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

Year Number of Results
1986 2
1987 4
1988 5
1989 5
1990 5
1991 6
1992 13
1993 14
1994 14
1995 12
1996 5
1997 7
1998 6
1999 4
2000 10
2001 10
2002 23
2003 20
2004 7
2005 12
2006 23
2007 26
2008 33
2009 31
2010 24
2011 27
2012 21
2013 18
2014 23
2015 32
2016 30
2017 20
2018 21
2019 28
2020 28
2021 21
2022 16
2023 16
2024 7

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PubMed (RefSeq) for id: 2217391253

563 results

Results by year

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Page 1
[Analysis of DMD gene variants in a single center].
Hua CX, Liu LN, Yang SZ, Xin SW, Kong XD. Hua CX, et al. Zhonghua Er Ke Za Zhi. 2024 Feb 2;62(2):153-158. doi: 10.3760/cma.j.cn112140-20230803-00072. Zhonghua Er Ke Za Zhi. 2024. PMID: 38264815 Chinese.
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity.
Kekou K, Svingou M, Vogiatzakis N, Nitsa E, Veltra D, Marinakis NM, Tilemis FN, Tzetis M, Mitrakos A, Tsaroucha C, Selenti N, Papadimas GK, Papadopoulos C, Traeger-Synodinos J, Lochmuller H, Sofocleous C. Kekou K, et al. Expert Rev Mol Diagn. 2023 Jul-Dec;23(11):999-1010. doi: 10.1080/14737159.2023.2264181. Epub 2023 Oct 24. Expert Rev Mol Diagn. 2023. PMID: 37754746
Death after High-Dose rAAV9 Gene Therapy in a Patient with Duchenne's Muscular Dystrophy.
Lek A, Wong B, Keeler A, Blackwood M, Ma K, Huang S, Sylvia K, Batista AR, Artinian R, Kokoski D, Parajuli S, Putra J, Carreon CK, Lidov H, Woodman K, Pajusalu S, Spinazzola JM, Gallagher T, LaRovere J, Balderson D, Black L, Sutton K, Horgan R, Lek M, Flotte T. Lek A, et al. N Engl J Med. 2023 Sep 28;389(13):1203-1210. doi: 10.1056/NEJMoa2307798. N Engl J Med. 2023. PMID: 37754285
563 results