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Retinitis pigmentosa is a common hereditary retinaldisease that leads to blindness.
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Lund said the same could be done in people with retinaldisease.
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However, few nonhuman primate models of genetic retinaldisease are known.
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Ultimately these tools should be useful in predicting retinaldisease progression.
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These successes notwithstanding, most other genetic retinaldisease will be refractory to supplementation.
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Congenital stationary night blindness (CSNB) is a nonprogressive retinaldisorder that can be associated with impaired night vision.
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Achromatopsia is an inherited retinaldisorder of cone photoreceptors characterized by markedly reduced visual acuity, extreme light sensitivity, and absence of color discrimination.
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Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous group of non-progressive retinaldisorder with largely normal fundus appearance.
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Degeneration of RPE cells results in retinaldisorders such as age-related macular degeneration.
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Mutations in ABCA4 cause Stargardt disease and other blinding autosomal recessive retinaldisorders.
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The impairment is not due to developmental retinaldefect.
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Methods: This prospective cross-sectional study included 24 children previously treated with VGB and monitored in early childhood by electroretinogram for VGB-attributed retinaldefects.
Usage of retinal diseases in English
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Background: Many retinaldiseases are associated with vascular dysfunction accompanied by neuroinflammation.
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These results may help as we begin to understand certain age-related retinaldiseases.
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Furthermore, implications drawn from these models for gene therapy in retinaldiseases are discussed.
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Specific cone-directed therapy is of high priority in the treatment of human hereditary retinaldiseases.
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The findings also suggest that the therapeutical possibilities of PARP inhibition should include retinaldiseases like RP.
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Purpose: Inflammation associated with blood- retinal barrier (BRB) breakdown is a common feature of several retinaldiseases.
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Despite the rare occurrence of PEHCR, it must be included in the differential diagnosis for peripheral retinaldiseases.
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In retinaldiseases, there can be invasion by Iba1-positive cells, which can be detected by noninvasive imaging techniques.
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Alterations of retinoid cycle genes are known to cause retinaldiseases characterized by focal white dot fundus lesions.
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However, these data demonstrated that they present different expression profiles in the tissues, in retinal development, and in retinaldiseases.
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The new instrument is controlled by a personal computer and can be used in the investigation of several retinaldiseases.
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To date over 60 different mutations have been reported in human retinaldiseases, with most being restricted to single families.
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A broad spectrum of retinaldiseases affects both the retinal vasculature and the neural retina, including photoreceptor and postreceptor layers.
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It is focused on three areas of unmet medical needs, including inherited retinaldiseases, severe forms of xerostomia and neurodegenerative diseases.
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Breakdown of the blood- retinal barrier (BRB) occurs in several retinaldiseases and is a major cause of visual loss.
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Retinitis pigmentosa (RP) is a group of genetically and clinically heterogeneous retinaldiseases and a common cause of blindness.