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Mutation Report

Reversal of cystoid macular edema in gyrate atrophy patients

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Pages 549-554 | Received 27 Dec 2016, Accepted 26 Feb 2017, Published online: 07 Apr 2017

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Mariana Matioli da Palma, Cristy Ku, Austin D. Igelman, Amanda Burr, Liliya Shevchenko Sutherland, Celide Koerner, David Valle, Mark E. Pennesi & Paul Yang. (2023) A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease. Ophthalmic Genetics 44:2, pages 191-197.
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Masood Naseripour, Sara Hemmati, Samira Chaibakhsh, Arzhang Gordiz, Leila Miri & Fatemeh Abdi. (2022) Cystoid macular oedema without leakage in fluorescein angiography: a literature review. Eye 37:8, pages 1519-1526.
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Sang Jin Kim. 2022. Inherited Retinal Disease. Inherited Retinal Disease 221 227 .
Wenxue Guan, Ge Wang, Feng Hu & Xiaoyan Peng. (2021) Partial regression of foveoschisis following vitamin B6 supplementary therapy for gyrate atrophy in a Chinese girl. BMC Ophthalmology 21:1.
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Berith M. Balfoort, Mark J.N. Buijs, Anneloor L.M.A. ten Asbroek, Arthur A.B. Bergen, Camiel J.F. Boon, Elise A. Ferreira, Riekelt H. Houtkooper, Margreet A.E.M. Wagenmakers, Ronald J.A. Wanders, Hans R. Waterham, Corrie Timmer, Clara D. van Karnebeek & Marion M. Brands. (2021) A review of treatment modalities in gyrate atrophy of the choroid and retina (GACR). Molecular Genetics and Metabolism 134:1-2, pages 96-116.
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Riccardo Montioli, Giada Sgaravizzi, Maria Andrea Desbats, Silvia Grottelli, Carla Borri Voltattorni, Leonardo Salviati & Barbara Cellini. (2021) Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina. Frontiers in Molecular Biosciences 8.
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Ahmad M. Mansour, Ayman G. Elnahry, Koushik Tripathy, Robert E. Foster, Carl-Jo Mehanna, Raval Vishal, Cemal Çavdarlı, Alessandro Arrigo & Maurizio Battaglia Parodi. (2020) Analysis of optical coherence angiography in cystoid macular oedema associated with gyrate atrophy. Eye 35:6, pages 1766-1774.
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Myron Yanoff & Joseph W. Sassani. 2020. Ocular Pathology. Ocular Pathology 357 379.e5 .
Junting Huang, Jiewen Fu, Shangyi Fu, Lisha Yang, Kailai Nie, Chengxia Duan, Jingliang Cheng, Yumei Li, Hongbin Lv, Rui Chen, Longqian Liu & Junjiang Fu. (2019) Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant. British Journal of Ophthalmology 103:3, pages 428-435.
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Imène Zhioua Braham, Imen Ammous, Rim Maalej, Majdi Boukari, Ilhem Mili Boussen, Khalil Errais & Raja Zhioua. (2018) Multimodal imaging of foveoschisis and macular pseudohole associated with gyrate atrophy: a family report. BMC Ophthalmology 18:1.
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Adrian Dockery, Kirk Stephenson, David Keegan, Niamh Wynne, Giuliana Silvestri, Peter Humphries, Paul F. Kenna, Matthew Carrigan & G. Jane Farrar. (2017) Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations. Genes 8:11, pages 304.
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