Three-Year Follow-Up of Results of Intraocular Lens Fixation in Patients with Retinitis Pigmentosa by Gen Miura, Takayuki Baba

Subjects: “…retinitis pigmentosa…”
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Aberrant dolichol chain lengths as biomarkers for retinitis pigmentosa caused by impaired dolichol biosynthesis by Rong Wen, Byron L. Lam, Ziqiang Guan

“…We observed a characteristic shortening of plasma and urinary dolichols in retinitis pigmentosa (RP) patients carrying K42E and T206A mutations in the dehydrodolichol diphosphate synthase (DHDDS) gene, using liquid chromatography-mass spectrometry. …”
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Retinitis Pigmentosa and Polydactyly in a Patient with a Heterozygous Mutation on the BBS1 Gene by Guardiola G, Ramos F, Izquierdo N

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Management of Cystoid Macular Edema in Retinitis Pigmentosa: A Systematic Review and Meta-Analysis by Chen Chen, Chen Chen, Chen Chen, Xia Liu, Xia Liu, Xia Liu, Xiaoyan Peng, Xiaoyan Peng

Subjects: “…retinitis pigmentosa…”
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Genotypic and phenotypic profiles of EYS gene-related retinitis pigmentosa: a retrospective study by Ragkit Suvannaboon, Aulia Rahmi Pawestri, Worapoj Jinda, Aekkachai Tuekprakhon, Adisak Trinavarat, La-ongsri Atchaneeyasakul

“…Abstract Retinitis pigmentosa (RP) affects 1:5000 individuals worldwide. …”
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Systematic review and meta-synthesis of coping with retinitis pigmentosa: implications for improving quality of life by Gulcan Garip, Atiya Kamal

“…Abstract Background Retinitis pigmentosa (RP) are a group of incurable and inherited eye conditions, and the leading cause of inherited blindness in people under the age of 60. …”
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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa by Béatrice Bocquet, Caroline Borday, Nejla Erkilic, Daria Mamaeva, Alicia Donval, Christel Masson, Karine Parain, Karolina Kaminska, Mathieu Quinodoz, Irene Perea-Romero, Gema Garcia-Garcia, Carla Jimenez-Medina, Hassan Boukhaddaoui, Arthur Coget, Nicolas Leboucq, Giacomo Calzetti, Stefano Gandolfi, Antonio Percesepe, Valeria Barili, Vera Uliana, Marco Delsante, Francesca Bozzetti, Hendrik P.N. Scholl, Marta Corton, Carmen Ayuso, Jose M. Millan, Carlo Rivolta, Isabelle Meunier, Muriel Perron, Vasiliki Kalatzis

“…Retinitis pigmentosa (RP) is the most common inherited retinal disease (IRD) and is characterized by photoreceptor degeneration and progressive vision loss. …”
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Patient-Specific Retinal Organoids Recapitulate Disease Features of Late-Onset Retinitis Pigmentosa by Mei-Ling Gao, Mei-Ling Gao, Xin-Lan Lei, Xin-Lan Lei, Fang Han, Fang Han, Kai-Wen He, Kai-Wen He, Si-Qian Jin, Si-Qian Jin, You-You Zhang, You-You Zhang, Zi-Bing Jin, Zi-Bing Jin

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Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients by Yong Liu, Shao Jun Chen, Shi Ying Li, Ling Hui Qu, Xiao Hong Meng, Yi Wang, Hai Wei Xu, Zhi Qing Liang, Zheng Qin Yin

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℮-conome: an automated tissue counting platform of cone photoreceptors for rodent models of retinitis pigmentosa by Clérin Emmanuelle, Wicker Nicolas, Mohand-Saïd Saddek, Poch Olivier, Sahel José-Alain, Léveillard Thierry

“…<p>Abstract</p> <p>Background</p> <p>Retinitis pigmentosa is characterized by the sequential loss of rod and cone photoreceptors. …”
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Post-Cataract Surgery Visual Disturbance in a Retinitis Pigmentosa Patient with Asteroid Hyalosis by Yoko Jingami, Atsushi Otani, Hiroshi Kojima, Yukiko Makiyama, Nagahisa Yoshimura

