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

Year Number of Results
2003 2
2005 1
2006 1
2007 1
2009 1
2010 1
2011 3
2012 4
2013 3
2014 3
2015 2
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2017 5
2018 4
2019 6
2020 4
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2022 6
2023 4
2024 2

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Page 1
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree.
Emperador S, Habbane M, López-Gallardo E, Del Rio A, Llobet L, Mateo J, Sanz-López AM, Fernández-García MJ, Sánchez-Tocino H, Benbunan-Ferreiro S, Calabuig-Goena M, Narvaez-Palazón C, Fernández-Vega B, González-Iglesias H, Urreizti R, Artuch R, Pacheu-Grau D, Bayona-Bafaluy P, Montoya J, Ruiz-Pesini E. Emperador S, et al. Among authors: mateo j. Orphanet J Rare Dis. 2024 Apr 6;19(1):148. doi: 10.1186/s13023-024-03165-2. Orphanet J Rare Dis. 2024. PMID: 38582886 Free PMC article.
Correction to: Recovery course of foveal microstructure in the nonsurgical resolution of full-thickness macular hole.
Mansour HA, Uwaydat SH, Parodi M, Jürgens I, Smiddy W, Ellabban AA, Schwartz SG, Foster RE, Ascaso J, Leoz MS, Belotto S, Mateo J, Olivier-Pascual N, Lima LH, Navea A, Neila EMR, Castillo RA, Alaman AS, Mansour AM; Collaborators of the Nonsurgical Resolution of Macular Hole Study Group. Mansour HA, et al. Among authors: mateo j. Graefes Arch Clin Exp Ophthalmol. 2022 Oct;260(10):3403. doi: 10.1007/s00417-022-05712-8. Graefes Arch Clin Exp Ophthalmol. 2022. PMID: 35648224 Free article. No abstract available.
51 results