Documenta Ophthalmologica

Papers
(The TQCC of Documenta Ophthalmologica is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
ISCEV Standard for full-field clinical electroretinography (2022 update)245
ISCEV standard for clinical multifocal electroretinography (mfERG) (2021 update)99
Retinal function after intravitreal injection of autologous bone marrow-derived mesenchymal stromal cells in advanced glaucoma21
Electroretinogram responses in myopia: a review18
Unilateral optic neuritis after vaccination against the coronavirus disease: two case reports17
Case with metastatic cutaneous malignant melanoma that developed Vogt–Koyanagi–Harada-like uveitis following pembrolizumab treatment14
Reference ranges for clinical electrophysiology of vision12
Continuous wavelet transform analysis of ERG in patients with diabetic retinopathy11
ISCEV guidelines for calibration and verification of stimuli and recording instruments (2023 update)10
ISCEV standard for clinical pattern electroretinography (2024 update)10
Associations between steady-state pattern electroretinography and estimated retinal ganglion cell count in glaucoma suspects8
The contribution of multifocal visual evoked potentials in patients with optic neuritis and multiple sclerosis: a review8
A new PDE6A missense variant p.Arg544Gln in rod–cone dystrophy7
The acute effect of atropine eye drops on the human full-field electroretinogram7
Electronegative ERG or pseudo-negative ERG?6
Pediatric abusive head trauma: visual outcomes, evoked potentials, diffusion tensor imaging, and relationships to retinal hemorrhages6
Monitoring for glaucoma progression with SAP, electroretinography (PERG and PhNR) and OCT6
Structure–function models for estimating retinal ganglion cell count using steady-state pattern electroretinography and optical coherence tomography in glaucoma suspects and preperimetric glaucoma: an5
Vogt-Koyanagi-Harada syndrome-like uveitis after nivolumab administration as a treatment for ovarian cancer5
Correlation between electroretinography, foveal anatomy and visual acuity in aniridia due to PAX6 mutations5
Comparing the RETeval® portable ERG device with more traditional tabletop ERG systems in normal subjects and selected retinopathies5
Pattern ERGs suggest a possible retinal contribution to the visual acuity loss in acute optic neuritis5
60th Annual Symposium of the International Society for Clinical Electrophysiology of Vision (ISCEV 2023 Kyoto)5
Proliferative diabetic retinopathy treated with intravitreal ranibizumab and photocoagulation directed at ischemic retinal areas—A randomized study5
Short-term delay in neural response with multifocal contact lens might start at the retinal level5
Long-term follow-up of a patient with JAG1-associated retinopathy5
Bilateral compressive optic neuropathy and outer retinopathy due to optic canal hyperostosis in a child with isolated vitamin a deficiency5
Evaluation of the neuronal and microvascular components of the macula in patients with diabetic retinopathy5
Correlations among metamorphopsia test scores, optical coherence tomography findings and multifocal electroretinogram responses in epiretinal membrane patients5
Flicker electroretinogram in newborn infants4
A patient diagnosed with Galloway–Mowat syndrome presenting with a rod-cone functional anomaly with electronegative dark-adapted ERGs4
Use of an alternating current amplifier when recording the ERG c-wave to evaluate the function of retinal pigment epithelial cells in rats4
Documentation of recovery from vitamin A deficiency-related retinopathy via multimodal imaging and electroretinogram testing4
Anti-angiogenic activity and safety of intraocular application of triterpenes4
Assessment of digital light processing (DLP) projector stimulators for visual electrophysiology4
Age-associated changes in electroretinography measures in companion dogs4
Electrophysiological assessment of nutritional optic neuropathy: a case report4
Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese family4
Foveal avascular zone size and mfERG metrics in diabetes and prediabetes: a pilot study of the relationship between structure and function4
MERCI: a machine learning approach to identifying hydroxychloroquine retinopathy using mfERG4
VEP examination with new portable device4
Intravitreal acetazolamide implant for pseudophakic cystoid macular edema4
Compound Heterozygous Mutations in ZNF408 in a Patient with a Late Onset Pigmentary Retinopathy and Relatively Preserved Central Retina3
Accelerated hydroxychloroquine toxic retinopathy3
Fundus autofluorescence, optical coherence tomography and electroretinography abnormalities in a patient with digoxin retinopathy that resemble those in KCNV2-associated retinopathy3
Use of extended protocols with nonstandard stimuli to characterize rod and cone contributions to the canine electroretinogram3
A novel system for measuring visual potentials evoked by passive head-mounted display stimulators3
New criteria for evaluation of electroretinogram in patients with retinitis pigmentosa3
The influence of temporal frequency and stimulus size on the relative contribution of luminance and L-/M-cone opponent mechanisms in heterochromatic flicker ERGs3
Residual rod function in CNGB1 mutant dogs3
Melanoma-associated retinopathy with anti-TRPM1 autoantibodies showing concomitant Off-bipolar cell dysfunction3
Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy3
Rod photoreceptor activation and deactivation in early-stage diabetic eye disease3
The second Japanese family with Malattia Leventinese/Doyne honeycomb retinal dystrophy3
Qualitative and quantitative comparison of ERGs with contact lens and adhesive skin electrodes3
Visual function during and after an acute central serous chorioretinopathy episode3
Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report3
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