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

Year Number of Results
1984 1
1988 4
1989 5
1991 3
1992 1
1993 1
1997 2
1998 1
1999 1
2000 1
2001 2
2002 2
2003 2
2005 2
2006 1
2007 1
2008 2
2009 4
2010 1
2011 2
2012 2
2014 3
2015 2
2016 4
2017 4
2018 3
2019 2
2020 3
2021 2
2022 2
2023 1
2024 0

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63 results

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Page 1
Emerging genetic therapies to treat Duchenne muscular dystrophy.
Nelson SF, Crosbie RH, Miceli MC, Spencer MJ. Nelson SF, et al. Among authors: miceli mc. Curr Opin Neurol. 2009 Oct;22(5):532-8. doi: 10.1097/WCO.0b013e32832fd487. Curr Opin Neurol. 2009. PMID: 19745732 Free PMC article. Review.
Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin.
Bishop DP, Westerhausen MT, Barthelemy F, Lockwood T, Cole N, Gibbs EM, Crosbie RH, Nelson SF, Miceli MC, Doble PA, Wanagat J. Bishop DP, et al. Among authors: miceli mc. Sci Rep. 2021 Jan 13;11(1):1128. doi: 10.1038/s41598-020-80495-8. Sci Rep. 2021. PMID: 33441839 Free PMC article.
FDA Approval of Eteplirsen for Muscular Dystrophy.
Nelson SF, Miceli MC. Nelson SF, et al. Among authors: miceli mc. JAMA. 2017 Apr 11;317(14):1480. doi: 10.1001/jama.2017.2601. JAMA. 2017. PMID: 28399245 No abstract available.
63 results