Liikmete teave
Pr Camiel BOON
Holland
meeskond
Dr Axel PETZOLD
Holland
HCP keskus
kontakt
Amsterdam University Medical Center / Leiden University Medical Center
Kliinilised uuringud
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
Teaduslikud väljaanded
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
Van de Sompele jt. kasutas multiomika profiilide koostamist ning in vitro ja in vivo võimendajateste, et lahkada Põhja-Ameerika aluseks olevaid regulatiivseid mehhanisme.
Novel Clinical Observations and Genetic Spectrum in 340 Patients
Enamikul patsientidel näitas XLRS aeglast halvenemist alates teisest elukümnendist, mis viitab optimaalsele võimalusele...
Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa
Et hinnata katarakti operatsiooni visuaalset tulemust pigmentosa retiniidiga patsientidel...
The Natural History of Leber Congenital Amaurosis and ConeeRod Dystrophy Associated with Variants in the GUCY2D Gene
GUCY2D-ga seotud Leberi kaasasündinud amauroos põhjustas funduskoopial raske kaasasündinud nägemiskahjustuse suhteliselt puutumata makulaarse anatoomiaga ...
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
Missense muutustega patsientidel oli parem BCVA ja suurem struktuurne terviklikkus. See on oluline patsiendi prognoosimiseks ja...
Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 Mutations
Loodusliku ajaloo uurimiseks patsientidel, kellel on LRAT-seotud võrkkesta degeneratsioonid (RD-d) kliiniliste uuringute tulekul...
Central serous chorioretinopathy: Towards an evidence-based treatment guideline
Siiani ei ole CSC klassifikatsiooni osas üksmeelele jõutud ja pakutud on mitmesuguseid sekkumisi, mis peegeldavad ...
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
Meie andmed näitavad, et ravi (suukaudse) CAI-ga võib olla kasulik CFC lühiajaliseks raviks patsientidel, kellel on...