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

Year Number of Results
2004 1
2009 1
2010 1
2013 5
2014 3
2015 4
2016 5
2017 4
2018 7
2019 7
2020 6
2021 13
2022 10
2023 3
2024 6

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64 results

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Page 1
Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial.
Russell SR, Drack AV, Cideciyan AV, Jacobson SG, Leroy BP, Van Cauwenbergh C, Ho AC, Dumitrescu AV, Han IC, Martin M, Pfeifer WL, Sohn EH, Walshire J, Garafalo AV, Krishnan AK, Powers CA, Sumaroka A, Roman AJ, Vanhonsebrouck E, Jones E, Nerinckx F, De Zaeytijd J, Collin RWJ, Hoyng C, Adamson P, Cheetham ME, Schwartz MR, den Hollander W, Asmus F, Platenburg G, Rodman D, Girach A. Russell SR, et al. Among authors: de zaeytijd j. Nat Med. 2022 May;28(5):1014-1021. doi: 10.1038/s41591-022-01755-w. Epub 2022 Apr 4. Nat Med. 2022. PMID: 35379979 Free PMC article. Clinical Trial.
An atypical case of neurosarcoidosis presenting with neovascular glaucoma.
Vereecken M, Hollanders K, De Bruyn D, Ninclaus V, De Zaeytijd J, De Schryver I. Vereecken M, et al. Among authors: de zaeytijd j. J Ophthalmic Inflamm Infect. 2018 Apr 18;8(1):7. doi: 10.1186/s12348-018-0149-4. J Ophthalmic Inflamm Infect. 2018. PMID: 29671151 Free PMC article. Review.
An eye-opening case report of constrictive pericarditis.
Dhont S, Van Belleghem Y, De Zaeytijd J, Vandecasteele E. Dhont S, et al. Among authors: de zaeytijd j. Eur Heart J Case Rep. 2022 Jul 25;6(7):ytac287. doi: 10.1093/ehjcr/ytac287. eCollection 2022 Jul. Eur Heart J Case Rep. 2022. PMID: 35975098 Free PMC article.
Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease.
Dueñas Rey A, Del Pozo Valero M, Bouckaert M, Wood KA, Van den Broeck F, Daich Varela M, Thomas HB, Van Heetvelde M, De Bruyne M, Van de Sompele S, Bauwens M, Lenaerts H, Mahieu Q, Josifova D; Genomics England Research Consortium; Rivolta C, O'Keefe RT, Ellingford J, Webster AR, Arno G, Ayuso C, De Zaeytijd J, Leroy BP, De Baere E, Coppieters F. Dueñas Rey A, et al. Among authors: de zaeytijd j. Genome Med. 2024 Jan 6;16(1):7. doi: 10.1186/s13073-023-01277-1. Genome Med. 2024. PMID: 38184646 Free PMC article.
Colour Vision in Stargardt Disease.
Vandenbroucke T, Buyl R, De Zaeytijd J, Bauwens M, Uvijls A, De Baere E, Leroy BP. Vandenbroucke T, et al. Among authors: de zaeytijd j. Ophthalmic Res. 2015;54(4):181-94. doi: 10.1159/000438906. Epub 2015 Oct 23. Ophthalmic Res. 2015. PMID: 26492201
Diplopia as presenting sign of Turcot syndrome.
Ninclaus VG, Walraedt S, Baert E, Laureys G, Leroy BP, De Zaeytijd J. Ninclaus VG, et al. Among authors: de zaeytijd j. Int Ophthalmol. 2017 Feb;37(1):275-278. doi: 10.1007/s10792-016-0246-z. Epub 2016 May 3. Int Ophthalmol. 2017. PMID: 27143045
X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients.
Hahn LC, van Schooneveld MJ, Wesseling NL, Florijn RJ, Ten Brink JB, Lissenberg-Witte BI, Strubbe I, Meester-Smoor MA, Thiadens AA, Diederen RM, van Cauwenbergh C, de Zaeytijd J, Walraedt S, de Baere E, Klaver CCW, Ossewaarde-van Norel J, van den Born LI, Hoyng CB, van Genderen MM, Sieving PA, Leroy BP, Bergen AA, Boon CJF. Hahn LC, et al. Among authors: de zaeytijd j. Ophthalmology. 2022 Feb;129(2):191-202. doi: 10.1016/j.ophtha.2021.09.021. Epub 2021 Oct 6. Ophthalmology. 2022. PMID: 34624300 Free article.
Optic nerve involvement in CACNA1F-related disease: observations from a multicentric case series.
Marziali E, Van Den Broeck F, Bargiacchi S, Fortunato P, Caputo R, Sodi A, De Zaeytijd J, Murro V, Mucciolo DP, Giorgio D, Passerini I, Palazzo V, Peluso F, de Baere E, Zeitz C, Leroy BP, Secci J, Bacci GM. Marziali E, et al. Among authors: de zaeytijd j. Ophthalmic Genet. 2023 Apr;44(2):152-162. doi: 10.1080/13816810.2022.2132514. Epub 2022 Dec 5. Ophthalmic Genet. 2023. PMID: 36469668
64 results