218 related articles for article (PubMed ID: 32679203)
1. Enhanced S-Cone Syndrome: Spectrum of Clinical, Imaging, Electrophysiologic, and Genetic Findings in a Retrospective Case Series of 56 Patients.
de Carvalho ER; Robson AG; Arno G; Boon CJF; Webster AA; Michaelides M
Ophthalmol Retina; 2021 Feb; 5(2):195-214. PubMed ID: 32679203
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular characterization of enhanced S-cone syndrome in children.
Hull S; Arno G; Sergouniotis PI; Tiffin P; Borman AD; Chandra A; Robson AG; Holder GE; Webster AR; Moore AT
JAMA Ophthalmol; 2014 Nov; 132(11):1341-9. PubMed ID: 25079116
[TBL] [Abstract][Full Text] [Related]
3. Enhanced S-cone syndrome: Clinical spectrum in Indian population.
Naik A; Ratra D; Banerjee A; Dalan D; Jandyal S; Rao G; Sen P; Bhende M; Jayaprakash V; Susvar P; Walinjkar J; Rao C
Indian J Ophthalmol; 2019 Apr; 67(4):523-529. PubMed ID: 30900587
[TBL] [Abstract][Full Text] [Related]
4. Recognizable Patterns of Submacular Fibrosis in Enhanced S-Cone Syndrome.
Alsalamah AK; Khan AO; Bakar AA; Schatz P; Nowilaty SR
Ophthalmol Retina; 2021 Sep; 5(9):918-927. PubMed ID: 33819700
[TBL] [Abstract][Full Text] [Related]
5. Expanded clinical spectrum of enhanced S-cone syndrome.
Yzer S; Barbazetto I; Allikmets R; van Schooneveld MJ; Bergen A; Tsang SH; Jacobson SG; Yannuzzi LA
JAMA Ophthalmol; 2013 Oct; 131(10):1324-30. PubMed ID: 23989059
[TBL] [Abstract][Full Text] [Related]
6. Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report.
Minnella AM; Pagliei V; Savastano MC; Federici M; Bertelli M; Maltese PE; Placidi G; Corbo G; Falsini B; Caporossi A
J Med Case Rep; 2018 Oct; 12(1):287. PubMed ID: 30285900
[TBL] [Abstract][Full Text] [Related]
7. New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.
Kuniyoshi K; Hayashi T; Sakuramoto H; Mishima H; Tsuneoka H; Tsunoda K; Iwata T; Shimomura Y
Jpn J Ophthalmol; 2016 Nov; 60(6):476-485. PubMed ID: 27522502
[TBL] [Abstract][Full Text] [Related]
8. Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone Syndrome.
Newman H; Blumen SC; Braverman I; Hanna R; Tiosano B; Perlman I; Ben-Yosef T
Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5361-5371. PubMed ID: 27732723
[TBL] [Abstract][Full Text] [Related]
9. RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History.
Georgiou M; Robson AG; Jovanovic K; Guimarães TAC; Ali N; Pontikos N; Uwaydat SH; Mahroo OA; Cheetham ME; Webster AR; Hardcastle AJ; Michaelides M
Ophthalmology; 2023 Apr; 130(4):413-422. PubMed ID: 36423731
[TBL] [Abstract][Full Text] [Related]
10. An Examination of the Propositus of Enhanced S-Cone Syndrome 30 Years After Diagnosis.
Marmor MF
JAMA Ophthalmol; 2020 Sep; 138(9):1004-1006. PubMed ID: 32722798
[No Abstract] [Full Text] [Related]
11. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
Nishiguchi KM; Ikeda Y; Fujita K; Kunikata H; Akiho M; Hashimoto K; Hosono K; Kurata K; Koyanagi Y; Akiyama M; Suzuki T; Kawasaki R; Wada Y; Hotta Y; Sonoda KH; Murakami A; Nakazawa M; Nakazawa T; Abe T
Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
[TBL] [Abstract][Full Text] [Related]
12. RETINOCHOROIDAL ANASTOMOSIS ASSOCIATED WITH ENHANCED S-CONE SYNDROME.
Zerbib J; Blanco Garavito R; Gerber S; Oubraham H; Sikorav A; Audo I; Kaplan J; Rozet JM; Souied EH
Retin Cases Brief Rep; 2019; 13(4):295-299. PubMed ID: 28541266
[TBL] [Abstract][Full Text] [Related]
13. Incidence and Natural History of Retinochoroidal Neovascularization in Enhanced S-Cone Syndrome.
Nowilaty SR; Alsalamah AK; Magliyah MS; Alabdullah AA; Ahmad K; Semidey VA; Mura M; Schatz P
Am J Ophthalmol; 2021 Feb; 222():174-184. PubMed ID: 32941856
[TBL] [Abstract][Full Text] [Related]
14. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
Sustar M; Perovšek D; Cima I; Stirn-Kranjc B; Hawlina M; Brecelj J
Doc Ophthalmol; 2015 Jun; 130(3):165-77. PubMed ID: 25663266
[TBL] [Abstract][Full Text] [Related]
15. Benign Yellow Dot Maculopathy: A New Macular Phenotype.
Dev Borman A; Rachitskaya A; Suzani M; Sisk RA; Ahmed ZM; Holder GE; Cipriani V; Arno G; Webster AR; Hufnagel RB; Berrocal A; Moore AT
Ophthalmology; 2017 Jul; 124(7):1004-1013. PubMed ID: 28366503
[TBL] [Abstract][Full Text] [Related]
16. Novel findings in enhanced S-cone syndrome: a case with macular retinal neovascularization and severe retinal vasculitis.
Bazvand F; Khojasteh H; Zarei M
Doc Ophthalmol; 2019 Dec; 139(3):221-226. PubMed ID: 31292819
[TBL] [Abstract][Full Text] [Related]
17. Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical Trials.
Casalino G; Khan KN; Armengol M; Wright G; Pontikos N; Georgiou M; Webster AR; Robson AG; Grewal PS; Michaelides M
Ophthalmology; 2021 May; 128(5):706-718. PubMed ID: 33039401
[TBL] [Abstract][Full Text] [Related]
18. Clinical and molecular characteristics of childhood-onset Stargardt disease.
Fujinami K; Zernant J; Chana RK; Wright GA; Tsunoda K; Ozawa Y; Tsubota K; Robson AG; Holder GE; Allikmets R; Michaelides M; Moore AT
Ophthalmology; 2015 Feb; 122(2):326-34. PubMed ID: 25312043
[TBL] [Abstract][Full Text] [Related]
19. Pigmented Paravenous Chorioretinal Atrophy: Clinical Spectrum and Multimodal Imaging Characteristics.
Lee EK; Lee SY; Oh BL; Yoon CK; Park UC; Yu HG
Am J Ophthalmol; 2021 Apr; 224():120-132. PubMed ID: 33340506
[TBL] [Abstract][Full Text] [Related]
20. A DOUBLE HYPERAUTOFLUORESCENT RING IN A 33-YEAR-OLD-FEMALE PATIENT.
da Palma MM; Marra M; Pennesi ME
Retin Cases Brief Rep; 2023 Jun; 17(4S):S15-S18. PubMed ID: 36067420
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
