Biedru informācija
Pr Camiel BOON
Nīderlande
Komanda
Dr Axel PETZOLD
Nīderlande
HCP centrs
kontakts
Amsterdam University Medical Center / Leiden University Medical Center
Klīniskie izmēģinājumi
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
Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene
Phase 3 Follow-up Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR Gene
Half-dose photodynamic therapy versus eplerenone treatment in chronic centralserous chorioretinopathy.
Natural history of the progression of X-linked retinitis pigmentosa.
A multi-national, multi-centre, double-masked, placebo-controlled proof of concept trial to evaluate the safety and efficacy of oral soraprazan in Stargardt disease
Prospective Clinical Trial to Evaluate the Efficacy of Acetazolamide for the Treatment of Cystoid Fluid Collections in Retinoschisis: The AXIS Trial
A Two-Year Double-masked, Randomized, Sham-Controlled 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
Zinātniskās publikācijas
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
Van de Sompele et al. izmantoja multiomikas profilēšanu un in vitro un in vivo pastiprinātāju testus, lai izdalītu regulējošos mehānismus, kas ir pamatā Ziemeļu ...
Novel Clinical Observations and Genetic Spectrum in 340 Patients
Lielākajai daļai pacientu XLRS uzrādīja lēnu pasliktināšanos, sākot ar otro dzīves desmitgadi, kas liecina par optimālu iespēju...
Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa
Novērtēt kataraktas operācijas vizuālo iznākumu pacientiem ar pigmentozo retinītu...
The Natural History of Leber Congenital Amaurosis and ConeeRod Dystrophy Associated with Variants in the GUCY2D Gene
Lēbera iedzimtā amauroze, kas saistīta ar GUCY2D, funduskopijā izraisīja smagus iedzimtus redzes traucējumus ar salīdzinoši neskartu makulas anatomiju...
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
Pacientiem ar nepareizām izmaiņām bija labāka BCVA un lielāka strukturālā integritāte. Tas ir svarīgi pacientu prognozēšanai un...
Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 Mutations
Izpētīt dabisko vēsturi pacientiem ar LRAT- saistītās tīklenes deģenerācijas (RD) klīnisko izmēģinājumu testēšanas laikā...
Central serous chorioretinopathy: Towards an evidence-based treatment guideline
Līdz šim nav panākta vienprātība par CSC klasifikāciju, un ir ierosināti dažādi iejaukšanās pasākumi, kas atspoguļo...
Syndromic Retinitis Pigmentosa
Clinical, Genetic, and Histopathological Characteristics of CRX-associated Retinal Dystrophies
Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries: An International Survey by the European Vision Institute
Efficacy of Carbonic Anhydrase Inhibitors on Cystoid Fluid Collections and Visual Acuity in Patients with X-Linked Retinoschisis
Mūsu dati liecina, ka ārstēšana ar (orālo) CAI var būt noderīga īslaicīgai CFC ārstēšanai pacientiem ar...