Meanings of retinal diseases in English

Background: Many retinal diseases are associated with vascular dysfunction accompanied by neuroinflammation.

These results may help as we begin to understand certain age-related retinal diseases.

Furthermore, implications drawn from these models for gene therapy in retinal diseases are discussed.

Specific cone-directed therapy is of high priority in the treatment of human hereditary retinal diseases.

The findings also suggest that the therapeutical possibilities of PARP inhibition should include retinal diseases like RP.

Purpose: Inflammation associated with blood- retinal barrier (BRB) breakdown is a common feature of several retinal diseases.

Despite the rare occurrence of PEHCR, it must be included in the differential diagnosis for peripheral retinal diseases.

In retinal diseases, there can be invasion by Iba1-positive cells, which can be detected by noninvasive imaging techniques.

Alterations of retinoid cycle genes are known to cause retinal diseases characterized by focal white dot fundus lesions.

However, these data demonstrated that they present different expression profiles in the tissues, in retinal development, and in retinal diseases.

The new instrument is controlled by a personal computer and can be used in the investigation of several retinal diseases.

To date over 60 different mutations have been reported in human retinal diseases, with most being restricted to single families.

A broad spectrum of retinal diseases affects both the retinal vasculature and the neural retina, including photoreceptor and postreceptor layers.

It is focused on three areas of unmet medical needs, including inherited retinal diseases, severe forms of xerostomia and neurodegenerative diseases.

Breakdown of the blood- retinal barrier (BRB) occurs in several retinal diseases and is a major cause of visual loss.

Retinitis pigmentosa (RP) is a group of genetically and clinically heterogeneous retinal diseases and a common cause of blindness.