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Page 1
Characterization of cardiovascular involvement in pseudoxanthoma elasticum families.
Campens L, Vanakker OM, Trachet B, Segers P, Leroy BP, De Zaeytijd J, Voet D, De Paepe A, De Backer T, De Backer J. Campens L, et al. Among authors: de paepe a, de backer t, de backer j, de zaeytijd j. Arterioscler Thromb Vasc Biol. 2013 Nov;33(11):2646-52. doi: 10.1161/ATVBAHA.113.301901. Epub 2013 Aug 22. Arterioscler Thromb Vasc Biol. 2013. PMID: 23968982
Bifocal optic and facial nerve t-cell lymphoma.
Van Hoey A, Shah A, De Zaeytijd J, Van Den Broecke C, Decock C, Leroy BP. Van Hoey A, et al. Among authors: de zaeytijd j. Bull Soc Belge Ophtalmol. 2013;(322):63-9. Bull Soc Belge Ophtalmol. 2013. PMID: 24923084
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients.
Bauwens M, De Zaeytijd J, Weisschuh N, Kohl S, Meire F, Dahan K, Depasse F, De Jaegere S, De Ravel T, De Rademaeker M, Loeys B, Coppieters F, Leroy BP, De Baere E. Bauwens M, et al. Among authors: de rademaeker m, de jaegere s, de ravel t, de baere e, de zaeytijd j. Hum Mutat. 2015 Jan;36(1):39-42. doi: 10.1002/humu.22716. Hum Mutat. 2015. PMID: 25346251
Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.
AlMoallem B, Bauwens M, Walraedt S, Delbeke P, De Zaeytijd J, Kestelyn P, Meire F, Janssens S, van Cauwenbergh C, Verdin H, Hooghe S, Kumar Thakur P, Coppieters F, De Leeneer K, Devriendt K, Leroy BP, De Baere E. AlMoallem B, et al. Among authors: de leeneer k, de baere e, de zaeytijd j. Invest Ophthalmol Vis Sci. 2015 Feb 12;56(3):1701-10. doi: 10.1167/iovs.14-15938. Invest Ophthalmol Vis Sci. 2015. PMID: 25678693
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 baere e, de zaeytijd j. Ophthalmic Res. 2015;54(4):181-94. doi: 10.1159/000438906. Epub 2015 Oct 23. Ophthalmic Res. 2015. PMID: 26492201
Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa.
Pierrache LH, Hartel BP, van Wijk E, Meester-Smoor MA, Cremers FP, de Baere E, de Zaeytijd J, van Schooneveld MJ, Cremers CW, Dagnelie G, Hoyng CB, Bergen AA, Leroy BP, Pennings RJ, van den Born LI, Klaver CC. Pierrache LH, et al. Among authors: de baere e, de zaeytijd j. Ophthalmology. 2016 May;123(5):1151-60. doi: 10.1016/j.ophtha.2016.01.021. Epub 2016 Feb 27. Ophthalmology. 2016. PMID: 26927203
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