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pro vyhledávání: '"X-linked juvenile retinoschisis"'
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Publikováno v:
Diagnostics, Vol 13, Iss 19, p 3035 (2023)
X-linked juvenile retinoschisis (XLRS) is an inherited disorder characterized by retinal schisis cavities, which can be observed in optical coherence tomography (OCT) images. Monitoring disease progression necessitates the accurate segmentation and q
Externí odkaz:
https://doaj.org/article/8cbcb0c2f12b444c9044fa46b09d3bb3
Publikováno v:
Nigerian Postgraduate Medical Journal, Vol 29, Iss 3, Pp 278-280 (2022)
A 15-year-old boy came to the eye clinic with reduced vision in the left eye of a year's duration and prior trauma. Best-corrected visual acuity was 6/9 and hand movement in both eyes, respectively. The anterior segment examination was essentially no
Externí odkaz:
https://doaj.org/article/f94b9ff8428841ee8931157dc5eeb4c9
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
PurposeTo study the long-term photoreceptor changes and to evaluate the effects of topical application of a carbonic anhydrase inhibitor (CAI) in a mouse model of X-linked retinoschisis (XLRS).MethodsConventional electroretinograms (ERGs) and dark-ad
Externí odkaz:
https://doaj.org/article/2f2ec0219e1141fdba487a73c238017b
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Purpose: X-linked juvenile retinoschisis (XLRS), caused by mutations in the RS1 gene, is an X-linked recessive inherited disease that typically involves both eyes in the first 2 decades of life. Recently, the phenotype heterogeneity of this condition
Externí odkaz:
https://doaj.org/article/05954bb66d08465e94f52925363b1e2b
Autor:
Shih‐Jie Chou, Peng Yang, Qian Ban, Yi‐Ping Yang, Mong‐Lien Wang, Chian‐Shiu Chien, Shih‐Jen Chen, Na Sun, Yazhen Zhu, Hongtao Liu, Wenqiao Hui, Tai‐Chi Lin, Fang Wang, Ryan Yue Zhang, Viet Q. Nguyen, Wenfei Liu, Mengxiang Chen, Steve J. Jonas, Paul S. Weiss, Hsian‐Rong Tseng, Shih‐Hwa Chiou
Publikováno v:
Advanced Science, Vol 7, Iss 10, Pp n/a-n/a (2020)
Abstract The homology‐independent targeted integration (HITI) strategy enables effective CRISPR/Cas9‐mediated knockin of therapeutic genes in nondividing cells in vivo, promising general therapeutic solutions for treating genetic diseases like X
Externí odkaz:
https://doaj.org/article/73b313974d854f8cbb56eec82f8ba8d4
Autor:
Parveen Sen, Ashutosh Agarwal, Pramod Bhende, Lingam Gopal, Muna Bhende, Pukhraj Rishi, Tarun Sharma, Mukesh Jain
Publikováno v:
Indian Journal of Ophthalmology, Vol 66, Iss 12, Pp 1825-1831 (2018)
Purpose: Rhegmatogenous retinal detachment (RRD) is a vision-threatening complication of X-linked juvenile retinoschisis (XLRS). The aim of this study is to report the anatomical and functional outcomes of vitreoretinal surgery for the treatment of R
Externí odkaz:
https://doaj.org/article/f2b2db22091f48bca0efad4c149f9c75
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 47, Iss 5, Pp 302-305 (2017)
X-linked juvenile retinoschisis (XLRS) is an X-linked hereditary retinal dystrophy characterized by splitting of the neurosensory retina. On fundus examination, the macula often has a spoke wheel appearance with foveal cystic lesions, and separation
Externí odkaz:
https://doaj.org/article/f4a81334d0274fd9940d2fed2d29e466
Autor:
Irini Chatziralli, George Theodossiadis, Dimitrios Brouzas, Ioannis Emfietzoglou, Panagiotis Theodossiadis
Publikováno v:
Case Reports in Ophthalmology, Vol 8, Iss 3, Pp 459-464 (2017)
Purpose: We present the evolution of X-linked juvenile retinoschisis (XLRS) in a male patient using optical coherence tomography (OCT) with a long-term follow-up time of 15 years. Case Description: A 10-year-old male patient presented at the Medical
Externí odkaz:
https://doaj.org/article/d1433db04ff145a0ac534907d2b2bc3c
Akademický článek
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