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Results by year

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

Year Number of Results
1975 1
1976 1
1978 2
1980 2
1982 1
1983 3
1984 2
1985 1
1986 3
1987 1
1988 1
1989 1
1990 2
1992 1
1993 3
1994 3
1995 1
1996 2
1997 2
1998 2
2000 2
2001 4
2002 1
2003 2
2004 4
2005 5
2006 3
2007 4
2008 1
2009 6
2010 7
2011 10
2012 6
2013 14
2014 8
2015 10
2016 14
2017 11
2018 10
2019 4
2020 13
2021 13
2022 7
2023 0

Text availability

Article attribute

Article type

Publication date

PubMed for id: 414119

177 results

Results by year

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Page 1
BAG3-related myofibrillar myopathy in a Chinese family.
Lee HC, Cherk SW, Chan SK, Wong S, Tong TW, Ho WS, Chan AY, Lee KC, Mak CM. Lee HC, et al. Clin Genet. 2012 Apr;81(4):394-8. doi: 10.1111/j.1399-0004.2011.01659.x. Epub 2011 Apr 4. Clin Genet. 2012. PMID: 21361913
BAG3 myofibrillar myopathy presenting with cardiomyopathy.
Konersman CG, Bordini BJ, Scharer G, Lawlor MW, Zangwill S, Southern JF, Amos L, Geddes GC, Kliegman R, Collins MP. Konersman CG, et al. Neuromuscul Disord. 2015 May;25(5):418-22. doi: 10.1016/j.nmd.2015.01.009. Epub 2015 Feb 4. Neuromuscul Disord. 2015. PMID: 25728519
Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review.
Ehsani E, Khamirani HJ, Abbasi Z, Gohari M, Zoghi S, Mohammadi S, Dianatpour M, Tabei SMB, Mohamadjani O, Dastgheib SA. Ehsani E, et al. Eur J Med Genet. 2022 Aug;65(8):104552. doi: 10.1016/j.ejmg.2022.104552. Epub 2022 Jun 22. Eur J Med Genet. 2022. PMID: 35752288 Review.
177 results