Researcher
Julie De Zaeytijd
- Disciplines:Ophthalmology and optometry, Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Head and Skin (Department)
Member
From1 Oct 2018 → 25 Sep 2022 - Department of Ophthalmology (Department)
Member
From18 Feb 2016 → 30 Sep 2018
Publications
41 - 50 of 63
- Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis
Authors: Basamat Almoallem Mohammed H, Gavin Arno, Julie De Zaeytijd, Sarah Hull, Martina Suzani, Thomy JL de Ravel, Andrew Webster, Tony Moore
Number of pages: 1 - Atypical clinical and novel radiological findings in Susac syndrome : experience from a large monocentric cohort
Authors: Cathérine Dekeyser, Alexander Vanhoorne, Dimitri Hemelsoet, Liesbeth Van Hijfte, Julie De Zaeytijd, Veroniek Van Driessche, Helen Van Hoecke, Tineke Van Vrekhem, Guy Laureys
- X-linked Retinoschisis : novel clinical observations and genetic spectrum in 340 patients
Authors: Leo C. Hahn, Mary J. van Schooneveld, Nieneke L. Wesseling, Ralph J. Florijn, Jacoline B. ten Brink, Birgit I. Lissenberg-Witte, Ine Strubbe, Magda A. Meester-Smoor, Alberta A. Thiadens, Roselie M. Diederen, et al.
Pages: 191 - 202 - Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect
Authors: Artur V. Cideciyan, Samuel G. Jacobson, Arlene V. Drack, Allen C. Ho, Jason Charng, Alexandra V. Garafalo, Alejandro J. Roman, Alexander Sumaroka, Ian C. Han, Maria D. Hochstedler, et al.
Pages: 225 - 228 - Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10 : a phase 1b/2 trial
Authors: Stephen R. Russell, Arlene V. Drack, Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Alina V. Dumitrescu, Ian C. Han, Mitchell Martin, Wanda L. Pfeifer, Elliott H. Sohn, et al.
Pages: 1014 - 1021 - Clinical characterization of 66 patients with congenital retinal disease due to the deep-intronic c.2991+1655A>G mutation in CEP290
Authors: Dyon Valkenburg, Birgit Lorenz, Mies M van Genderen, Mette Bertelsen, Jan-Willem R Pott, Julie De Zaeytijd, Alberta AHJ Thiadens, Caroline CW Klaver, Hester Y Kroes, Mary J van Schooneveld, et al.
Pages: 4384 - 4391 - Visual prognosis in USH2A-associated retinitis pigmentosa is worse for patients with Usher syndrome type IIa than for those with nonsyndromic retinitis pigmentosa
Authors: Laurence HM Pierrache, Bas P Hartel, Erwin van Wijk, Magda A Meester-Smoor, Frans PM Cremers, Julie De Zaeytijd, Mary J van Schooneveld, Cor WRJ Cremers, Gislin Dagnelie, Carel B Hoyng, et al.
Pages: 1151 - 1160 - Bilateral non-arteritic ischemic optic neuropathy in a transsexual woman using excessive estrogen dosage
Authors: Katrien Wierckx, Julie De Zaeytijd, Els Elaut, GUNTER HEYLENS, Guy T'Sjoen
Pages: 407 - 409 - Exome sequencing identifies a novel RP1 mutation in a Belgian family with autosomal dominant retinitis pigmentosa
Authors: Sarah De Jaegere, Julie De Zaeytijd
Number of pages: 1 - New variants and in silico analyses in GRK1 associated Oguchi disease
Authors: James A. Poulter, Molly S. C. Gravett, Rachel L. Taylor, Kaoru Fujinami, Julie De Zaeytijd, James Bellingham, Atta Ur Rehman, Takaaki Hayashi, Mineo Kondo, Abdur Rehman, et al.
Pages: 164 - 176