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Results by year

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

Year Number of Results
1941 2
1976 1
1977 1
1978 1
1981 1
1982 2
1984 1
1985 1
1986 1
1987 1
1989 1
1991 2
1992 1
1993 2
1994 3
1995 2
1996 2
1997 7
1998 5
1999 5
2000 3
2001 5
2002 1
2003 5
2004 7
2005 9
2006 5
2007 9
2008 8
2009 10
2010 6
2011 13
2012 14
2013 18
2014 17
2015 17
2016 15
2017 15
2018 15
2019 14
2020 13
2021 12
2022 11
2023 3
2024 0

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Similar articles for PMID: 21288719

260 results

Results by year

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Page 1
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy.
Ortolano S, Tarrío R, Blanco-Arias P, Teijeira S, Rodríguez-Trelles F, García-Murias M, Delague V, Lévy N, Fernández JM, Quintáns B, Millán BS, Carracedo A, Navarro C, Sobrido MJ. Ortolano S, et al. Neuromuscul Disord. 2011 Apr;21(4):254-62. doi: 10.1016/j.nmd.2010.12.011. Epub 2011 Feb 1. Neuromuscul Disord. 2011. PMID: 21288719
Hereditary myosin myopathies.
Oldfors A. Oldfors A. Neuromuscul Disord. 2007 May;17(5):355-67. doi: 10.1016/j.nmd.2007.02.008. Epub 2007 Apr 16. Neuromuscul Disord. 2007. PMID: 17434305 Review.
Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
Overeem S, Schelhaas HJ, Blijham PJ, Grootscholten MI, ter Laak HJ, Timmermans J, van den Wijngaard A, Zwarts MJ. Overeem S, et al. Neuromuscul Disord. 2007 Jun;17(6):490-3. doi: 10.1016/j.nmd.2007.02.007. Epub 2007 Mar 23. Neuromuscul Disord. 2007. PMID: 17383184
260 results