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Cell environment shapes TDP-43 function with implications in neuronal and muscle disease.
Šušnjar U, Škrabar N, Brown AL, Abbassi Y, Phatnani H; NYGC ALS Consortium; Cortese A, Cereda C, Bugiardini E, Cardani R, Meola G, Ripolone M, Moggio M, Romano M, Secrier M, Fratta P, Buratti E. Šušnjar U, et al. Among authors: bugiardini e. Commun Biol. 2022 Apr 5;5(1):314. doi: 10.1038/s42003-022-03253-8. Commun Biol. 2022. PMID: 35383280 Free PMC article.
Muscle biopsy.
Meola G, Bugiardini E, Cardani R. Meola G, et al. Among authors: bugiardini e. J Neurol. 2012 Apr;259(4):601-10. doi: 10.1007/s00415-011-6193-8. Epub 2011 Jul 30. J Neurol. 2012. PMID: 21805256 Review.
Plasma microRNAs as biomarkers for myotonic dystrophy type 1.
Perfetti A, Greco S, Bugiardini E, Cardani R, Gaia P, Gaetano C, Meola G, Martelli F. Perfetti A, et al. Among authors: bugiardini e. Neuromuscul Disord. 2014 Jun;24(6):509-15. doi: 10.1016/j.nmd.2014.02.005. Epub 2014 Feb 18. Neuromuscul Disord. 2014. PMID: 24679513 Free article.
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype.
Bugiardini E, Rivolta I, Binda A, Soriano Caminero A, Cirillo F, Cinti A, Giovannoni R, Botta A, Cardani R, Wicklund MP, Meola G. Bugiardini E, et al. Neuromuscul Disord. 2015 Apr;25(4):301-7. doi: 10.1016/j.nmd.2015.01.006. Epub 2015 Jan 21. Neuromuscul Disord. 2015. PMID: 25660391
GSK3β mediates muscle pathology in myotonic dystrophy.
Jones K, Wei C, Iakova P, Bugiardini E, Schneider-Gold C, Meola G, Woodgett J, Killian J, Timchenko NA, Timchenko LT. Jones K, et al. Among authors: bugiardini e. J Clin Invest. 2012 Dec;122(12):4461-72. doi: 10.1172/JCI64081. Epub 2012 Nov 19. J Clin Invest. 2012. PMID: 23160194 Free PMC article.
75 results