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Page 1
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
Neri M, Rossi R, Trabanelli C, Mauro A, Selvatici R, Falzarano MS, Spedicato N, Margutti A, Rimessi P, Fortunato F, Fabris M, Gualandi F, Comi G, Tedeschi S, Seia M, Fiorillo C, Traverso M, Bruno C, Giardina E, Piemontese MR, Merla G, Cau M, Marica M, Scuderi C, Borgione E, Tessa A, Astrea G, Santorelli FM, Merlini L, Mora M, Bernasconi P, Gibertini S, Sansone V, Mongini T, Berardinelli A, Pini A, Liguori R, Filosto M, Messina S, Vita G, Toscano A, Vita G, Pane M, Servidei S, Pegoraro E, Bello L, Travaglini L, Bertini E, D'Amico A, Ergoli M, Politano L, Torella A, Nigro V, Mercuri E, Ferlini A. Neri M, et al. Among authors: astrea g. Front Genet. 2020 Mar 3;11:131. doi: 10.3389/fgene.2020.00131. eCollection 2020. Front Genet. 2020. PMID: 32194622 Free PMC article.
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.
Fiorillo C, Astrea G, Savarese M, Cassandrini D, Brisca G, Trucco F, Pedemonte M, Trovato R, Ruggiero L, Vercelli L, D'Amico A, Tasca G, Pane M, Fanin M, Bello L, Broda P, Musumeci O, Rodolico C, Messina S, Vita GL, Sframeli M, Gibertini S, Morandi L, Mora M, Maggi L, Petrucci A, Massa R, Grandis M, Toscano A, Pegoraro E, Mercuri E, Bertini E, Mongini T, Santoro L, Nigro V, Minetti C, Santorelli FM, Bruno C; Italian Network on Congenital Myopathies. Fiorillo C, et al. Among authors: astrea g. Orphanet J Rare Dis. 2016 Jul 7;11(1):91. doi: 10.1186/s13023-016-0476-1. Orphanet J Rare Dis. 2016. PMID: 27387980 Free PMC article.
Reliability of the North Star Ambulatory Assessment in a multicentric setting.
Mazzone ES, Messina S, Vasco G, Main M, Eagle M, D'Amico A, Doglio L, Politano L, Cavallaro F, Frosini S, Bello L, Magri F, Corlatti A, Zucchini E, Brancalion B, Rossi F, Ferretti M, Motta MG, Cecio MR, Berardinelli A, Alfieri P, Mongini T, Pini A, Astrea G, Battini R, Comi G, Pegoraro E, Morandi L, Pane M, Angelini C, Bruno C, Villanova M, Vita G, Donati MA, Bertini E, Mercuri E. Mazzone ES, et al. Among authors: astrea g. Neuromuscul Disord. 2009 Jul;19(7):458-61. doi: 10.1016/j.nmd.2009.06.368. Epub 2009 Jun 23. Neuromuscul Disord. 2009. PMID: 19553120 Clinical Trial.
Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions.
Battini R, Chieffo D, Bulgheroni S, Piccini G, Pecini C, Lucibello S, Lenzi S, Moriconi F, Pane M, Astrea G, Baranello G, Alfieri P, Vicari S, Riva D, Cioni G, Mercuri E. Battini R, et al. Among authors: astrea g. Neuromuscul Disord. 2018 Feb;28(2):122-128. doi: 10.1016/j.nmd.2017.11.018. Epub 2017 Dec 6. Neuromuscul Disord. 2018. PMID: 29305139
Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairment.
Battini R, Lenzi S, Lucibello S, Chieffo D, Moriconi F, Cristofani P, Bulgheroni S, Cumbo F, Pane M, Baranello G, Alfieri P, Astrea G, Cioni G, Vicari S, Mercuri E. Battini R, et al. Among authors: astrea g. Neuromuscul Disord. 2021 Apr;31(4):319-327. doi: 10.1016/j.nmd.2021.01.011. Epub 2021 Feb 4. Neuromuscul Disord. 2021. PMID: 33658162
Muscle MRI in FHL1-linked reducing body myopathy.
Astrea G, Schessl J, Clement E, Tosetti M, Mercuri E, Rutherford M, Cioni G, Bönnemann CG, Muntoni F, Battini R. Astrea G, et al. Neuromuscul Disord. 2009 Oct;19(10):689-91. doi: 10.1016/j.nmd.2009.06.372. Epub 2009 Jul 17. Neuromuscul Disord. 2009. PMID: 19616434
Muscle MRI in TRPV4-related congenital distal SMA.
Astrea G, Brisca G, Fiorillo C, Valle M, Tosetti M, Bruno C, Santorelli FM, Battini R. Astrea G, et al. Neurology. 2012 Jan 31;78(5):364-5. doi: 10.1212/WNL.0b013e318245295a. Neurology. 2012. PMID: 22291064 No abstract available.
Small Complex Rearrangement in HINT1-Related Axonal Neuropathy.
Tessa A, Schifino M, Salvo E, Trovato R, Cesana L, Frosini S, Pasquariello R, Sgherri G, Battini R, Bonaglia MC, Santorelli FM, Astrea G. Tessa A, et al. Among authors: astrea g. Genes (Basel). 2024 Nov 19;15(11):1483. doi: 10.3390/genes15111483. Genes (Basel). 2024. PMID: 39596683 Free PMC article.
80 results