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Quoted phrase not found in phrase index: "Retinitis pigmentosa 90"
Page 1
Artificial Intelligence for Screening of Multiple Retinal and Optic Nerve Diseases.
Dong L, He W, Zhang R, Ge Z, Wang YX, Zhou J, Xu J, Shao L, Wang Q, Yan Y, Xie Y, Fang L, Wang H, Wang Y, Zhu X, Wang J, Zhang C, Wang H, Wang Y, Chen R, Wan Q, Yang J, Zhou W, Li H, Yao X, Yang Z, Xiong J, Wang X, Huang Y, Chen Y, Wang Z, Rong C, Gao J, Zhang H, Wu S, Jonas JB, Wei WB. Dong L, et al. JAMA Netw Open. 2022 May 2;5(5):e229960. doi: 10.1001/jamanetworkopen.2022.9960. JAMA Netw Open. 2022. PMID: 35503220 Free PMC article.
Compared with retinal specialists, RAIDS achieved a higher sensitivity for detection of any retinal abnormality (RAIDS, 91.7% [95% CI, 90.6%-92.8%]; certified ophthalmologists, 83.7% [95% CI, 82.1%-85.1%]; junior retinal specialists, 86.4% [95% CI, 84.9%-87.7%]; and senior …
Compared with retinal specialists, RAIDS achieved a higher sensitivity for detection of any retinal abnormality (RAIDS, 91.7% [95% CI, 90 …
Genetic dissection of non-syndromic retinitis pigmentosa.
Bhardwaj A, Yadav A, Yadav M, Tanwar M. Bhardwaj A, et al. Indian J Ophthalmol. 2022 Jul;70(7):2355-2385. doi: 10.4103/ijo.IJO_46_22. Indian J Ophthalmol. 2022. PMID: 35791117 Free PMC article. Review.
Retinitis pigmentosa (RP) belongs to a group of pigmentary retinopathies. ...In this review, we are going to focus on the genetic heterogeneity of this disease, which is provided by various inheritance patterns, numerosity of variations and inter-/intra-familial var …
Retinitis pigmentosa (RP) belongs to a group of pigmentary retinopathies. ...In this review, we are going to focus on the gene …
Clinical and genetic investigations in Chinese families with retinitis pigmentosa.
Chen L, Wang N, Lai M, Hou F, He J, Fan X, Yao X, Wang R. Chen L, et al. Exp Biol Med (Maywood). 2022 Jun;247(12):1030-1038. doi: 10.1177/15353702221085711. Epub 2022 Apr 11. Exp Biol Med (Maywood). 2022. PMID: 35410501 Free PMC article.
To describe clinical and genetic characteristics in a series of Chinese patients with non-syndromic retinitis pigmentosa, a total of 20 unrelated Chinese pedigrees with non-syndromic retinitis pigmentosa were evaluated. ...These data will help with rap …
To describe clinical and genetic characteristics in a series of Chinese patients with non-syndromic retinitis pigmentosa, a to …
Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds.
Bunel M, Chaudieu G, Hamel C, Lagoutte L, Manes G, Botherel N, Brabet P, Pilorge P, André C, Quignon P. Bunel M, et al. Hum Genet. 2019 May;138(5):441-453. doi: 10.1007/s00439-019-01999-6. Epub 2019 Mar 23. Hum Genet. 2019. PMID: 30904946 Review.
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal disorders eventually leading to blindness with different ages of onset, progression and severity. Human RP, first characterized by the progressive degeneration of rod photoreceptor cells, shows …
Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal disorders eventually leading to blindness with differe …
Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial.
Kuehlewein L, Zobor D, Andreasson SO, Ayuso C, Banfi S, Bocquet B, Bernd AS, Biskup S, Boon CJF, Downes SM, Fischer MD, Holz FG, Kellner U, Leroy BP, Meunier I, Nasser F, Rosenberg T, Rudolph G, Stingl K, Thiadens AAHJ, Wilhelm B, Wissinger B, Zrenner E, Kohl S, Weisschuh N; RD-CURE Consortium. Kuehlewein L, et al. JAMA Ophthalmol. 2020 Dec 1;138(12):1241-1250. doi: 10.1001/jamaophthalmol.2020.4206. JAMA Ophthalmol. 2020. PMID: 33057649 Free PMC article.
