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Results by year

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

Year Number of Results
1987 1
1989 2
1992 2
1993 1
1994 2
1996 2
1997 1
1998 5
1999 7
2000 9
2001 6
2002 10
2003 4
2004 7
2005 6
2006 2
2007 4
2008 3
2009 3
2010 2
2011 1
2012 2
2013 7
2014 3
2015 3
2016 5
2017 2
2018 3
2019 3
2020 5
2021 3
2022 6
2023 2
2024 0

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Similar articles for PMID: 15665378

112 results

Results by year

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Page 1
Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy.
Géraud J, Dieterich K, Rendu J, Uro Coste E, Dobrzynski M, Marcorelle P, Ioos C, Romero NB, Baudou E, Brocard J, Coville AC, Fauré J, Koenig M, Juntas Morales R, Lacène E, Madelaine A, Marty I, Pegeot H, Theze C, Siegfried A, Cossee M, Cances C. Géraud J, et al. J Med Genet. 2021 Sep;58(9):602-608. doi: 10.1136/jmedgenet-2019-106714. Epub 2020 Sep 29. J Med Genet. 2021. PMID: 32994279 Free PMC article.
Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy.
Ilkovski B, Mokbel N, Lewis RA, Walker K, Nowak KJ, Domazetovska A, Laing NG, Fowler VM, North KN, Cooper ST. Ilkovski B, et al. J Neuropathol Exp Neurol. 2008 Sep;67(9):867-77. doi: 10.1097/NEN.0b013e318183a44f. J Neuropathol Exp Neurol. 2008. PMID: 18716557 Free PMC article.
112 results