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Quoted phrase not found in phrase index: "Retinitis pigmentosa 70"
Page 1
Approach to inherited retinal diseases.
Ratra D, Ozdek S, Raviselvan M, Elchuri S, Sharma T. Ratra D, et al. Indian J Ophthalmol. 2022 Jul;70(7):2305-2315. doi: 10.4103/ijo.IJO_314_22. Indian J Ophthalmol. 2022. PMID: 35791111 Free PMC article. Review.
It would help to familiarize oneself about how to approach a patient with an IRD. An early and accurate diagnosis can help predict the vision loss and also help the patient plan his/her education and choose appropriate career choices. ...
It would help to familiarize oneself about how to approach a patient with an IRD. An early and accurate diagnosis can help predict th …
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History.
Georgiou M, Robson AG, Jovanovic K, Guimarães TAC, Ali N, Pontikos N, Uwaydat SH, Mahroo OA, Cheetham ME, Webster AR, Hardcastle AJ, Michaelides M. Georgiou M, et al. Ophthalmology. 2023 Apr;130(4):413-422. doi: 10.1016/j.ophtha.2022.11.015. Epub 2022 Nov 22. Ophthalmology. 2023. PMID: 36423731 Free PMC article.
Twenty-eight disease-causing variants were identified, with 20 not previously clinically characterized. Fifty-three patients (98.1%) presented with retinitis pigmentosa. The mean age of onset (range standard deviation [SD]) was 9.6 years (1-57 9.2 years). ...Pattern …
Twenty-eight disease-causing variants were identified, with 20 not previously clinically characterized. Fifty-three patients (98.1%) present …
Association of Circulating Antiretinal Antibodies With Clinical Outcomes in Retinitis Pigmentosa.
Bianco L, Arrigo A, Antropoli A, Del Fabbro S, Panina-Bordignon P, Peri C, Brambilla E, Pina A, Basile G, Hassan Farah R, Saladino A, Aragona E, Cascavilla ML, Bandello F, Battaglia Parodi M, Pulido JS. Bianco L, et al. Invest Ophthalmol Vis Sci. 2023 Dec 1;64(15):13. doi: 10.1167/iovs.64.15.13. Invest Ophthalmol Vis Sci. 2023. PMID: 38088826 Free PMC article.
PURPOSE: To determine if circulating antiretinal antibodies (ARAs) differ between patients affected by retinitis pigmentosa (RP) and control participants and to assess whether ARAs are associated with clinical outcomes in patients with RP. ...Overall, at least one A …
PURPOSE: To determine if circulating antiretinal antibodies (ARAs) differ between patients affected by retinitis pigmentosa (R …
Retinal oximetry: Metabolic imaging for diseases of the retina and brain.
Stefánsson E, Olafsdottir OB, Eliasdottir TS, Vehmeijer W, Einarsdottir AB, Bek T, Torp TL, Grauslund J, Eysteinsson T, Karlsson RA, Van Keer K, Stalmans I, Vandewalle E, Todorova MG, Hammer M, Garhöfer G, Schmetterer L, Šín M, Hardarson SH. Stefánsson E, et al. Prog Retin Eye Res. 2019 May;70:1-22. doi: 10.1016/j.preteyeres.2019.04.001. Epub 2019 Apr 15. Prog Retin Eye Res. 2019. PMID: 30999027 Review.
This provides an objective biomarker for glaucomatous damage. In retinitis pigmentosa, an association exists between advanced atrophy, worse visual field and higher retinal venous oxygen saturation, lower arteriovenous difference. This biomarker may allow measuremen …
This provides an objective biomarker for glaucomatous damage. In retinitis pigmentosa, an association exists between advanced …
Disease asymmetry and hyperautofluorescent ring shape in retinitis pigmentosa patients.
Jauregui R, Chan L, Oh JK, Cho A, Sparrow JR, Tsang SH. Jauregui R, et al. Sci Rep. 2020 Feb 25;10(1):3364. doi: 10.1038/s41598-020-60137-9. Sci Rep. 2020. PMID: 32098976 Free PMC article.
