223 related articles for article (PubMed ID: 32679203)
21. 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]
22. 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]
23. Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Khan KN; Kasilian M; Mahroo OAR; Tanna P; Kalitzeos A; Robson AG; Tsunoda K; Iwata T; Moore AT; Fujinami K; Michaelides M
Ophthalmology; 2018 May; 125(5):735-746. PubMed ID: 29310964
[TBL] [Abstract][Full Text] [Related]
24. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.
Orès R; Mohand-Said S; Dhaenens CM; Antonio A; Zeitz C; Augstburger E; Andrieu C; Sahel JA; Audo I
Ophthalmology; 2018 Oct; 125(10):1587-1596. PubMed ID: 29739629
[TBL] [Abstract][Full Text] [Related]
25. A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome.
Rocha-Sousa A; Hayashi T; Gomes NL; Penas S; Brandão E; Rocha P; Urashima M; Yamada H; Tsuneoka H; Falcão-Reis F
Graefes Arch Clin Exp Ophthalmol; 2011 Feb; 249(2):201-8. PubMed ID: 20725840
[TBL] [Abstract][Full Text] [Related]
26. Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults.
Park SP; Hong IH; Tsang SH; Lee W; Horowitz J; Yzer S; Allikmets R; Chang S
Graefes Arch Clin Exp Ophthalmol; 2013 Oct; 251(10):2299-309. PubMed ID: 23604511
[TBL] [Abstract][Full Text] [Related]
27. Hyperautofluorescent macular ring in a series of patients with enhanced S-cone syndrome.
Gelman R; Greenberg JP; Duncker T; Nguyen HV; Yannuzzi LA; Tsang SH
Ophthalmic Surg Lasers Imaging Retina; 2014; 45(6):592-5. PubMed ID: 25423642
[TBL] [Abstract][Full Text] [Related]
28. Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.
Talib M; van Schooneveld MJ; van Genderen MM; Wijnholds J; Florijn RJ; Ten Brink JB; Schalij-Delfos NE; Dagnelie G; Cremers FPM; Wolterbeek R; Fiocco M; Thiadens AA; Hoyng CB; Klaver CC; Bergen AA; Boon CJF
Ophthalmology; 2017 Jun; 124(6):884-895. PubMed ID: 28341475
[TBL] [Abstract][Full Text] [Related]
29. Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variant.
Cehajic-Kapetanovic J; Cottriall CL; Jolly JK; Shanks M; Clouston P; Charbel Issa P; MacLaren RE
Ophthalmic Genet; 2019 Feb; 40(1):29-33. PubMed ID: 30466340
[TBL] [Abstract][Full Text] [Related]
30. Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients.
Murakami Y; Koyanagi Y; Fukushima M; Yoshimura M; Fujiwara K; Akiyama M; Momozawa Y; Ueno S; Terasaki H; Oishi A; Miyata M; Ikeda H; Tsujikawa A; Mizobuchi K; Hayashi T; Fujinami K; Tsunoda K; Park JY; Han J; Kim M; Lee CS; Kim SJ; Park TK; Joo K; Woo SJ; Ikeda Y; Sonoda KH
Ophthalmol Retina; 2021 Dec; 5(12):1269-1279. PubMed ID: 33636399
[TBL] [Abstract][Full Text] [Related]
31. Characterization of Chorioretinopathy Associated with Mitochondrial Trifunctional Protein Disorders: Long-Term Follow-up of 21 Cases.
Boese EA; Jain N; Jia Y; Schlechter CL; Harding CO; Gao SS; Patel RC; Huang D; Weleber RG; Gillingham MB; Pennesi ME
Ophthalmology; 2016 Oct; 123(10):2183-95. PubMed ID: 27491397
[TBL] [Abstract][Full Text] [Related]
32. PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY: Detailed Clinical Study of a Large Cohort.
Shona OA; Islam F; Robson AG; Webster AR; Moore AT; Michaelides M
Retina; 2019 Mar; 39(3):514-529. PubMed ID: 29300249
[TBL] [Abstract][Full Text] [Related]
33. Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the
De Zaeytijd J; Coppieters F; De Bruyne M; Van Royen J; Roels D; Six R; Van Cauwenbergh C; De Baere E; Leroy BP
Ophthalmic Genet; 2021 Oct; 42(5):521-532. PubMed ID: 33949280
[No Abstract] [Full Text] [Related]
34. Enhanced S-cone syndrome with preserved macular structure and severely depressed retinal function.
Cima I; Brecelj J; Sustar M; Coppieters F; Leroy BP; De Baere E; Hawlina M
Doc Ophthalmol; 2012 Oct; 125(2):161-8. PubMed ID: 22711506
[TBL] [Abstract][Full Text] [Related]
35. Early-onset stargardt disease: phenotypic and genotypic characteristics.
Lambertus S; van Huet RA; Bax NM; Hoefsloot LH; Cremers FP; Boon CJ; Klevering BJ; Hoyng CB
Ophthalmology; 2015 Feb; 122(2):335-44. PubMed ID: 25444351
[TBL] [Abstract][Full Text] [Related]
36. Highly Variable Disease Courses in Siblings with Stargardt Disease.
Valkenburg D; Runhart EH; Bax NM; Liefers B; Lambertus SL; Sánchez CI; Cremers FPM; Hoyng CB
Ophthalmology; 2019 Dec; 126(12):1712-1721. PubMed ID: 31522899
[TBL] [Abstract][Full Text] [Related]
37. KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1.
Georgiou M; Robson AG; Fujinami K; Leo SM; Vincent A; Nasser F; Cabral De Guimarães TA; Khateb S; Pontikos N; Fujinami-Yokokawa Y; Liu X; Tsunoda K; Hayashi T; Vargas ME; Thiadens AAHJ; de Carvalho ER; Nguyen XT; Arno G; Mahroo OA; Martin-Merida MI; Jimenez-Rolando B; Gordo G; Carreño E; Ayuso C; Sharon D; Kohl S; Huckfeldt RM; Wissinger B; Boon CJF; Banin E; Pennesi ME; Khan AO; Webster AR; Zrenner E; Héon E; Michaelides M
Am J Ophthalmol; 2021 May; 225():95-107. PubMed ID: 33309813
[TBL] [Abstract][Full Text] [Related]
38. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
[TBL] [Abstract][Full Text] [Related]
39. Cystoid macular lesions are resistant to topical dorzolamide treatment in enhanced S-cone syndrome child.
Bušić M; Bjeloš M; Bosnar D; Ramić S; Bušić I
Doc Ophthalmol; 2016 Feb; 132(1):67-73. PubMed ID: 26803827
[TBL] [Abstract][Full Text] [Related]
40. Multimodal imaging of foveal cavitation in retinal dystrophies.
Parodi MB; Cicinelli MV; Iacono P; Bolognesi G; Bandello F
Graefes Arch Clin Exp Ophthalmol; 2017 Feb; 255(2):271-279. PubMed ID: 27491512
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
