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

Year Number of Results
1989 2
1991 1
1997 2
1998 2
1999 1
2000 1
2002 4
2003 1
2004 4
2005 7
2006 2
2007 1
2008 2
2009 2
2010 5
2011 9
2012 4
2013 4
2014 2
2015 5
2016 4
2017 1
2018 4
2019 12
2020 5
2021 9
2022 1
2023 2
2024 0

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91 results

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Page 1
[Peripapillary choroidal varix].
Nham M, Defoort-Dhellemmes S, Marks C, Smirnov VM. Nham M, et al. Among authors: defoort dhellemmes s. J Fr Ophtalmol. 2021 Oct;44(8):e483-e485. doi: 10.1016/j.jfo.2021.05.004. Epub 2021 Sep 2. J Fr Ophtalmol. 2021. PMID: 34482964 French. No abstract available.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Among authors: defoort dhellemmes s. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
[Quadruple sectoranopia].
Denion E, Defoort-Dhellemmes S, Arndt CF, Hache JC. Denion E, et al. Among authors: defoort dhellemmes s. J Fr Ophtalmol. 2005 Dec;28(10):1137-44. doi: 10.1016/s0181-5512(05)81153-2. J Fr Ophtalmol. 2005. PMID: 16395210 Review. French.
Characterization of SSBP1-related optic atrophy and foveopathy.
Meunier I, Bocquet B, Defoort-Dhellemmes S, Smirnov V, Arndt C, Picot MC, Dollfus H, Charif M, Audo I, Huguet H, Zanlonghi X, Lenaers G. Meunier I, et al. Among authors: defoort dhellemmes s. Sci Rep. 2021 Sep 21;11(1):18703. doi: 10.1038/s41598-021-98150-1. Sci Rep. 2021. PMID: 34548540 Free PMC article.
[Atrophic tamoxifen maculopathy].
Hui-Bon-Hoa AA, Defoort-Dhellemmes S, Tran TH. Hui-Bon-Hoa AA, et al. Among authors: defoort dhellemmes s. J Fr Ophtalmol. 2011 Jan;34(1):35.e1-5. doi: 10.1016/j.jfo.2010.09.017. Epub 2010 Nov 26. J Fr Ophtalmol. 2011. PMID: 21112124 French.
[Hereditary optic neuropathies: from clinical signs to diagnosis].
Meunier I, Lenaers G, Hamel C, Defoort-Dhellemmes S. Meunier I, et al. Among authors: defoort dhellemmes s. J Fr Ophtalmol. 2013 Dec;36(10):886-900. doi: 10.1016/j.jfo.2013.05.007. Epub 2013 Oct 23. J Fr Ophtalmol. 2013. PMID: 24161764 Review. French.
[Heimann-Bielschowsky phenomenon in a child: Case report].
Béal L, Defoort Dhellemmes S, Smirnov V. Béal L, et al. Among authors: defoort dhellemmes s. J Fr Ophtalmol. 2020 Nov;43(9):e311-e315. doi: 10.1016/j.jfo.2020.01.016. Epub 2020 Aug 17. J Fr Ophtalmol. 2020. PMID: 32819736 French. No abstract available.
Sensorineural hearing loss in OPA1-linked disorders.
Leruez S, Milea D, Defoort-Dhellemmes S, Colin E, Crochet M, Procaccio V, Ferré M, Lamblin J, Drouin V, Vincent-Delorme C, Lenaers G, Hamel C, Blanchet C, Juul G, Larsen M, Verny C, Reynier P, Amati-Bonneau P, Bonneau D. Leruez S, et al. Among authors: defoort dhellemmes s. Brain. 2013 Jul;136(Pt 7):e236. doi: 10.1093/brain/aws340. Epub 2013 Feb 4. Brain. 2013. PMID: 23384603 Free article. No abstract available.
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1-Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort.
Geada S, Teixeira-Marques F, Teixeira B, Carvalho AL, Lousan N, Saraiva J, Murta J, Silva R, Zanlonghi X, Defoort-Dhellemmes S, Smirnov V, Dhaenens CM, Blanchet C, Meunier I, Marques JP. Geada S, et al. Among authors: defoort dhellemmes s. Genes (Basel). 2023 Mar 30;14(4):830. doi: 10.3390/genes14040830. Genes (Basel). 2023. PMID: 37107588 Free PMC article.
91 results