Results 31 to 40 of about 189,868 (219)

Retinal honeycomb appearance and its role in patients with X-linked retinoschisis. [PDF]

open access: yesBMC Ophthalmol, 2023
Background To investigate the clinical characteristics of retinal honeycomb appearance in a large cohort of patients with X-linked retinoschisis (XLRS) and to determine whether it is associated with complications like retinal detachment (RD) and vitreous
Ma J   +7 more
europepmc   +2 more sources

The dose-response relationship of subretinal gene therapy with rAAV2tYF-CB-h<i>RS1</i> in a mouse model of X-linked retinoschisis. [PDF]

open access: yesFront Med (Lausanne)
Purpose X-linked retinoschisis (XLRS), due to loss-of-function mutations in the retinoschisin (RS1) gene, is characterized by a modest to severe decrease in visual acuity.
Hassan S   +6 more
europepmc   +2 more sources

AAV2/4-RS1 gene therapy in the retinoschisin knockout mouse model of X-linked retinoschisis. [PDF]

open access: yesPLoS One, 2022
Objective To evaluate efficacy of a novel adeno-associated virus (AAV) vector, AAV2/4-RS1, for retinal rescue in the retinoschisin knockout (Rs1-KO) mouse model of X-linked retinoschisis (XLRS).
Scruggs BA   +8 more
europepmc   +2 more sources

Photoreceptor deficits appear at eye opening in Rs1 mutant mouse models of X-linked retinoschisis. [PDF]

open access: yesExp Eye Res
X-linked retinoschisis (XLRS) is an early onset degenerative retinal disease characterized by cystic lesions in the middle layers of the retina. These structural changes are accompanied by a loss of visual acuity and decreased contrast sensitivity.
Tarchick MJ   +4 more
europepmc   +2 more sources

Early recurrence of macular schisis in X-linked retinoschisis treated with vitrectomy for rhegmatogenous retinal detachment under silicone oil: case report and brief literature review. [PDF]

open access: yesTher Adv Ophthalmol
X-linked retinoschisis (XLRS) is an inherited retinal degeneration affecting males, characterized by splitting of the retinal layers. We herein present the outcomes of surgical treatment in a case of XLRS complicated by rhegmatogenous retinal detachment (
Stavrakas P   +7 more
europepmc   +2 more sources

Investigating the role of Caspase-1 in a mouse model of Juvenile X-linked Retinoschisis [PDF]

open access: yesFront Med (Lausanne)
Purpose Previous studies have reported Caspase-1 (Casp1) is upregulated in mouse models of Juvenile X-linked Retinoschisis (XLRS), however no functional role for Casp1 in disease progression has been identified.
Gehrke E   +6 more
europepmc   +2 more sources

Retinal Proteomic Alterations and Combined Transcriptomic-Proteomic Analysis in the Early Stages of Progression of a Mouse Model of X-Linked Retinoschisis [PDF]

open access: yesCells, 2022
X-linked retinoschisis (XLRS) is among the most commonly inherited degenerative retinopathies. XLRS is caused by functional impairment of RS1. However, the molecular mechanisms underlying RS1 malfunction remain largely uncharacterized. Here, we performed
Xiuxiu Jin   +10 more
doaj   +2 more sources

Retinal vasproliferative tumor in a case of X-linked retinoschisis detachment [PDF]

open access: yesAmerican Journal of Ophthalmology Case Reports, 2018
Purpose: To describe the first published case of X-linked retinoschisis (XLRS) detachment with retinal vasoproliferative tumor (RVPT) and provide a literature review of the subject.
Nimesh A. Patel   +5 more
doaj   +5 more sources

Dramatic response to topical dorzolamide in X-linked retinoschisis

open access: yesIndian Journal of Ophthalmology, 2020
Macular involvement is commonly seen in cases with X-linked retinoschisis (XLRS) which includes foveal schisis and cystic maculopathy. Although no definitive treatment has been described, the use of topical 2% dorzolamide hydrochloride in such cases has ...
Rajeswari Thangavel   +3 more
doaj   +2 more sources

Exudative maculopathy in presumed X-linked retinoschisis with review of literature [PDF]

open access: yesIndian Journal of Ophthalmology, 2022
Srishti Ramamurthy   +3 more
doaj   +2 more sources

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