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

Year Number of Results
2002 3
2004 1
2005 3
2006 1
2007 2
2009 5
2010 2
2011 1
2012 3
2013 1
2014 4
2015 2
2016 1
2017 3
2018 2
2019 8
2020 6
2021 4
2022 4
2023 5
2024 0

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PubMed (GeneRIF) for id: 375790

50 results

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Page 1
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
Jacquier A, Risson V, Simonet T, Roussange F, Lacoste N, Ribault S, Carras J, Theuriet J, Girard E, Grosjean I, Le Goff L, Kröger S, Meltoranta J, Bauché S, Sternberg D, Fournier E, Kostera-Pruszczyk A, O'Connor E, Eymard B, Lochmüller H, Martinat C, Schaeffer L. Jacquier A, et al. Acta Neuropathol. 2022 Oct;144(4):707-731. doi: 10.1007/s00401-022-02475-8. Epub 2022 Aug 10. Acta Neuropathol. 2022. PMID: 35948834 Free PMC article.
Association between frailty and C-terminal agrin fragment with 3-month mortality following ST-elevation myocardial infarction.
de Souza Ramos JTG, Ferrari FS, Andrade MF, de Melo CS, Boas PJFV, Costa NA, Pereira AG, Dorna MS, Azevedo PS, Banerjee J, Phillips BE, Atherton PJ, Polegato BF, Okoshi K, Zanati SG, Paiva SAR, Zornoff LAM, Minicucci MF. de Souza Ramos JTG, et al. Exp Gerontol. 2022 Feb;158:111658. doi: 10.1016/j.exger.2021.111658. Epub 2021 Dec 14. Exp Gerontol. 2022. PMID: 34920013
Myasthenia gravis genome-wide association study implicates AGRN as a risk locus.
Topaloudi A, Zagoriti Z, Flint AC, Martinez MB, Yang Z, Tsetsos F, Christou YP, Lagoumintzis G, Yannaki E, Zamba-Papanicolaou E, Tzartos J, Tsekmekidou X, Kotsa K, Maltezos E, Papanas N, Papazoglou D, Passadakis P, Roumeliotis A, Roumeliotis S, Theodoridis M, Thodis E, Panagoutsos S, Yovos J, Stamatoyannopoulos J, Poulas K, Kleopa K, Tzartos S, Georgitsi M, Paschou P. Topaloudi A, et al. J Med Genet. 2022 Aug;59(8):801-809. doi: 10.1136/jmedgenet-2021-107953. Epub 2021 Aug 16. J Med Genet. 2022. PMID: 34400559
50 results