Citations (32)
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Kent W. Small. (2023) Comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy”. BMC Ophthalmology 23:1.
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Zhe Zhu & Jun Xiao. (2023) Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.“. BMC Ophthalmology 23:1.
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Robert M. Grainger, James D. Lauderdale, Janelle L. Collins, Kelly L. Trout, Shari McCullen Krantz, Susan S. Wolfe & Peter A. Netland. (2023) Report on the 2021 Aniridia North America symposium on PAX6, aniridia, and beyond. The Ocular Surface 29, pages 423-431.
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Kent W. Small. (2023) Letter to the Editor Regarding: "Modern diagnostic and therapeutic approaches in familial maculopathy with reference to North Carolina macular dystrophy" by Jana Nekolova et al.. Biomedical Papers 167:1, pages 95-97.
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Kent W. Small, Stijn Van de Sompele, Jessica Avetisjan, Nitin Udar, Steven Agemy, Elfride De Baere & Fadi S. Shaya. (2023) New Noncoding Base Pair Mutation at the Identical Locus as the Original NCMD/MCDR1 in a Mexican Family, Suggesting a Mutational Hotspot. Journal of VitreoRetinal Diseases 7:1, pages 33-42.
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Stijn Van de Sompele, Kent W. Small, Munevver Burcu Cicekdal, Víctor López Soriano, Eva D’haene, Fadi S. Shaya, Steven Agemy, Thijs Van der Snickt, Alfredo Dueñas Rey, Toon Rosseel, Mattias Van Heetvelde, Sarah Vergult, Irina Balikova, Arthur A. Bergen, Camiel J.F. Boon, Julie De Zaeytijd, Chris F. Inglehearn, Bohdan Kousal, Bart P. Leroy, Carlo Rivolta, Veronika Vaclavik, Jenneke van den Ende, Mary J. van Schooneveld, José Luis Gómez-Skarmeta, Juan J. Tena, Juan R. Martinez-Morales, Petra Liskova, Kris Vleminckx & Elfride De Baere. (2022) Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy. The American Journal of Human Genetics 109:11, pages 2029-2048.
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Johannes Birtel, Martin Gliem, Philipp Herrmann, Christine Neuhaus, Frank G Holz, Robert E MacLaren, Hendrik P N Scholl & Peter Charbel Issa. (2022) North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progression. British Journal of Ophthalmology 106:9, pages 1269-1273.
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Kent W. Small, Robert Wiggins, Nitin Udar, Rosemary Silva-Garcia, Jessica Avetisjan, Andrea Vincent & Fadi S. Shaya. (2022) North Carolina Macular Dystrophy: Long-term Follow-up of the Original Family. Ophthalmology Retina 6:6, pages 512-519.
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Isabelle Audo, Isabelle Meunier & José-Alain Sahel. 2022. Albert and Jakobiec's Principles and Practice of Ophthalmology. Albert and Jakobiec's Principles and Practice of Ophthalmology
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Kent W. Small, Elaine M. Tran, Leslie Small, Rajesh C. Rao & Fadi Shaya. (2019) Multimodal Imaging and Functional Testing in a North Carolina Macular Disease Family: Toxoplasmosis, Fovea Plana, and Torpedo Maculopathy Are Phenocopies. Ophthalmology Retina 3:7, pages 607-614.
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Francesco Pichi, Emad B. Abboud, Nicola G. Ghazi & Arif O. Khan. (2018) Fundus autofluorescence imaging in hereditary retinal diseases. Acta Ophthalmologica 96:5, pages e549-e561.
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Francesco Pichi, Mariachiara Morara, Chiara Veronese, Paolo Nucci & Antonio P. Ciardella. (2013) Multimodal Imaging in Hereditary Retinal Diseases. Journal of Ophthalmology 2013, pages 1-11.
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Daniel F. Kiernan, Rohan J. Shah, Seenu M. Hariprasad, Michael A. Grassi, Kent W. Small, Joseph P. Kiernan & William F. Mieler. (2011) Thirty-Year Follow-up of an African American Family with Macular Dystrophy of the Retina, Locus 1 (North Carolina Macular Dystrophy). Ophthalmology 118:7, pages 1435-1443.
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Krishna K. Singh, Steven Ristau, William W. Dawson, Michael Krawczak & Jörg Schmidtke. (2005) Mapping of a macular drusen susceptibility locus in rhesus macaques to the homologue of human chromosome 6q14-15. Experimental Eye Research 81:4, pages 401-406.
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Maurice F. Rabb, Lynne Mullen, Svetlana Yelchits, Nitin Udar & Kent W. Small. (1998) A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus. American Journal of Ophthalmology 125:4, pages 502-508.
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Mari Ann Z. Keithahn, Morgan Huang, John L. Keltner, Kent W. Small & Lawrence S. Morse. (1996) The Variable Expressivity of a Family with Central Areolar Pigment Epithelial Dystrophy. Ophthalmology 103:3, pages 406-415.
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