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Clinical Ophthalmology Volume 9, 2015 - Issue
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Original Research

Radial fundus autofluorescence in the periphery in patients with X-linked retinitis pigmentosa

Ken Ogino1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanCorrespondence[email protected]
,
Maho Oishi1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
,
Akio Oishi1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
,
Satoshi Morooka1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
,
Masako Sugahara1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
,
Norimoto Gotoh1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan;2 Center for Genomic Medicine, Kyoto University, Kyoto, Japan
,
Masafumi Kurimoto3 Department of Ophthalmology, Kyoto Katsura Hospital, Kyoto, Japan
&
Nagahisa Yoshimura1 Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
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Pages 1467-1474 | Published online: 17 Aug 2015

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Grecia Yael Ortiz-Ramirez, Cristina Villanueva-Mendoza, Juan Carlos Zenteno Ruiz, Mariana Reyes & Vianney Cortés-González. (2020) Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene. Ophthalmic Genetics 41:6, pages 625-628.
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Articles from other publishers (12)

João Pedro Marques, Rosa Pinheiro, Ana Luísa Carvalho, Miguel Raimundo, Mário Soares, Pedro Melo, Joaquim Murta, Jorge Saraiva & Rufino Silva. (2022) Genetic spectrum, retinal phenotype, and peripapillary RNFL thickness in RPGR heterozygotes. Graefe's Archive for Clinical and Experimental Ophthalmology 261:3, pages 867-878.
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Danial Roshandel, Tina M. Lamey, Jason Charng, Rachael C. Heath Jeffery, Terri L. McLaren, Jennifer A. Thompson, John N. De Roach, Samuel McLenachan, David A. Mackey & Fred K. Chen. (2023) Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation Carriers . Investigative Opthalmology & Visual Science 64:1, pages 3.
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Alexa L. Li, Shyamanga Borooah & Eric Nudleman. (2022) Multimodal imaging of retinal findings in syndactyly, telecanthus, anogenital, and renal malformations (STAR) syndrome. American Journal of Ophthalmology Case Reports 25, pages 101284.
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Alessia Amato, Alessandro Arrigo, Emanuela Aragona, Maria Pia Manitto, Andrea Saladino, Francesco Bandello & Maurizio Battaglia Parodi. (2021) Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art. Frontiers in Medicine 8.
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Junxing Yang, Lin Zhou, Jiamin Ouyang, Xueshan Xiao, Wenmin Sun, Shiqiang Li & Qingjiong Zhang. (2021) Genotype–Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review. Frontiers in Genetics 12.
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Maria Vittoria Cicinelli, Alessandro Marchese, Alessandro Bordato, Maria Pia Manitto, Francesco Bandello & Maurizio Battaglia Parodi. (2020) Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies. Ophthalmology and Therapy 9:2, pages 249-263.
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Akio Oishi, Manabu Miyata, Shogo Numa, Yuki Otsuka, Maho Oishi & Akitaka Tsujikawa. (2019) Wide-field fundus autofluorescence imaging in patients with hereditary retinal degeneration: a literature review. International Journal of Retina and Vitreous 5:S1.
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Kentaro Kurata, Katsuhiro Hosono, Takaaki Hayashi, Kei Mizobuchi, Satoshi Katagiri, Daisuke Miyamichi, Sachiko Nishina, Miho Sato, Noriyuki Azuma, Tadashi Nakano & Yoshihiro Hotta. (2019) X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers. International Journal of Molecular Sciences 20:6, pages 1518.
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Angelos Kalitzeos, Ranjit Samra, Melissa Kasilian, James J. L. Tee, Margaret Strampe, Christopher Langlo, Andrew R. Webster, Alfredo Dubra, Joseph Carroll & Michel Michaelides. (2019) CELLULAR IMAGING OF THE TAPETAL-LIKE REFLEX IN CARRIERS OF RPGR-ASSOCIATED RETINOPATHY. Retina 39:3, pages 570-580.
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Johannes Birtel, Martin Gliem, Elisabeth Mangold, Philipp L. Müller, Frank G. Holz, Christine Neuhaus, Steffen Lenzner, Diana Zahnleiter, Christian Betz, Tobias Eisenberger, Hanno J. Bolz & Peter Charbel Issa. (2018) Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa. PLOS ONE 13:12, pages e0207958.
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Jesse D. Sengillo, Gabrielle Fridman, Galaxy Y. Cho, Christie Buchovecky & Stephen H. Tsang. (2018) Novel Mutation in Retinitis Pigmentosa GTPase Regulator Gene Causes Primary Ciliary Dyskinesia and Retinitis Pigmentosa. Ophthalmic Surgery, Lasers and Imaging Retina 49:7, pages 548-552.
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Amir H. Hariri, Wei Gui, Ghazala A. Datoo O'Keefe, Michael S. Ip, SriniVas R. Sadda & Michael B. Gorin. (2018) Ultra-Widefield Fundus Autofluorescence Imaging of Patients with Retinitis Pigmentosa. Ophthalmology Retina 2:7, pages 735-745.
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