Informações do membro
Dr Ingeborgh VAN DEN BORN
Netherlands
Centro de saúde
Contacto
The Rotterdam Eye Hospital, Rotterdam, Netherlands
Ensaios clínicos
A Double-Masked, Randomized, Controlled, Multiple-Dose Study to Evaluate the Efficacy, Safety and Tolerability of Ultevursen in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene (Sirius)
Steroid Eye Drops Versus Placebo Eye Drops in Chronic Central Serous Chorioretinopathy Trial (PICS Trial)
Natural History Study in Subjects With Usher Syndrome.
Historical Case Record Survey of Visual Acuity Data From Patients With Leber’s Hereditary Optic Neuropathy (LHON).
Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT.
A Phase III, Multicenter, Randomized, Double-Masked, Sham-Controlled Study to Investigate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Vamikibart Administered Intravitreally in Patients With Uveitic Macular Edema
A Multicenter, Prospective, Longitudinal, Observational Study in Children and Adults With Stargardt Disease Related Atrophy Secondary to Biallelic Mutations in the ABCA4 Gene
Publicações científicas
Novel Clinical Observations and Genetic Spectrum in 340 Patients
Na maioria dos pacientes, a XLRS mostrou uma deterioração lenta a partir da segunda década de vida, sugerindo uma janela de oportunidade ideal para...
The Natural History of Leber Congenital Amaurosis and ConeeRod Dystrophy Associated with Variants in the GUCY2D Gene
A amaurose congênita de Leber associada ao GUCY2D causou grave deficiência visual congênita com anatomia macular relativamente intacta na fundoscopia...
Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network – EVICR.net
Este segundo inquérito multinacional sobre a gestão de IRD na Europa destaca diferenças importantes e persistentes no número de pacientes com IRD tratados...
Current Management of Patients with RPE65 Mutation Associated Inherited Retinal Degenerations in Europe: Results of a 2-Year Follow-Up Multinational Survey
Um questionário eletrônico de pesquisa com 48 perguntas abordando especificamente o RPE65-IRD (pesquisa 2019 de 35) foi desenvolvido e enviado até junho de 2021 para 95...
Efficacy of Carbonic Anhydrase Inhibitors on Cystoid Fluid Collections and Visual Acuity in Patients with X-Linked Retinoschisis
Nossos dados indicam que o tratamento com CAI (oral) pode ser benéfico para o manejo de curto prazo do CFC em pacientes com...