Применение закона Вебера-Фехнера в квантовой электроретинографии [PDF]
, 2015 Адаптовано метод електроретинографії до задачі виявлення ризиків нейротоксикації, шляхом підвищення чутливості методу при зниженні енергії світлового подразнення, і переходу до квантової електроретинографії, що дало можливість проводити ідентифікацію ...
Демчук, Любомир Богданович +3 more
core
Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy. [PDF]
, 2015 Inherited retinal dystrophies present extensive phenotypic and genetic heterogeneity, posing a challenge for patients' molecular and clinical diagnoses.
Avila-Fernandez, A. +10 more
core +2 more sources
Visual acuity and rod function in patients with retinitis pigmentosa [PDF]
, 2004 PURPOSE: To investigate visual acuity and rod function, and correlate them to different clinical parameters in patients with retinitis pigmentosa (RP).
Berezovsky, Adriana +4 more
core +4 more sources
Loss of synchronized retinal phagocytosis and age-related blindness in mice lacking alphavbeta5 integrin. [PDF]
, 2004 Daily phagocytosis by the retinal pigment epithelium (RPE) of spent photoreceptor outer segment fragments is critical for vision. In the retina, early morning circadian photoreceptor rod shedding precedes synchronized uptake of shed photoreceptor ...
Brodie, Scott E +5 more
core +1 more source
PACAP application improves functional outcome of chronic retinal ischemic injury in rats – evidence from electroretinographic measurements [PDF]
, 2014 Retinoprotective effects of pituitary adenylate cyclase activating polypeptide (PACAP) are well-known and have been demonstrated in various pathological conditions, such as diabetic retinopathy, excitotoxic retinal injury, UV light-induced degeneration ...
Batai, István +10 more
core +1 more source
Familial cases of a submicroscopic Xp22.2 deletion : genotype-phenotype correlation in microphthalmia with linear skin defects syndrome [PDF]
, 2013 Purpose: Microphthalmia with linear skin defects syndrome (MLS or MIDAS, OMIM #309801) is a rare X-linked male-lethal disorder characterized by microphthalmia or other ocular anomalies and skin lesions limited to the face and neck.
Claerhout, Ilse +3 more
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Galician Medical Journal, 2016 Primary glaucoma is a disease causing the greatest number of vision-related problems. Accelerated death of retinal ganglion cells and their axons which comprise the optic nerve as well as their involvement in the pathological process of neuroglia which ...
L. M. Stotska
doaj
Correction of retinal ischemia/reperfusion by 3-(1H-benzimidazol-2-il)-1,2,2-trimethyl cyclopentancarbonic acid in experiment [PDF]
, 2018 Results of ocular fundus studies revealed the most pronounced protective effects of 3-(1Hbenzimidazol-2-il)-1,2,2-trimethyl cyclopentancarbonic acid in a dose 50 mg/kg on the model of retinal ischemiareperfusion in Wistar rats, which is reflected in the ...
Bunyatyan, N. D. +4 more
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Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiency [PDF]
, 2009 In mammals, increased GABA in the central nervous system has been associated with abnormalities of visual evoked potentials (VEPs), predominantly manifested as increased latency of the major positive component P100.
Blasi, P +7 more
core +1 more source
Journal of Ophthalmology, 2018 Background: Rhegmatogenous retinal detachment (RRD) is a serious incapacitating disease requiring surgical treatment. Trophic disturbances in the central and peripheral retina are characteristic for myopia, which is known to be a major risk factor for ...
Alibet Yassine +3 more
doaj +1 more source