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

Year Number of Results
1994 1
1999 5
2000 1
2001 3
2002 3
2003 4
2004 6
2005 1
2006 2
2007 3
2008 2
2009 1
2010 1
2011 6
2012 2
2013 7
2014 5
2015 11
2016 9
2017 5
2018 6
2019 8
2020 11
2021 4
2022 2
2023 1
2024 0

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Similar articles for PMID: 24689076

93 results

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Page 1
Nemaline myopathy caused byTNNT1 mutations in a Dutch pedigree.
van der Pol WL, Leijenaar JF, Spliet WG, Lavrijsen SW, Jansen NJ, Braun KP, Mulder M, Timmers-Raaijmakers B, Ratsma K, Dooijes D, van Haelst MM. van der Pol WL, et al. Mol Genet Genomic Med. 2014 Mar;2(2):134-7. doi: 10.1002/mgg3.52. Epub 2013 Dec 12. Mol Genet Genomic Med. 2014. PMID: 24689076 Free PMC article.
Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.
Konersman CG, Freyermuth F, Winder TL, Lawlor MW, Lagier-Tourenne C, Patel SB. Konersman CG, et al. Mol Genet Genomic Med. 2017 Nov;5(6):678-691. doi: 10.1002/mgg3.325. Epub 2017 Aug 21. Mol Genet Genomic Med. 2017. PMID: 29178646 Free PMC article.
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy.
Miyatake S, Mitsuhashi S, Hayashi YK, Purevjav E, Nishikawa A, Koshimizu E, Suzuki M, Yatabe K, Tanaka Y, Ogata K, Kuru S, Shiina M, Tsurusaki Y, Nakashima M, Mizuguchi T, Miyake N, Saitsu H, Ogata K, Kawai M, Towbin J, Nonaka I, Nishino I, Matsumoto N. Miyatake S, et al. Am J Hum Genet. 2017 Jan 5;100(1):169-178. doi: 10.1016/j.ajhg.2016.11.017. Epub 2016 Dec 22. Am J Hum Genet. 2017. PMID: 28017374 Free PMC article.
TNNT1 myopathy with novel compound heterozygous mutations.
Lee S, Eum J, Park S, Ki S, Hwang BJ, Kee Y, Chae JH. Lee S, et al. Neuromuscul Disord. 2022 Feb;32(2):176-184. doi: 10.1016/j.nmd.2021.12.003. Epub 2021 Dec 16. Neuromuscul Disord. 2022. PMID: 35165004
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.
93 results