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Quoted phrase not found in phrase index: "Retinitis pigmentosa 58"
Page 1
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.
Gao FJ, Li JK, Chen H, Hu FY, Zhang SH, Qi YH, Xu P, Wang DD, Wang LS, Chang Q, Zhang YJ, Liu W, Li W, Wang M, Chen F, Xu GZ, Wu JH. Gao FJ, et al. Ophthalmology. 2019 Nov;126(11):1549-1556. doi: 10.1016/j.ophtha.2019.04.038. Epub 2019 May 1. Ophthalmology. 2019. PMID: 31054281
PURPOSE: To characterize the genetic landscape of patients with suspected retinitis pigmentosa (RP) in the Chinese population. DESIGN: Cohort study. ...Diagnostic yield was higher among patients in the early-onset subgroup (5 years old, 79.58%) than in the ch …
PURPOSE: To characterize the genetic landscape of patients with suspected retinitis pigmentosa (RP) in the Chinese population. …
IMPG2-Related Maculopathy.
Birtel J, Caswell R, De Silva SR, Herrmann P, Rehman S, Lotery AJ, Mahroo OA, Michaelides M, Webster AR, MacLaren RE, Charbel Issa P. Birtel J, et al. Am J Ophthalmol. 2024 Feb;258:32-42. doi: 10.1016/j.ajo.2023.10.002. Epub 2023 Oct 6. Am J Ophthalmol. 2024. PMID: 37806544
RESULTS: A total of 25 individuals with a mono-allelic IMPG2 variant were included, 5 of whom were relatives of patients with IMPG2-associated retinitis pigmentosa. A distinct maculopathy was present in 17 individuals (median age, 52 years; range, 20-72 years), and …
RESULTS: A total of 25 individuals with a mono-allelic IMPG2 variant were included, 5 of whom were relatives of patients with IMPG2-associat …
Retinitis Pigmentosa and Other Dystrophies.
Mrejen S, Audo I, Bonnel S, Sahel JA. Mrejen S, et al. Dev Ophthalmol. 2017;58:191-201. doi: 10.1159/000455281. Epub 2017 Mar 28. Dev Ophthalmol. 2017. PMID: 28351048
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations characterized by progressive degeneration of rod and cone cells that affects predominantly peripheral visual fields. ...
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal degenerations characterized by progressive degeneratio …
Cataract surgery in retinitis pigmentosa.
Chatterjee S, Agrawal D, Agrawal D, Parchand SM, Sahu A. Chatterjee S, et al. Indian J Ophthalmol. 2021 Jul;69(7):1753-1757. doi: 10.4103/ijo.IJO_2916_20. Indian J Ophthalmol. 2021. PMID: 34146021 Free PMC article.
PURPOSE: The aim of this study was to evaluate visual outcomes of cataract surgery in patients with retinitis pigmentosa. METHODS: This retrospective case series includes a review of the medical records of all patients with retinitis pigmentosa undergo …
PURPOSE: The aim of this study was to evaluate visual outcomes of cataract surgery in patients with retinitis pigmentosa. METH …
Longitudinal Microstructure Changes of the Retina and Choroid in Retinitis Pigmentosa.
Yoon CK, Bae K, Yu HG. Yoon CK, et al. Am J Ophthalmol. 2022 Sep;241:149-159. doi: 10.1016/j.ajo.2022.05.002. Epub 2022 May 9. Am J Ophthalmol. 2022. PMID: 35551907
PURPOSE: To investigate longitudinal changes in the retinal and choroidal microstructure of the macula in patients with retinitis pigmentosa (RP). DESIGN: Retrospective, observational cohort study. ...RESULTS: Significant decreases (median [interquartile range]) in …
PURPOSE: To investigate longitudinal changes in the retinal and choroidal microstructure of the macula in patients with retinitis …
A review of the immunologic findings observed in retinitis pigmentosa.
McMurtrey JJ, Tso MOM. McMurtrey JJ, et al. Surv Ophthalmol. 2018 Nov-Dec;63(6):769-781. doi: 10.1016/j.survophthal.2018.03.002. Epub 2018 Mar 16. Surv Ophthalmol. 2018. PMID: 29551596 Review.
Most patients suffering from retinitis pigmentosa (RP) inherit the disorder; however, the immune-pathologic features associated with this disease have yet to be extensively studied. ...Twenty-one percent to 51% of RP patients display antiretinal antibodies, whereas …
Most patients suffering from retinitis pigmentosa (RP) inherit the disorder; however, the immune-pathologic features associate …
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 …
Vitreo-macular interface disorders in retinitis pigmentosa.
Fragiotta S, Rossi T, Carnevale C, Cutini A, Tricarico S, Casillo L, Scuderi G, Vingolo EM. Fragiotta S, et al. Graefes Arch Clin Exp Ophthalmol. 2019 Oct;257(10):2137-2146. doi: 10.1007/s00417-019-04418-8. Epub 2019 Jul 19. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 31324966
PURPOSE: To investigate the prevalence and progression of vitreo-macular interface disorders (VMID) phenotypes and their natural history in retinitis pigmentosa (RP). METHODS: A total of 257 eyes of 145 RP patients with VMID were retrospectively evaluated. ...
PURPOSE: To investigate the prevalence and progression of vitreo-macular interface disorders (VMID) phenotypes and their natural history in …
Corneal characteristics in patients with retinitis pigmentosa.
Zeki Fikret C, Ucgun NI, Karaca EE, Evren Kemer O. Zeki Fikret C, et al. Photodiagnosis Photodyn Ther. 2023 Jun;42:103554. doi: 10.1016/j.pdpdt.2023.103554. Epub 2023 Apr 6. Photodiagnosis Photodyn Ther. 2023. PMID: 37030435
BACKGROUND: To evaluate corneal topography and specular microscopic findings in patients with retinitis pigmentosa. METHODS: One hundred and two eyes of 51 patients with retinitis pigmentosa and 60 eyes of 30 healty subjects were included in our study. …
BACKGROUND: To evaluate corneal topography and specular microscopic findings in patients with retinitis pigmentosa. METHODS: O …
Hair cortisol level as a molecular biomarker in retinitis pigmentosa patients.
Mateos-Olivares M, Sobas EM, Puertas-Neyra K, Peralta-Ramírez MI, González-Pérez R, Martín-Vallejo J, García-Vázquez C, Coco RM, Pastor JC, Pastor-Idoate S, Usategui-Martín R. Mateos-Olivares M, et al. Exp Eye Res. 2022 Jun;219:109019. doi: 10.1016/j.exer.2022.109019. Epub 2022 Mar 6. Exp Eye Res. 2022. PMID: 35263654 Free article.
PURPOSE: Retinitis pigmentosa (RP) patients commonly experience negative psychological states due to their progressive and unpredictable loss of vision and visual variations related to stress. ...RESULTS: Fifty-two (67%) patients had severe RP and 26 (33%) mild-mode …
PURPOSE: Retinitis pigmentosa (RP) patients commonly experience negative psychological states due to their progressive and unp …
89 results