muntoni F, et al. Neurology. 2023 Apr 11;100(15):e1540-e1554. doi: 10.1212/WNL.0000000000201626. Epub 2023 Feb 1. Neurology. 2023. PMID: 36725339 Free PMC article.
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form.
Ricci G, Torri F, Ruggiero L, Vercelli L, Gadaleta G, Rolle E, Risi B, Carraro E, Evangelista T, Bugiardini E, Dubuisson N, Voermans N, Siciliano G, Mongini T, Filosto M; Italian Clinical Network for FSHD. Ricci G, et al. Neurol Sci. 2025 Sep;46(9):4633-4643. doi: 10.1007/s10072-025-08276-7. Epub 2025 Jun 13. Neurol Sci. 2025. PMID: 40506648
Aging research from bench to bedside and beyond: What we learned from Sammy Basso.
Lattanzi G, Lanzuolo C, Cugudda E, Maggi L, Politano L, Santiago-Fernández O, Ricci G, Squarzoni S, Lopez-Otin C; Italian Network for Laminopathies. Lattanzi G, et al. Among authors: politano l. Aging Cell. 2024 Dec;23(12):e14414. doi: 10.1111/acel.14414. Aging Cell. 2024. PMID: 39663551 Free PMC article. No abstract available.
Landscape Analysis of COL6A1, COL6A2, and COL6A3 Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report.
Fortunato F, Fiocco L, Margutti A, Neri M, D'Amico A, Bertini E, Ricci E, Mercuri EM, Pane M, Massa R, Greco G, Berardinelli AL, Cereda C, Pini A, Merlini L, Fusco C, Rodolico C, Messina S, Fiorillo C, Bruno C, Pedemonte M, Traverso M, Moroni I, Maggi L, Gibertini S, Pegoraro E, Picillo E, Politano L, Scutifero M, Vercellino F, Massaro F, Filosto M, Gasparini P, Ricci F, Mongini TE, Selvatici R, Ferlini A, Gualandi F. Fortunato F, et al. Among authors: politano l. Biomolecules. 2025 Oct 8;15(10):1426. doi: 10.3390/biom15101426. Biomolecules. 2025. PMID: 41154655 Free PMC article.
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients.
Strafella C, Megalizzi D, Trastulli G, Proietti Piorgo E, Colantoni L, Tasca G, Monforte M, Zampatti S, Primiano G, Sancricca C, Bortolani S, Torchia E, Ravera B, Torri F, Gadaleta G, Risi B, Caria F, Gerardi F, Carraro E, Gioiosa V, Garibaldi M, Tufano L, Frezza E, Massa R, Caltagirone C, Pennisi EM, Petrucci A, Pane M, Frongia A, Gragnani F, Scutifero M, Mandich P, Grandis M, Maioli MA, Casali C, Manfroi E, Politano L, Passamano L, Petillo R, Rodolico C, Pugliese A, Previtali SC, Sansone V, Vercelli L, Mongini TE, Ricci G, Siciliano G, Filosto M, Ricci E, Cascella R, Giardina E; FSHD Italian Clinical Group. Strafella C, et al. Among authors: politano l. Clin Epigenetics. 2024 Oct 22;16(1):148. doi: 10.1186/s13148-024-01747-2. Clin Epigenetics. 2024. PMID: 39438900 Free PMC article.
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular Dystrophy.
Bello L, Riguzzi P, Albamonte E, Astrea G, Battini R, Barp A, Berardinelli AL, Bertini ES, Brolatti N, Bruno C, Corti S, D'Amico A, D'Angelo MG, Dallavalle G, Liguori R, Maggi L, Magri F, Mancuso M, Masson R, Mercuri E, Minetti C, Messina S, Mongini T, Musumeci O, Nigro V, Pane M, Panicucci C, Pedemonte M, Pini A, Politano L, Previtali S, Ricci F, Ricci G, Ruggiero L, Sansone V, Siciliano G, Trabacca A, Trucco F, Velardo D, Pegoraro E, Comi GP. Bello L, et al. Among authors: politano l. Drugs R D. 2025 Jun;25(2):99-106. doi: 10.1007/s40268-025-00512-x. Epub 2025 May 28. Drugs R D. 2025. PMID: 40434600 Free PMC article. Review.
187 results