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Quoted phrase not found in phrase index: "Retinitis pigmentosa 64"
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USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa.
Zhu T, Chen DF, Wang L, Wu S, Wei X, Li H, Jin ZB, Sui R. Zhu T, et al. Br J Ophthalmol. 2021 May;105(5):694-703. doi: 10.1136/bjophthalmol-2019-315786. Epub 2020 Jul 16. Br J Ophthalmol. 2021. PMID: 32675063
AIMS: To reveal the Usher syndrome type IIA (USH2A) gene variant profile in a large cohort of Chinese patients with non-syndromic retinitis pigmentosa (RP) or Usher syndrome type II (USH2) and to explore the genotype-phenotype correlation. ...The most common variant …
AIMS: To reveal the Usher syndrome type IIA (USH2A) gene variant profile in a large cohort of Chinese patients with non-syndromic retinit …
Thicknesses of the retina and choroid in children with retinitis pigmentosa.
Li C, Peng C, Zhang C, Li N. Li C, et al. BMC Ophthalmol. 2023 Jan 17;23(1):25. doi: 10.1186/s12886-023-02772-0. BMC Ophthalmol. 2023. PMID: 36650468 Free PMC article.
PURPOSE: To compare the retinal thicknesses (RT) and choroidal thicknesses (CT) in retinitis pigmentosa (RP) children with those of healthy children using enhanced depth imaging (EDI) optical coherence tomography (OCT). ...METHOD: A retrospective analysis was perfor …
PURPOSE: To compare the retinal thicknesses (RT) and choroidal thicknesses (CT) in retinitis pigmentosa (RP) children with tho …
Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review.
Stephenson KAJ, Whelan L, Zhu J, Dockery A, Wynne NC, Cairns RM, Kirk C, Turner J, Duignan ES, O'Byrne JJ, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Invest Ophthalmol Vis Sci. 2023 Jul 3;64(10):23. doi: 10.1167/iovs.64.10.23. Invest Ophthalmol Vis Sci. 2023. PMID: 37466950 Free PMC article.
PURPOSE: Usher syndrome (USH) is a genetically heterogeneous group of autosomal recessive (AR) syndromic inherited retinal degenerations (IRDs) representing 50% of deaf-blindness. All subtypes include retinitis pigmentosa, sensorineural hearing loss, and vestibular …
PURPOSE: Usher syndrome (USH) is a genetically heterogeneous group of autosomal recessive (AR) syndromic inherited retinal degenerations (IR …
Hyperautofluorescent Ring Pattern in Retinitis Pigmentosa: Clinical Implications and Modifications Over Time.
Antropoli A, Arrigo A, Bianco L, Cavallari E, Bandello F, Battaglia Parodi M. Antropoli A, et al. Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):8. doi: 10.1167/iovs.64.12.8. Invest Ophthalmol Vis Sci. 2023. PMID: 37669062 Free PMC article.
PURPOSE: The purpose of this study was to investigate the relation among hyperautofluorescent ring patterns, visual acuity (VA), and optical coherence tomography (OCT) features in patients with retinitis pigmentosa (RP), and to describe its modifications over time. …
PURPOSE: The purpose of this study was to investigate the relation among hyperautofluorescent ring patterns, visual acuity (VA), and optical …
Syndromic Retinitis Pigmentosa: A 15-Patient Study.
Holanda IP, Rim PHH, Rare Genomes Project Consortium, Guaragna MS, Gil-da-Silva-Lopes VL, Steiner CE. Holanda IP, et al. Genes (Basel). 2024 Apr 20;15(4):516. doi: 10.3390/genes15040516. Genes (Basel). 2024. PMID: 38674450 Free PMC article.
Retinitis pigmentosa is a group of genetically determined retinal dystrophies characterized by primary photoreceptor apoptosis and can occur in isolated or syndromic conditions. This study reviewed the clinical data of 15 patients with syndromic retinitis …
Retinitis pigmentosa is a group of genetically determined retinal dystrophies characterized by primary photoreceptor apoptosis …
Association between retinitis pigmentosa and an increased risk of primary angle closure glaucoma: A population-based cohort study.
Hung MC, Chen YY. Hung MC, et al. PLoS One. 2022 Sep 9;17(9):e0274066. doi: 10.1371/journal.pone.0274066. eCollection 2022. PLoS One. 2022. PMID: 36083972 Free PMC article.
BACKGROUND: Retinitis pigmentosa (RP) is the most frequent retinal hereditary dystrophy and result in blindness if progresses. ...According to the univariate Cox regression analysis, the hazard of PACG development was significantly greater in the RP group, with an u …
BACKGROUND: Retinitis pigmentosa (RP) is the most frequent retinal hereditary dystrophy and result in blindness if progresses. …
Metabolic Long-Term Monitoring of Transcorneal Electrical Stimulation in Retinitis Pigmentosa.
Meral N, Zabek O, Camenzind Zuche H, Müller U, Prétot D, Rickmann A, Scholl HPN, Della Volpe Waizel M. Meral N, et al. Ophthalmic Res. 2022;65(1):52-59. doi: 10.1159/000519998. Epub 2021 Oct 4. Ophthalmic Res. 2022. PMID: 34607326 Free article.
INTRODUCTION: Transcorneal electrical stimulation (TES) is a new therapeutical approach for retinitis pigmentosa (RP). With progression of RP, degeneration of photoreceptors results in lower oxygen consumption of the retina. ...RESULTS: After 3Y of TES treatment bot …
INTRODUCTION: Transcorneal electrical stimulation (TES) is a new therapeutical approach for retinitis pigmentosa (RP). With pr …
Long-term Outcomes of Cataract Surgery in Patients with Retinitis Pigmentosa.
Nakamura S, Fujiwara K, Yoshida N, Murakami Y, Shimokawa S, Koyanagi Y, Ikeda Y, Sonoda KH. Nakamura S, et al. Ophthalmol Retina. 2022 Apr;6(4):268-272. doi: 10.1016/j.oret.2021.12.010. Epub 2021 Dec 16. Ophthalmol Retina. 2022. PMID: 34923176
PURPOSE: To investigate the long-term outcomes of cataract surgery in patients with retinitis pigmentosa (RP). DESIGN: Retrospective, observational study. ...RESULTS: Cataract surgery was performed in 96 eyes, with an average follow-up period of 5.8 2.4 years. The m …
PURPOSE: To investigate the long-term outcomes of cataract surgery in patients with retinitis pigmentosa (RP). DESIGN: Retrosp …
Inherited retinal diseases are the most common cause of blindness in the working-age population in Australia.
Heath Jeffery RC, Mukhtar SA, McAllister IL, Morgan WH, Mackey DA, Chen FK. Heath Jeffery RC, et al. Ophthalmic Genet. 2021 Aug;42(4):431-439. doi: 10.1080/13816810.2021.1913610. Epub 2021 May 3. Ophthalmic Genet. 2021. PMID: 33939573 Free PMC article.
Low-vision or blindness-only (20/200 or 20) certificates issued to children (0-15 years), working-age (16-64 years) and older-age (65 and older) adults were assessed. Sex and age distributions were examined for the top 20 reasons for certification. ...The top three phenoty …
Low-vision or blindness-only (20/200 or 20) certificates issued to children (0-15 years), working-age (16-64 years) and older-age (65 …
95 results