Bugiardini E - Search Results

1

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.

Cardani R, Giagnacovo M, Botta A, Rinaldi F, Morgante A, Udd B, Raheem O, Penttilä S, Suominen T, Renna LV, Sansone V, Bugiardini E, Novelli G, Meola G. Cardani R, et al. Among authors: bugiardini e. J Neurol. 2012 Oct;259(10):2090-9. doi: 10.1007/s00415-012-6462-1. Epub 2012 Mar 10. J Neurol. 2012. PMID: 22407275

2

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.

3

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.

4

Vitamin D, parathyroid hormone and muscle impairment in myotonic dystrophies.

Passeri E, Bugiardini E, Sansone VA, Valaperta R, Costa E, Ambrosi B, Meola G, Corbetta S. Passeri E, et al. Among authors: bugiardini e. J Neurol Sci. 2013 Aug 15;331(1-2):132-5. doi: 10.1016/j.jns.2013.06.008. Epub 2013 Jun 25. J Neurol Sci. 2013. PMID: 23809192

5

Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2.

Cardani R, Bugiardini E, Renna LV, Rossi G, Colombo G, Valaperta R, Novelli G, Botta A, Meola G. Cardani R, et al. Among authors: bugiardini e. PLoS One. 2013 Dec 20;8(12):e83777. doi: 10.1371/journal.pone.0083777. eCollection 2013. PLoS One. 2013. PMID: 24376746 Free PMC article.

6

Consensus on cerebral involvement in myotonic dystrophy: workshop report: May 24-27, 2013, Ferrere (AT), Italy.

Bugiardini E, Meola G; DM-CNS Group. Bugiardini E, et al. Neuromuscul Disord. 2014 May;24(5):445-52. doi: 10.1016/j.nmd.2014.01.013. Epub 2014 Feb 7. Neuromuscul Disord. 2014. PMID: 24613228 No abstract available.

7

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.

8

Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2.

Perfetti A, Greco S, Fasanaro P, Bugiardini E, Cardani R, Garcia-Manteiga JM, Riba M, Cittaro D, Stupka E, Meola G, Martelli F. Perfetti A, et al. Among authors: bugiardini e. PLoS One. 2014 Apr 10;9(4):e93983. doi: 10.1371/journal.pone.0093983. eCollection 2014. PLoS One. 2014. PMID: 24722564 Free PMC article.

9

Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2.

Cardani R, Giagnacovo M, Rossi G, Renna LV, Bugiardini E, Pizzamiglio C, Botta A, Meola G. Cardani R, et al. Among authors: bugiardini e. Neuromuscul Disord. 2014 Dec;24(12):1042-53. doi: 10.1016/j.nmd.2014.06.435. Epub 2014 Jun 25. Neuromuscul Disord. 2014. PMID: 25139674

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

70 results

Search Page