Julie Jacob
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
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Found 31 publications
Late diagnosis of Heimler syndrome and review of the genetic and phenotypic spectrum.
Journal: Ophthalmic genetics
Published: October 23, 2025
RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected Individuals.
Journal: Investigative ophthalmology & visual science
Published: September 23, 2025
RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals.
Journal: Research square
Published: May 19, 2025
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy.
Journal: American journal of human genetics
Published: September 12, 2024
Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants.
Journal: Clinical genetics
Published: May 13, 2024
A rare presentation of a common carotid artery occlusion.
Journal: GMS ophthalmology cases
Published: December 19, 2023
RESOLUTION OF CHOROIDAL METASTASIS AND ASSOCIATED SUBRETINAL EXUDATION OF METASTATIC CUTANEOUS MELANOMA 15 DAYS AFTER TREATMENT WITH COMBINED TARGETED THERAPY.
Journal: Retinal cases & brief reports
Published: September 27, 2023
VOGT-KOYANAGI-HARADA DISEASE-LIKE UVEITIS IN A PATIENT WITH ADVANCED MELANOMA TREATED BY SEQUENTIAL ADMINISTRATION OF NIVOLUMAB AND DABRAFENIB/TRAMETINIB THERAPY.
Journal: Retinal cases & brief reports
Published: August 29, 2023
Unilateral Melanoma-Associated Retinopathy Case Report.
Journal: Case reports in ophthalmology
Published: May 22, 2023
Brolucizumab for Neovascular Age-Related Macular Degeneration (BEL Study).
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: January 24, 2023
Artificial Intelligence Software for Diabetic Eye Screening: Diagnostic Performance and Impact of Stratification.
Journal: Journal of clinical medicine
Published: January 03, 2023
Last Updated: 09/26/2026