Retinitis pigmentosa (RP) is described as a bilateral disease with inter-eye symmetry that presents on short-wavelength fundus autofluorescence (SW-AF) imaging with hyperautofluorescent (hyperAF) rings with an ellipsoid shape and regular borders. ...We observed …
Retinitis pigmentosa (RP) is described as a bilateral disease with inter-eye symmetry that presents on short-wavelength fundus …
Management of retinitis pigmentosa by Wharton's jelly derived mesenchymal stem cells: preliminary clinical results.
Özmert E, Arslan U. Özmert E, et al. Stem Cell Res Ther. 2020 Jan 13;11(1):25. doi: 10.1186/s13287-020-1549-6. Stem Cell Res Ther. 2020. PMID: 31931872 Free PMC article.
PURPOSE: The aim of this study is to determine if umbilical cord Wharton's jelly derived mesenchymal stem cells implanted in sub-tenon space have beneficial effects on visual functions in retinitis pigmentosa patients by reactivating the degenerated photoreceptors i …
PURPOSE: The aim of this study is to determine if umbilical cord Wharton's jelly derived mesenchymal stem cells implanted in sub-tenon space …
Classification of disease severity in retinitis pigmentosa.
Iftikhar M, Lemus M, Usmani B, Campochiaro PA, Sahel JA, Scholl HPN, Shah SMA. Iftikhar M, et al. Br J Ophthalmol. 2019 Nov;103(11):1595-1599. doi: 10.1136/bjophthalmol-2018-313669. Epub 2019 Jan 31. Br J Ophthalmol. 2019. PMID: 30705041
AIM: To develop a simple and easily applicable classification of disease severity in retinitis pigmentosa (RP). METHODS: This is a retrospective cross-sectional study. ...A scoring criterion was developed wherein each variable was assigned a score from 0 to 5 …
AIM: To develop a simple and easily applicable classification of disease severity in retinitis pigmentosa (RP). METHODS: This …
Next-generation sequencing--based genetic testing and phenotype correlation in retinitis pigmentosa patients from India.
Sen P, Srikrupa N, Maitra P, Srilekha S, Porkodi P, Gnanasekaran H, Bhende M, Khetan V, Mathavan S, Bhende P, Ratra D, Raman R, Rao C, Sripriya S. Sen P, et al. Indian J Ophthalmol. 2023 Jun;71(6):2512-2520. doi: 10.4103/IJO.IJO_2579_22. Indian J Ophthalmol. 2023. PMID: 37322672 Free PMC article.
PURPOSE: Inherited retinal dystrophies (IRD) are a heterogeneous group of retinal diseases leading to progressive loss of photoreceptors through apoptosis. Retinitis pigmentosa (RP) is considered the most common form of IRD. Panel-based testing in RP has proven effe …
PURPOSE: Inherited retinal dystrophies (IRD) are a heterogeneous group of retinal diseases leading to progressive loss of photoreceptors thr …
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.
Humphries P, Farrar GJ, Kenna P, McWilliam P. Humphries P, et al. Clin Genet. 1990 Jul;38(1):1-13. doi: 10.1111/j.1399-0004.1990.tb03541.x. Clin Genet. 1990. PMID: 2201466 Review.
Retinitis pigmentosa (RP) is an hereditary degenerative disease of the retina and a major cause of visual impairment, prevalence estimates ranging from 1 in 3000 to 1 in 7000. ...Extensive genetic heterogeneity thus exists in the autosomal dominant form of this dise …
Retinitis pigmentosa (RP) is an hereditary degenerative disease of the retina and a major cause of visual impairment, prevalen …
Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity.
Obuća M, Cvačková Z, Kubovčiak J, Kolář M, Staněk D. Obuća M, et al. PLoS One. 2022 Apr 6;17(4):e0265742. doi: 10.1371/journal.pone.0265742. eCollection 2022. PLoS One. 2022. PMID: 35385551 Free PMC article.
Retinitis pigmentosa (RP) is a hereditary disease affecting tens of thousands of people world-wide. ...We further downregulated DHX38 and monitored changes in splicing. We observed only minor perturbations of general splicing but detected modulation of ~70 …
Retinitis pigmentosa (RP) is a hereditary disease affecting tens of thousands of people world-wide. ...We further downregulate …
95 results