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Dr Camiel BOON

In this page

Member info

Dr Camiel BOON

Representative

Netherlands

Working Group Leader: Research (TWG8)
Other Working Group(s): Retinal Rare Eye Diseases (WG1), Pediatric Ophthalmology Rare Diseases (WG3), Anterior Segment Rare Eye Diseases (WG4), Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7), Research (TWG8), National Integration (TWG9)

Team

Dr Axel PETZOLD

Netherlands

Neuro-Ophthalmology Rare Diseases (WG2), Research (TWG8)
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Dr Lucas Wenninger

Netherlands

Neuro-Ophthalmology Rare Diseases (WG2)
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HCP Center

LUMC / AMC are modern university medical centers for research, education and patient care with a high quality profile and a strong scientific...

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Leiden University Medical Center/Academic Medical Center Amsterdam, Netherlands

Albinusdreef 2
2333 ZA Leiden
Netherlands

Clinical trials

NCT05537220 Active, Not recruiting

NAC Attack, A Phase III, Multicenter, Randomized, Parallel, Double Masked, Placebo-Controlled Study Evaluating the Efficacy and Safety of Oral N-Acetylcysteine in Patients With Retinitis Pigmentosa

Interventional
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NCT04671433 Active, Not recruiting

Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene

Interventional
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NCT04794101 Active, Not recruiting

Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene

Interventional
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NCT03079141 Unknown

Half-dose photodynamic therapy versus eplerenone treatment in chronic centralserous chorioretinopathy.

Interventional
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Scientific publications

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

Van de Sompele et al. used multiomics profiling and in vitro and in vivo enhancer assays to dissect the regulatory mechanisms underlying North...

Novel Clinical Observations and Genetic Spectrum in 340 Patients

In most patients, XLRS showed a slow deterioration starting in the second decade of life, suggesting an optimal window of opportunity for...

Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa

To assess the visual outcome of cataract surgery in patients with retinitis pigmentosa...

The Natural History of Leber Congenital Amaurosis and ConeeRod Dystrophy Associated with Variants in the GUCY2D Gene

Leber congenital amaurosis associated with GUCY2D caused severe congenital visual impairment with relatively intact macular anatomy on funduscopy...

Repeatability of Quantitative Autofluorescence Imaging in a Multicenter Study Involving Patients With Recessive Stargardt Disease 1

KCNV2-associated retinopathy: genotype-phenotype correlations – KCNV2 study group report 3

Patients with missense alterations had better BCVA and greater structural integrity. This is important for patient prognostication and...

Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 Mutations

To investigate the natural history in patients with LRAT-associated retinal degenerations (RDs), in the advent of clinical trials testing...

Central serous chorioretinopathy: Towards an evidence-based treatment guideline

To date, no consensus has been reached regarding the classification of CSC, and a wide variety of interventions have been proposed, reflecting the...