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Items: 10

Select item 10175411.

Annular choroidal sclerosis.

A. Chopdar

Br J Ophthalmol. 1976 Jul; 60(7): 512–516. doi: 10.1136/bjo.60.7.512

PMCID:: PMC1017541

Summary Page Browse PDF–2.2M

Select item 17360862.

Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy

J Lin, K Nishiguchi, M Nakamura, T Dryja, E Berson, Y Miyake

J Med Genet. 2005 Jun; 42(6): e38. doi: 10.1136/jmg.2004.029066

PMCID:: PMC1736086

Summary PDF–203K

Select item 60157293.

Phenotypic Expansion and Progression of SPATA7-associated Retinitis Pigmentosa

Jesse D. Sengillo, Winston Lee, Colleen G. Bilancia, Vaidehi Jobanputra, Stephen H. Tsang

Doc Ophthalmol. Author manuscript; available in PMC 2019 Apr 1.

Published in final edited form as: Doc Ophthalmol. 2018 Apr; 136(2): 125–133. Published online 2018 Feb 6. doi: 10.1007/s10633-018-9626-1

PMCID:: PMC6015729

Abstract Article PDF–818K

Select item 46623674.

Geographic atrophy in patients with advanced dry age-related macular degeneration: current challenges and future prospects

Ronald P Danis, Jeremy A Lavine, Amitha Domalpally

Clin Ophthalmol. 2015; 9: 2159–2174. Published online 2015 Nov 20. doi: 10.2147/OPTH.S92359

PMCID:: PMC4662367

Abstract Article PDF–2.0M

Select item 42997125.

Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy

Galuh D N Astuti, Vincent Sun, Miriam Bauwens, Ditta Zobor, Bart P Leroy, Amer Omar, Bernhard Jurklies, Irma Lopez, Huanan Ren, Volkan Yazar, Christian Hamel, Ulrich Kellner, Bernd Wissinger, Susanne Kohl, Elfride De Baere, Rob W J Collin, Robert K Koenekoop

Mol Genet Genomic Med. 2015 Jan; 3(1): 14–29. Published online 2014 Sep 15. doi: 10.1002/mgg3.109

PMCID:: PMC4299712

Abstract Article PDF–639K

Select item 28913596.

Fundus Autofluorescence, Optical Coherence Tomography, and Electroretinogram Findings in Choroidal Sclerosis

John C. Hwang, David Y. Kim, Chai Lin Chou, Stephen H. Tsang

Retina. Author manuscript; available in PMC 2011 Jul 1.

Published in final edited form as: Retina. 2010 Jul–Aug; 30(7): 1095–1103. doi: 10.1097/IAE.0b013e3181cd48f9

PMCID:: PMC2891359

Abstract Article PDF–9.1M

Select item 109660047.

Longitudinal structure-function analysis of molecularly-confirmed CYP4V2 Bietti Crystalline Dystrophy

Riccardo Cheloni, Neil Clough, Daniel Jackson, Mariya Moosajee

Eye (Lond) 2024 Apr; 38(5): 853–862. Published online 2023 Oct 28. doi: 10.1038/s41433-023-02791-7

PMCID:: PMC10966004

Abstract Article PDF–7.5M

Select item 102930348.

Full-field scotopic threshold improvement following voretigene neparvovec-rzyl treatment correlates with chorioretinal atrophy

Katarina Stingl, Krunoslav Stingl, Hillary Schwartz, Mark W. Reid, Melanie Kempf, Spyridon Dimopoulos, Friederike Kortuem, Mark S. Borchert, Thomas C. Lee, Aaron Nagiel

Ophthalmology. Author manuscript; available in PMC 2024 Jul 1.

Published in final edited form as: Ophthalmology. 2023 Jul; 130(7): 764–770. Published online 2023 Feb 21. doi: 10.1016/j.ophtha.2023.02.015

PMCID:: PMC10293034

Abstract Article PDF–1.3M

Select item 96515999.

Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence

Masha Kolesnikova, Jose Ronaldo Lima de Carvalho, Jr., Rait Parmann, Angela H. Kim, Vinit B. Mahajan, Stephen H. Tsang, Janet R. Sparrow

Mol Genet Genomic Med. 2022 Nov; 10(11): e2038. Published online 2022 Oct 12. doi: 10.1002/mgg3.2038

PMCID:: PMC9651599

Abstract Article PDF–1.4M

Select item 687007910.

Neural correlates of visual search in patients with hereditary retinal dystrophies

Tina Plank, Jozef Frolo, Fatima Farzana, Sabine Brandl‐Rühle, Agnes B. Renner, Mark W. Greenlee

Hum Brain Mapp. 2013 Oct; 34(10): 2607–2623. Published online 2012 Apr 16. doi: 10.1002/hbm.22088

PMCID:: PMC6870079

Abstract Article PDF–1.1M

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