OBJECTIVE: To assess clinical features, genetic findings, and genotype-phenotype correlations in patients with retinitis pigmentosa (RP) associated with biallelic sequence variations in the PDE6A gene in preparation for a gene supplementation trial. DESIGN, SETTING, …
OBJECTIVE: To assess clinical features, genetic findings, and genotype-phenotype correlations in patients with retinitis pigmentos …
Clinical Presentation and Demographic Distribution of Retinitis Pigmentosa in India and Implications for Potential Treatments: Electronic Medical Records Driven Big Data Analytics: Report I.
Parameswarappa DC, Das AV, Dave VP, Agarwal K, Natarajan R, Jalali S. Parameswarappa DC, et al. Semin Ophthalmol. 2022 Apr 3;37(3):284-290. doi: 10.1080/08820538.2021.1957126. Epub 2021 Aug 17. Semin Ophthalmol. 2022. PMID: 34404308
AimTo describe the clinical presentation and demographic distribution of retinitis pigmentosa in patients presenting to a multi-tier ophthalmology hospital network in India and implications for potential treatments.DesignCross-sectional hospital-based study.MethodsT …
AimTo describe the clinical presentation and demographic distribution of retinitis pigmentosa in patients presenting to a mult …
No Light Perception Vision in Neuro-Ophthalmology Practice.
Garg A, Margolin E, Micieli JA. Garg A, et al. J Neuroophthalmol. 2022 Mar 1;42(1):e225-e229. doi: 10.1097/WNO.0000000000001340. Epub 2021 Jul 27. J Neuroophthalmol. 2022. PMID: 34334760
Other diagnoses included optic neuritis (ON) (11 patients), infiltrative optic neuropathies (8), posterior ischemic optic neuropathy (7), nonarteritic anterior ischemic optic neuropathy (4), arteritic anterior ischemic optic neuropathy (3), ophthalmic artery occlusion (3), nonorg …
Other diagnoses included optic neuritis (ON) (11 patients), infiltrative optic neuropathies (8), posterior ischemic optic neuropathy (7), no …
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher Syndrome.
Daich Varela M, Wong SW, Kiray G, Schlottmann PG, Arno G, Shams ANA, Mahroo OA, Webster AR, AlTalbishi A, Michaelides M. Daich Varela M, et al. Am J Ophthalmol. 2023 Dec;256:186-195. doi: 10.1016/j.ajo.2023.06.026. Epub 2023 Jul 7. Am J Ophthalmol. 2023. PMID: 37422204 Free article.
Visual symptom onset was at 17.0 7.7 years of age (range: 6-32 years), with 13 patients noticing problems before the age of 16. At baseline, 90% of patients had no or mild visual impairment. The most frequent retinal features were a hyperautofluorescent ring at the posteri …
Visual symptom onset was at 17.0 7.7 years of age (range: 6-32 years), with 13 patients noticing problems before the age of 16. At baseline, …
Cutaneous findings in Bardet-Biedl syndrome.
Haws RM, McIntee TJ, Green CB. Haws RM, et al. Int J Dermatol. 2019 Oct;58(10):1160-1164. doi: 10.1111/ijd.14412. Epub 2019 Feb 20. Int J Dermatol. 2019. PMID: 30790276
Obesity, a cardinal feature of BBS, was present in the majority of subjects (90.3%) and was accompanied by known obesity-related dermatologic disorders. ...
Obesity, a cardinal feature of BBS, was present in the majority of subjects (90.3%) and was accompanied by known obesity-related derm …
Genotypes and clinical features of RHO-associated retinitis pigmentosa in a Japanese population.
Tsutsui S, Murakami Y, Fujiwara K, Koyanagi Y, Akiyama M, Takeda A, Ikeda Y, Sonoda KH. Tsutsui S, et al. Jpn J Ophthalmol. 2024 Jan;68(1):1-11. doi: 10.1007/s10384-023-01036-0. Epub 2023 Dec 9. Jpn J Ophthalmol. 2024. PMID: 38070066
PURPOSE: To report the genotypes and clinical features of RHO-associated retinitis pigmentosa (RHO-RP) in the Kyushu region of Japan. STUDY DESIGN: Retrospective, single-center study. ...
PURPOSE: To report the genotypes and clinical features of RHO-associated retinitis pigmentosa (RHO-RP) in the Kyushu region of …
94 results