Lessons Learned: Quality Analysis of Optical Coherence Tomography in Neuromyelitis Optica
ABSTRACT Introduction Optical coherence tomography (OCT)‐derived retina measurements are markers for neuroaxonal visual pathway status. High‐quality OCT scans are essential for reliable measurements, but their acquisition is particularly challenging in eyes with severe visual impairment, as often observed in neuromyelitis optica spectrum disorders ...
Hadi Salih +40 more
wiley +1 more source
Role of fundus autofluorescence imaging in the management of submacular hemorrhage
Purpose To evaluate the baseline characteristics of fundus autofluorescence (FAF) in patients with submacular hemorrhage (SMH). Methods This retrospective study included patients diagnosed with treatment-naive, foveal-involving subretinal hemorrhage ...
Ramesh Venkatesh +10 more
doaj +1 more source
Human visual response to nuclear particle exposures [PDF]
Experiments with accelerated helium ions were performed in an effort to localize the site of initial radiation interactions in the eye that lead to light flash observations by astronauts during spaceflight.
Budinger, T. F. +2 more
core +1 more source
Retina as a potential biomarker in schizophrenia spectrum disorders: a systematic review and meta-analysis of optical coherence tomography and electroretinography [PDF]
Hiroshi Komatsu +10 more
openalex +1 more source
The expression of serotonin (5-HT) in the retina was first reported in the sixties. The detection of vesicular monoamine transporter and serotonin receptors in several retinal cells confirm that 5-HT is playing a neuromodulatory role in this structure.
openaire +4 more sources
High-resolution analysis of the human retina miRNome reveals isomiR variations and novel microRNAs
MicroRNAs play a fundamental role in retinal development and function. To characterise the miRNome of the human retina, we carried out deep sequencing analysis on sixteen individuals.
M. Karali +13 more
semanticscholar +1 more source
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
A 50-year-old male patient with sudden visual acuity loss in his right eye came to our clinic. Visual acuity at presentation was 1/10 in right eye and 10/10 in left. The patient was otherwise healthy Caucasian man without any history of previous systemic
Narges Hassanpoor +2 more
doaj +1 more source
Retinal adaptation of Japanese common squid (Todarodes pacificus Steenstrup) to light changes [PDF]
The response of retinae of the Japanese common squid (Todarodes pacificus Steenstrup) was recorded in relation to various light intensities. In the light-adapted eye of common squid, the black pigment ascends to the external limiting membrance of the ...
Hiroshi, Inada +2 more
core
Large-scale multielectrode recording and stimulation of neural activity [PDF]
Large circuits of neurons are employed by the brain to encode and process information. How this encoding and processing is carried out is one of the central questions in neuroscience.
Chichilnisky, E. J. +10 more
core +1 more source

