[HTML][HTML] Non-syndromic retinitis pigmentosa
SK Verbakel, RAC van Huet, CJF Boon… - Progress in retinal and …, 2018 - Elsevier
Retinitis pigmentosa (RP) encompasses a group of inherited retinal dystrophies
characterized by the primary degeneration of rod and cone photoreceptors. RP is a leading …
characterized by the primary degeneration of rod and cone photoreceptors. RP is a leading …
[HTML][HTML] Venous overload choroidopathy: A hypothetical framework for central serous chorioretinopathy and allied disorders
RF Spaide, CMG Cheung, H Matsumoto, S Kishi… - Progress in retinal and …, 2022 - Elsevier
In central serous chorioretinopathy (CSC), the macula is detached because of fluid leakage
at the level of the retinal pigment epithelium. The fluid appears to originate from choroidal …
at the level of the retinal pigment epithelium. The fluid appears to originate from choroidal …
The spectrum of ocular phenotypes caused by mutations in the BEST1 gene
CJF Boon, BJ Klevering, BP Leroy, CB Hoyng… - Progress in retinal and …, 2009 - Elsevier
Bestrophin-1 is an integral membrane protein, encoded by the BEST1 gene, which is
located in the basolateral membrane of the retinal pigment epithelium. The bestrophin-1 …
located in the basolateral membrane of the retinal pigment epithelium. The bestrophin-1 …
[HTML][HTML] Central serous chorioretinopathy: towards an evidence-based treatment guideline
TJ Van Rijssen, EH Van Dijk, S Yzer… - Progress in retinal and …, 2019 - Elsevier
Central serous chorioretinopathy (CSC) is a common cause of central vision loss, primarily
affecting men 20–60 years of age. To date, no consensus has been reached regarding the …
affecting men 20–60 years of age. To date, no consensus has been reached regarding the …
Association of axial length with risk of uncorrectable visual impairment for Europeans with myopia
JWL Tideman, MCC Snabel, MS Tedja… - JAMA …, 2016 - jamanetwork.com
Importance Myopia (ie, nearsightedness) is becoming the most common eye disorder to
cause blindness in younger persons in many parts of the world. Visual impairment due to …
cause blindness in younger persons in many parts of the world. Visual impairment due to …
[HTML][HTML] Half-dose photodynamic therapy versus high-density subthreshold micropulse laser treatment in patients with chronic central serous chorioretinopathy: the …
EHC van Dijk, S Fauser, MB Breukink… - Ophthalmology, 2018 - Elsevier
Purpose To compare the anatomic and functional efficacy and safety of half-dose
photodynamic therapy (PDT) versus high-density subthreshold micropulse laser (HSML) …
photodynamic therapy (PDT) versus high-density subthreshold micropulse laser (HSML) …
Central serous chorioretinopathy: an update on risk factors, pathophysiology and imaging modalities
Central serous chorioretinopathy (CSC) is a common form of vision loss, typically seen in
working-age men. The pathophysiology behind CSC still eludes us, however significant …
working-age men. The pathophysiology behind CSC still eludes us, however significant …
The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene
CJF Boon, AI den Hollander, CB Hoyng… - Progress in retinal and …, 2008 - Elsevier
Peripherin/rds is an integral membrane glycoprotein, mainly located in the rod and cone
outer segments. The relevance of this protein to photoreceptor outer segment morphology …
outer segments. The relevance of this protein to photoreceptor outer segment morphology …
Risk alleles in CFH and ARMS2 are independently associated with systemic complement activation in age-related macular degeneration
D Smailhodzic, CCW Klaver, BJ Klevering, CJF Boon… - Ophthalmology, 2012 - Elsevier
PURPOSE: Systemic complement activation is associated with age-related macular
degeneration (AMD) and has mainly been attributed to a risk allele in the complement factor …
degeneration (AMD) and has mainly been attributed to a risk allele in the complement factor …
Clinical and genetic characteristics of late-onset Stargardt's disease
SC Westeneng-van Haaften, CJF Boon, FPM Cremers… - Ophthalmology, 2012 - Elsevier
OBJECTIVE: To describe the genotype and phenotype of patients with a late-onset
Stargardt's disease (STGD1). DESIGN: Retrospective case series. PARTICIPANTS: Twenty …
Stargardt's disease (STGD1). DESIGN: Retrospective case series. PARTICIPANTS: Twenty …