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Filip Van Den Broeck

Showing results (1-10 of 18) with videos related to

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Stem Cell Research|November 6, 2025
Generation and characterization of three human induced pluripotent stem cell lines (UGENTi005, UGENTi006 and UGENTi007) from patients with autosomal dominant adult-onset maculopathy due to RPE65 variant c.1555G>A, p.(E519K)Eline Van Vooren, Filip Van den Broeck, Esperanza Daal, et al.
Investigative Ophthalmology & Visual Science|April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt DiseaseJeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Frontiers in Medicine|August 21, 2023
Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital ExperienceHwei Wuen Chan, Filip Van den Broeck, Axelle Cools, et al.
Surgical Innovation|January 23, 2019
Articulated Instruments and 3D Visualization: A Synergy? Evaluation of Execution Time, Errors, and Visual FatigueFrank Dewaele, Tim De Pauw, Nicolaas Lumen, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
Ophthalmic Genetics|December 5, 2022
Optic nerve involvement in <i>CACNA1F</i>-related disease: observations from a multicentric case seriesElisa Marziali, Filip Van Den Broeck, Sara Bargiacchi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 7, 2024
A cohort study of 19 patients with gyrate atrophy of the choroid and retina (GACR)Berith M Balfoort, Filip Van Den Broeck, Marion M Brands, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
Human Molecular Genetics|March 4, 2025
A novel recurrent ARL3 variant c.209G > A p.(Gly70Glu) causes variable non-syndromic dominant retinal dystrophy with defective lipidated protein transport in human retinal stem cell modelsJulio C Corral-Serrano, Veronika Vaclavik, Stijn Van de Sompele, et al.
Ophthalmology Science|March 21, 2025
Automated Cone Photoreceptor Detection in Adaptive Optics Flood Illumination OphthalmoscopySander Wooning, Pam A T Heutinck, Kubra Liman, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Stem Cell Research|November 6, 2025
Generation and characterization of three human induced pluripotent stem cell lines (UGENTi005, UGENTi006 and UGENTi007) from patients with autosomal dominant adult-onset maculopathy due to RPE65 variant c.1555G>A, p.(E519K)Eline Van Vooren, Filip Van den Broeck, Esperanza Daal, et al.
Investigative Ophthalmology & Visual Science|April 28, 2025
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt DiseaseJeroen A A H Pas, Catherina H Z Li, Filip Van den Broeck, et al.
Frontiers in Medicine|August 21, 2023
Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital ExperienceHwei Wuen Chan, Filip Van den Broeck, Axelle Cools, et al.
Surgical Innovation|January 23, 2019
Articulated Instruments and 3D Visualization: A Synergy? Evaluation of Execution Time, Errors, and Visual FatigueFrank Dewaele, Tim De Pauw, Nicolaas Lumen, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
Ophthalmic Genetics|December 5, 2022
Optic nerve involvement in <i>CACNA1F</i>-related disease: observations from a multicentric case seriesElisa Marziali, Filip Van Den Broeck, Sara Bargiacchi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 7, 2024
A cohort study of 19 patients with gyrate atrophy of the choroid and retina (GACR)Berith M Balfoort, Filip Van Den Broeck, Marion M Brands, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
Human Molecular Genetics|March 4, 2025
A novel recurrent ARL3 variant c.209G > A p.(Gly70Glu) causes variable non-syndromic dominant retinal dystrophy with defective lipidated protein transport in human retinal stem cell modelsJulio C Corral-Serrano, Veronika Vaclavik, Stijn Van de Sompele, et al.
Ophthalmology Science|March 21, 2025
Automated Cone Photoreceptor Detection in Adaptive Optics Flood Illumination OphthalmoscopySander Wooning, Pam A T Heutinck, Kubra Liman, et al.
Pageof 2