Joseph Van Aerschot
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 8 publications
Isolated ocular relapse in pediatric acute lymphoblastic leukemia: a case report.
Journal: Digital journal of ophthalmology : DJO
Published: August 11, 2026
Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa.
Journal: Molecular medicine (Cambridge, Mass.)
Published: February 03, 2026
Late diagnosis of Heimler syndrome and review of the genetic and phenotypic spectrum.
Journal: Ophthalmic genetics
Published: October 23, 2025
A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry.
Journal: Investigative ophthalmology & visual science
Published: July 01, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.
Journal: medRxiv : the preprint server for health sciences
Published: January 20, 2025
Showing 1-8 of 8
Last Updated: 09/26/2026