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Page 1
Asymmetric diabetic retinopathy.
Azad R, Sinha S, Nishant P. Azad R, et al. Indian J Ophthalmol. 2021 Nov;69(11):3026-3034. doi: 10.4103/ijo.IJO_1525_21. Indian J Ophthalmol. 2021. PMID: 34708738 Free PMC article. Review.
This thematic synthesis based on an iterative literature review conducted in Medline and Google Scholar pertaining to diabetes with coexistent asymmetry of retinopathy included 45 original articles, 21 case reports and series, and 18 review articles from 1965 to 2020. ...A …
This thematic synthesis based on an iterative literature review conducted in Medline and Google Scholar pertaining to diabetes with coexiste …
Retinitis pigmentosa.
Hartong DT, Berson EL, Dryja TP. Hartong DT, et al. Lancet. 2006 Nov 18;368(9549):1795-809. doi: 10.1016/S0140-6736(06)69740-7. Lancet. 2006. PMID: 17113430 Review.
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vis …
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses …
Retinitis pigmentosa.
Hamel C. Hamel C. Orphanet J Rare Dis. 2006 Oct 11;1:40. doi: 10.1186/1750-1172-1-40. Orphanet J Rare Dis. 2006. PMID: 17032466 Free PMC article. Review.
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal pigment deposits visible on fundus examination. ...RP is usually non syndromic but there are also many syndromic forms, the most frequent be …
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and characterized by retinal …
Microglia in the Retina: Roles in Development, Maturity, and Disease.
Silverman SM, Wong WT. Silverman SM, et al. Annu Rev Vis Sci. 2018 Sep 15;4:45-77. doi: 10.1146/annurev-vision-091517-034425. Epub 2018 May 31. Annu Rev Vis Sci. 2018. PMID: 29852094 Review.
Under pathological conditions, retinal microglia participate in potentiating neurodegeneration in diseases such as glaucoma, retinitis pigmentosa, and age-related neurodegeneration by producing proinflammatory neurotoxic cytokines and removing living neurons via pha …
Under pathological conditions, retinal microglia participate in potentiating neurodegeneration in diseases such as glaucoma, retinitis …
Nerve Growth Factor: Early Studies and Recent Clinical Trials.
Rocco ML, Soligo M, Manni L, Aloe L. Rocco ML, et al. Curr Neuropharmacol. 2018;16(10):1455-1465. doi: 10.2174/1570159X16666180412092859. Curr Neuropharmacol. 2018. PMID: 29651949 Free PMC article. Review.
These studies revealed that NGF possesses important therapeutic properties, after topical administration, on human cutaneous pressure ulcer, corneal ulcers, glaucoma, retinal maculopathy, Retinitis Pigmentosa and in pediatric optic gliomas and brain traumas. ...
These studies revealed that NGF possesses important therapeutic properties, after topical administration, on human cutaneous pressure ulcer, …
Nephronophthisis.
Salomon R, Saunier S, Niaudet P. Salomon R, et al. Pediatr Nephrol. 2009 Dec;24(12):2333-44. doi: 10.1007/s00467-008-0840-z. Epub 2008 Jul 8. Pediatr Nephrol. 2009. PMID: 18607645 Free PMC article. Review.
The infantile form is characterized by cortical microcysts and progression to end-stage renal failure before 5 years of age. Some children present with extrarenal symptoms: retinitis pigmentosa (Senior-Loken syndrome), mental retardation, cerebellar ataxia, bone ano …
The infantile form is characterized by cortical microcysts and progression to end-stage renal failure before 5 years of age. Some children p …
Posterior staphyloma in pathologic myopia.
Ohno-Matsui K, Jonas JB. Ohno-Matsui K, et al. Prog Retin Eye Res. 2019 May;70:99-109. doi: 10.1016/j.preteyeres.2018.12.001. Epub 2018 Dec 8. Prog Retin Eye Res. 2019. PMID: 30537538 Review.
Besides in highly myopic eyes, a posterior staphyloma can be found in non-highly myopic eyes in association with retinitis pigmentosa or localized defects of Bruch's membrane in the cases of which it is not associated with a marked choroidal thinning. ...
Besides in highly myopic eyes, a posterior staphyloma can be found in non-highly myopic eyes in association with retinitis pigment …
Bestrophin 1 and retinal disease.
Johnson AA, Guziewicz KE, Lee CJ, Kalathur RC, Pulido JS, Marmorstein LY, Marmorstein AD. Johnson AA, et al. Prog Retin Eye Res. 2017 May;58:45-69. doi: 10.1016/j.preteyeres.2017.01.006. Epub 2017 Jan 30. Prog Retin Eye Res. 2017. PMID: 28153808 Free PMC article. Review.
These five associated diseases are: Best vitelliform macular dystrophy, autosomal recessive bestrophinopathy, adult-onset vitelliform macular dystrophy, autosomal dominant vitreoretinochoroidopathy, and retinitis pigmentosa. The most common of these is Best vitellif …
These five associated diseases are: Best vitelliform macular dystrophy, autosomal recessive bestrophinopathy, adult-onset vitelliform macula …
Optogenetic approaches to retinal prosthesis.
Barrett JM, Berlinguer-Palmini R, Degenaar P. Barrett JM, et al. Vis Neurosci. 2014 Sep;31(4-5):345-54. doi: 10.1017/S0952523814000212. Epub 2014 Aug 6. Vis Neurosci. 2014. PMID: 25100257 Free PMC article. Review.
The concept of visual restoration via retinal prosthesis arguably started in 1992 with the discovery that some of the retinal cells were still intact in those with the retinitis pigmentosa disease. Two decades later, the first commercially available devices have the …
The concept of visual restoration via retinal prosthesis arguably started in 1992 with the discovery that some of the retinal cells were sti …
[Retinitis pigmentosa - a review. Pathogenesis, guidelines for diagnostics and perspectives].
Zobor D, Zrenner E. Zobor D, et al. Ophthalmologe. 2012 May;109(5):501-14;quiz 515. doi: 10.1007/s00347-012-2555-6. Ophthalmologe. 2012. PMID: 22581051 Review. German.
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of hereditary retinal disorders, being one of the most common types of retinal degeneration with a prevalence of 1:4,000. More than 45 genes have so far been associated with RP and …
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of hereditary retinal disorders, being one of th …
31 results