Bilateral presumed astrocytic hamartomas in a patient with retinitis pigmentosa by Kinori M, Moroz I, Rotenstreich Y, Yonath H, Fabian ID, Vishnevskia-Dai V

“…An association between astrocytic hamartomas and retinitis pigmentosa (RP) has been described previously, but controversy still exists regarding the precise nature of these lesions in RP patients. …”
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New In Vitro Cellular Model for Molecular Studies of Retinitis Pigmentosa by Li Huang, Meltem Kutluer, Elisa Adani, Antonella Comitato, Valeria Marigo

“…Retinitis pigmentosa (RP) is an inherited form of retinal degeneration characterized by primary rod photoreceptor cell death followed by cone loss. …”
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Possible Role of Insulin-Degrading Enzyme in the Physiopathology of Retinitis Pigmentosa by Alonso Sánchez-Cruz, María D. Hernández-Fuentes, Cayetana Murillo-Gómez, Enrique J. de la Rosa, Catalina Hernández-Sánchez

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SNRNP200 Mutations Cause Autosomal Dominant Retinitis Pigmentosa by Tao Zhang, Tao Zhang, Jingshan Bai, Jingshan Bai, Xinyi Zhang, Xinyi Zhang, Xiaowei Zheng, Xiaowei Zheng, Nan Lu, Zhongyin Liang, Ling Lin, Ling Lin, Yongsong Chen, Yongsong Chen

Subjects: “…retinitis pigmentosa…”
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Unusual Association of Inverse Retinitis Pigmentosa, Scleromalacia, and Neovascular Glaucoma by Ayşe Gül Koçak Altıntaş, Çağrı İlhan, Mehmet Çıtırık

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Retinal Pigment Epithelium Remodeling in Mouse Models of Retinitis Pigmentosa by Debora Napoli, Martina Biagioni, Federico Billeri, Beatrice Di Marco, Noemi Orsini, Elena Novelli, Enrica Strettoi

Subjects: “…retinitis pigmentosa…”
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Modeling retinitis pigmentosa through patient-derived retinal organoids by Yan-Ping Li, Wen-Li Deng, Zi-Bing Jin

“…In this protocol, we successfully established 3D retinae from patient-derived hiPSCs and built the retinitis pigmentosa model in vitro. Moreover, mutation in the retinitis pigmentosa GTPase regulator (RPGR) gene was corrected by CRISPR-Cas9 gene editing, which rescued the structure and function of the 3D retinae.For complete details on the use and execution of this protocol, please refer to Deng et al. (2018).…”
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Anatomical and functional correlates of cystic macular edema in retinitis pigmentosa. by Adam Ruff, Alangoya Tezel, Tongalp H Tezel

“…Cystoid macular edema (CME) is a major cause of central visual deterioration in retinitis pigmentosa. The exact reason for CME and its prognostic significance in this patient population is unknown. …”
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Retinitis pigmentosa with unilateral choroidal coloboma: A rare association by Pallavi Agrawal, Priyanka Suresh Karande, Leena Vadhel, Abidi Naheed

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Retinitis Pigmentosa Associated with Vasoproliferative Tumors and Coats-like Fundus by Fariba Ghassemi, Marjan Akbari-Kamrani

Subjects: “…Capillary Nonperfusion; Coats Disease; Retinitis Pigmentosa; Telangiectasia; Vasoproliferative Tumors…”
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Clinical and Electrophysiological Report of a Unilateral Retinitis Pigmentosa Case by Sedaghat MR, Askari S.A, Afshar R

Subjects: “…Electro-oculography Electro-retinography Unilateral retinitis pigmentosa…”
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The role of mislocalized phototransduction in photoreceptor cell death of retinitis pigmentosa. by Takeshi Nakao, Motokazu Tsujikawa, Shoji Notomi, Yasuhiro Ikeda, Kohji Nishida

“…Most of inherited retinal diseases such as retinitis pigmentosa (RP) cause photoreceptor cell death resulting in blindness. …”
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Electroretinography and OCT angiography of the retina and optic nerve in retinitis pigmentosa by V. . Zolnikova, D. V. Levina, T. D. Okhotsimskaya, V. A. Fadeeva, I. V. Egorova, E. V. Rogatina, E. A. Eremeeva, O. N. Demenkova, S. Yu. Rogova

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Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutants by Birgit Ploier, Lydia N. Caro, Takefumi Morizumi, Kalpana Pandey, Jillian N. Pearring, Michael A. Goren, Silvia C. Finnemann, Johannes Graumann, Vadim Y. Arshavsky, Jeremy S. Dittman, Oliver P. Ernst, Anant K. Menon

“…Retinitis pigmentosa is often caused by mutations that affect the activity or transport of rhodopsin, but some mutations cause disease even though an apparently functional protein is produced. …”
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A pedigree with retinitis pigmentosa and its concomitant ophthalmic diseases by Hong-Dou Luo, Shao-Nan Pei, Ai-Jia Wang, Xue-Qing Yu, Hai-Jian Hu, Ling Zeng, Fei-Fei Wang, Ming Jin, Xu Zhang

Subjects: “…retinitis pigmentosa…”
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<i>Weill-Marchesani syndrome</i> associated with retinitis pigmentosa by Jethani Jitendra, Mishra Anurag, Shetty Shashikant, Vijayalakshmi P

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Metabolic Deregulation of the Blood-Outer Retinal Barrier in Retinitis Pigmentosa by Wei Wang, Ashwini Kini, Yekai Wang, Tingting Liu, Yao Chen, Eric Vukmanic, Douglas Emery, Yongqing Liu, Xiaoqin Lu, Lei Jin, San Joon Lee, Patrick Scott, Xiao Liu, Kevin Dean, Qingxian Lu, Enzo Fortuny, Robert James, Henry J. Kaplan, Jianhai Du, Douglas C. Dean

“…Summary: Retinitis pigmentosa (RP) initiates with diminished rod photoreceptor function, causing peripheral and night-time vision loss. …”
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Metabolic transcriptomics dictate responses of cone photoreceptors to retinitis pigmentosa by San Joon Lee, Douglas Emery, Eric Vukmanic, Yekai Wang, Xiaoqin Lu, Wei Wang, Enzo Fortuny, Robert James, Henry J. Kaplan, Yongqing Liu, Jianhai Du, Douglas C. Dean

“…Summary: Most mutations in retinitis pigmentosa (RP) arise in rod photoreceptors, but cone photoreceptors, responsible for high-resolution daylight and color vision, are subsequently affected, causing the most debilitating features of the disease. …”
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Pupil size following dark adaptation in patients with retinitis pigmentosa by A. Berezovsky, S.R. Salomão, D.G. Birch

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Cell Ferroptosis: New Mechanism and New Hope for Retinitis Pigmentosa by Ming Yang, Kwok-Fai So, Wai-Ching Lam, Amy Cheuk Yin Lo

“…Retinitis pigmentosa (RP) is a leading cause of inherited retinal degeneration, with more than 60 gene mutations. …”
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