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

Year Number of Results
1949 1
1953 1
1959 1
2004 1
2005 3
2006 3
2007 1
2008 2
2009 1
2010 1
2012 3
2013 5
2014 5
2015 2
2016 2
2017 4
2018 5
2019 10
2020 13
2021 4
2022 4
2023 6
2024 4

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69 results

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Page 1
[Gene therapy for retinitis pigmentosa].
Ducloyer JB, Le Meur G, Cronin T, Adjali O, Weber M. Ducloyer JB, et al. Among authors: le meur g. Med Sci (Paris). 2020 Jun-Jul;36(6-7):607-615. doi: 10.1051/medsci/2020095. Epub 2020 Jul 2. Med Sci (Paris). 2020. PMID: 32614312 Free article. Review. French.
Mannose-coupled AAV2: A second-generation AAV vector for increased retinal gene therapy efficiency.
Mével M, Pichard V, Bouzelha M, Alvarez-Dorta D, Lalys PA, Provost N, Allais M, Mendes A, Landagaray E, Ducloyer JB, Toublanc E, Galy A, Brument N, Lefevre GM, Gouin SG, Isiegas C, Le Meur G, Cronin T, Le Guiner C, Weber M, Moullier P, Ayuso E, Deniaud D, Adjali O. Mével M, et al. Among authors: le meur g. Mol Ther Methods Clin Dev. 2024 Jan 17;32(1):101187. doi: 10.1016/j.omtm.2024.101187. eCollection 2024 Mar 14. Mol Ther Methods Clin Dev. 2024. PMID: 38327809 Free PMC article.
[Impact of prematurity on the optic nerve].
Bielefeld V, Rousseau J, Denis C, Giraud L, Vallon A, Huet K, Lehuede K, Konig R, Lassalle D, Wendel J, Péré M, Plaineau M, Ducloyer JB, Couret C, Lebranchu P, Le Meur G. Bielefeld V, et al. Among authors: le meur g. J Fr Ophtalmol. 2021 May;44(5):703-710. doi: 10.1016/j.jfo.2020.06.048. Epub 2021 Apr 8. J Fr Ophtalmol. 2021. PMID: 33840493 French.
[Bilateral optic nerve infiltration by carcinomatous meningitis].
Bielefeld V, Assad S, Guguen C, Goupil F, Le Meur G, Lebranchu P, Laballe R. Bielefeld V, et al. Among authors: le meur g. J Fr Ophtalmol. 2020 May;43(5):444-445. doi: 10.1016/j.jfo.2019.09.021. Epub 2020 Mar 31. J Fr Ophtalmol. 2020. PMID: 32245580 French. No abstract available.
Evaluation of a machine-learning model based on laboratory parameters for the prediction of acute leukaemia subtypes: a multicentre model development and validation study in France.
Alcazer V, Le Meur G, Roccon M, Barriere S, Le Calvez B, Badaoui B, Spaeth A, Kosmider O, Freynet N, Eveillard M, Croizier C, Chevalier S, Sujobert P. Alcazer V, et al. Among authors: le meur g. Lancet Digit Health. 2024 May;6(5):e323-e333. doi: 10.1016/S2589-7500(24)00044-X. Lancet Digit Health. 2024. PMID: 38670741 Free article.
Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A.
Marchesin V, Pérez-Martí A, Le Meur G, Pichler R, Grand K, Klootwijk ED, Kesselheim A, Kleta R, Lienkamp S, Simons M. Marchesin V, et al. Among authors: le meur g. Cell Rep. 2019 Dec 24;29(13):4407-4421.e5. doi: 10.1016/j.celrep.2019.11.066. Cell Rep. 2019. PMID: 31875549 Free PMC article.
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Chesneau B, Aubert-Mucca M, Fremont F, Pechmeja J, Soler V, Isidor B, Nizon M, Dollfus H, Kaplan J, Fares-Taie L, Rozet JM, Busa T, Lacombe D, Naudion S, Amiel J, Rio M, Attie-Bitach T, Lesage C, Thouvenin D, Odent S, Morel G, Vincent-Delorme C, Boute O, Vanlerberghe C, Dieux A, Boussion S, Faivre L, Pinson L, Laffargue F, Le Guyader G, Le Meur G, Prieur F, Lambert V, Laudier B, Cottereau E, Ayuso C, Corton-Pérez M, Bouneau L, Le Caignec C, Gaston V, Jeanton-Scaramouche C, Dupin-Deguine D, Calvas P, Chassaing N, Plaisancié J. Chesneau B, et al. Among authors: le meur g. Clin Genet. 2022 May;101(5-6):494-506. doi: 10.1111/cge.14123. Epub 2022 Feb 27. Clin Genet. 2022. PMID: 35170016 Free article.
69 results