Subjects: “…Retinitis pigmentosa…”
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Altered antioxidant-oxidant status in the aqueous humor and peripheral blood of patients with retinitis pigmentosa. by Cristina Martínez-Fernández de la Cámara, David Salom, Ma Dolores Sequedo, David Hervás, Cristina Marín-Lambíes, Elena Aller, Teresa Jaijo, Manuel Díaz-Llopis, José María Millán, Regina Rodrigo

“…Retinitis Pigmentosa is a common form of hereditary retinal degeneration constituting the largest Mendelian genetic cause of blindness in the developed world. …”
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A novel mutation of RPGR in a Chinese family with X-linked retinitis pigmentosa by Hui-Hui Sun, Jing-Cong Zhao, Su-Ling Yang, Jin-Dou Shi, Yun-Shuo Wei, Jian-Cang Wang, Feng Gu, Lu Chen

Subjects: “…x-linked retinitis pigmentosa…”
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Retinal Vascular Degeneration in the Transgenic P23H Rat Model of Retinitis Pigmentosa by Laura Fernández-Sánchez, Gema Esquiva, Isabel Pinilla, Isabel Pinilla, Pedro Lax, Nicolás Cuenca, Nicolás Cuenca

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A New Preclinical Model of Retinitis Pigmentosa Due to Pde6g Deficiency by Michelle Carmen Jentzsch, PhD, Stephen H. Tsang, MD, PhD, Susanne Friederike Koch, PhD

Subjects: “…Retinitis pigmentosa…”
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The qualitative assessment of optical coherence tomography and the central retinal sensitivity in patients with retinitis pigmentosa. by Aiko Hara, Mitsuru Nakazawa, Masaaki Saito, Yukihiko Suzuki

“…PURPOSE:To analyze the relationships between qualitative and quantitative parameters of spectral-domain optical coherence tomography (SD-OCT) and the central retinal sensitivity in patients with retinitis pigmentosa (RP). MATERIALS AND METHODS:Ninety-three eyes of 93 patients were finally enrolled, with a median age (quartile) of 58 (24.5) years. …”
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Clinical significance of chromatic pupillometry in evaluating visual function in blind patients with retinitis pigmentosa by ZHAO He, WANG Hao, WENG Chuanhuang

“…Objective To study the feasibility and effectiveness of quantitative evaluation of retinal function in blind patients with retinitis pigmentosa (RP) by chromatic pupillometry. Methods A total of 46 blind RP patients (81 eyes) who met the legal blindness standard admitted in our department from January 2022 to December 2022 were recruited in this study.According to their best-corrected visual acuity, they were divided into the no form perception (NFP) group, faint form perception (FFP) group, and form perception (FP) group.Another 18 healthy volunteers (18 eyes) were enrolled as controls.The subjects received routine ophthalmic examinations such as color fundus photography, optical coherence tomography (OCT), fundus autofluorescence (FAF), and flash visual evoked potential (FVEP).The thickness of the outer nuclear layer of OCT, vertical diameter of the FAF high fluorescence area, and amplitude of FVEP P2 were collected.Then chromatic pupillometry was performed.The light stimulation mode of low-intensity blue light was conducted to activate rods, and of high-intensity red light to activate cones.The evaluation indexes included transient pupil construction amplitude (TPCA), latency, maximal contraction velocity (MCV), and contraction duration. …”
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Quantification of Macular Microvascular Changes in Retinitis Pigmentosa Using Optical Coherence Tomography Angiography by AttaAllah HR, Mohamed AAM, Hamid MA

Subjects: “…• retinitis pigmentosa • oct angiography • macular microvasculature…”
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Importance of two-dimensional gaze analyses in the assessment of reading performance in patients with retinitis pigmentosa. by Masako Yoshida, Akitoshi Seiyama

“…Reading difficulties in patients with retinitis pigmentosa result from impaired eye movement directionality. …”
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Comparing the Variation of Time and Frequency Components of Electroretinogram in Patients with Retinitis Pigmentosa and Healthy Individuals by Samira Ebdali, Bijan Hashemi, Ebrahim Jafarzadehpour

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