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

Year Number of Results
1965 1
1966 1
1989 1
1990 1
1992 2
1993 1
1994 1
1999 1
2000 1
2003 1
2005 1
2013 1
2014 1
2017 1
2018 1
2020 2
2021 2
2022 3
2024 0

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PubMed (cited) for id: 191041

20 results

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Page 1
Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene.
Martín-Jiménez P, Fuenmayor-Fernández de la Hoz CP, Hernández-Laín A, Arteche-López A, Quesada-Espinosa JF, Voth AH, Vesperinas A, Olivé M, Domínguez-González C. Martín-Jiménez P, et al. Muscle Nerve. 2022 Oct;66(4):E13-E15. doi: 10.1002/mus.27678. Epub 2022 Jul 27. Muscle Nerve. 2022. PMID: 35833674 No abstract available.
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.
Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.
Pellerin D, Aykanat A, Ellezam B, Troiano EC, Karamchandani J, Dicaire MJ, Petitclerc M, Robertson R, Allard-Chamard X, Brunet D, Konersman CG, Mathieu J, Warman Chardon J, Gupta VA, Beggs AH, Brais B, Chrestian N. Pellerin D, et al. Ann Neurol. 2020 Apr;87(4):568-583. doi: 10.1002/ana.25685. Epub 2020 Feb 8. Ann Neurol. 2020. PMID: 31970803 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.
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.
HEREDITARY OCCURRENCE OF NEMALINE MYOPATHY.
SPIRO AJ, KENNEDY C. SPIRO AJ, et al. Arch Neurol. 1965 Aug;13:155-9. doi: 10.1001/archneur.1965.00470020045006. Arch Neurol. 1965. PMID: 14315666 No abstract available.
20 results