140 related articles for article (PubMed ID: 27474146)
1. Martinique Crinkled Retinal Pigment Epitheliopathy: Clinical Stages and Pathophysiologic Insights.
Jean-Charles A; Merle H; Audo I; Desoudin C; Bocquet B; Baudoin C; Sidibe M; Mauget-Faÿsse M; Wolff B; Fichard A; Lenaers G; Sahel JA; Gaudric A; Cohen SY; Hamel CP; Meunier I
Ophthalmology; 2016 Oct; 123(10):2196-204. PubMed ID: 27474146
[TBL] [Abstract][Full Text] [Related]
2. A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium.
Meunier I; Lenaers G; Bocquet B; Baudoin C; Piro-Megy C; Cubizolle A; Quilès M; Jean-Charles A; Cohen SY; Merle H; Gaudric A; Labesse G; Manes G; Péquignot M; Cazevieille C; Dhaenens CM; Fichard A; Ronkina N; Arthur SJ; Gaestel M; Hamel CP
Hum Mol Genet; 2016 Mar; 25(5):916-26. PubMed ID: 26744326
[TBL] [Abstract][Full Text] [Related]
3. Martinique (West Indies) crinkled retinal pigment epitheliopathy: clinical description.
Jean-Charles A; Cohen SY; Merle H; Quentel G; Legargasson JF; Gaudric A
Retina; 2013 May; 33(5):1041-8. PubMed ID: 23370609
[TBL] [Abstract][Full Text] [Related]
4. [Martinique crinkled retinal pigment epitheliopathy (MCRPE): A case report].
Croisé F; Le Lez ML; Pisella PJ
J Fr Ophtalmol; 2019 May; 42(5):e225-e228. PubMed ID: 30955902
[No Abstract] [Full Text] [Related]
5. Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.
Qian CX; Charran D; Strong CR; Steffens TJ; Jayasundera T; Heckenlively JR
Ophthalmology; 2017 Apr; 124(4):456-463. PubMed ID: 28187978
[TBL] [Abstract][Full Text] [Related]
6. Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.
Hull S; Arno G; Robson AG; Broadgate S; Plagnol V; McKibbin M; Halford S; Michaelides M; Holder GE; Moore AT; Khan KN; Webster AR
JAMA Ophthalmol; 2016 Sep; 134(9):992-1000. PubMed ID: 27386845
[TBL] [Abstract][Full Text] [Related]
7. Pachychoroid pigment epitheliopathy.
Warrow DJ; Hoang QV; Freund KB
Retina; 2013 Sep; 33(8):1659-72. PubMed ID: 23751942
[TBL] [Abstract][Full Text] [Related]
8. Sorsby Fundus Dystrophy: Novel Mutations, Novel Phenotypic Characteristics, and Treatment Outcomes.
Gliem M; Müller PL; Mangold E; Holz FG; Bolz HJ; Stöhr H; Weber BH; Charbel Issa P
Invest Ophthalmol Vis Sci; 2015 Apr; 56(4):2664-76. PubMed ID: 25766588
[TBL] [Abstract][Full Text] [Related]
9. Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers.
Murro V; Mucciolo DP; Passerini I; Palchetti S; Sodi A; Virgili G; Rizzo S
Graefes Arch Clin Exp Ophthalmol; 2017 Nov; 255(11):2099-2111. PubMed ID: 28752371
[TBL] [Abstract][Full Text] [Related]
10. Improved visualization of polypoidal choroidal vasculopathy lesions using spectral-domain optical coherence tomography.
Ojima Y; Hangai M; Sakamoto A; Tsujikawa A; Otani A; Tamura H; Yoshimura N
Retina; 2009 Jan; 29(1):52-9. PubMed ID: 18827738
[TBL] [Abstract][Full Text] [Related]
11. Pachychoroid neovasculopathy: aspect on optical coherence tomography angiography.
Azar G; Wolff B; Mauget-Faÿsse M; Rispoli M; Savastano MC; Lumbroso B
Acta Ophthalmol; 2017 Jun; 95(4):421-427. PubMed ID: 27597633
[TBL] [Abstract][Full Text] [Related]
12. Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy.
Murro V; Mucciolo DP; Sodi A; Passerini I; Giorgio D; Virgili G; Rizzo S
Graefes Arch Clin Exp Ophthalmol; 2019 Jan; 257(1):9-22. PubMed ID: 30324420
[TBL] [Abstract][Full Text] [Related]
13. REGRESSION OF TYPE 2 NEOVASCULARIZATION INTO A TYPE 1 PATTERN AFTER INTRAVITREAL ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY FOR NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.
Dolz-Marco R; Phasukkijwatana N; Sarraf D; Freund KB
Retina; 2017 Feb; 37(2):222-233. PubMed ID: 27627752
[TBL] [Abstract][Full Text] [Related]
14. Spectral domain optical coherence tomography classification of acute posterior multifocal placoid pigment epitheliopathy.
Goldenberg D; Habot-Wilner Z; Loewenstein A; Goldstein M
Retina; 2012 Jul; 32(7):1403-10. PubMed ID: 22466468
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.
de Laat P; Smeitink JAM; Janssen MCH; Keunen JEE; Boon CJF
Ophthalmology; 2013 Dec; 120(12):2684-2696. PubMed ID: 23806424
[TBL] [Abstract][Full Text] [Related]
16. Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome.
Ozawa K; Mochizuki K; Manabe Y; Yoshikura N; Shimohata T; Nishino I; Goto YI
Doc Ophthalmol; 2019 Apr; 138(2):147-152. PubMed ID: 30701423
[TBL] [Abstract][Full Text] [Related]
17. Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.
Katagiri S; Hayashi T; Yoshitake K; Akahori M; Ikeo K; Gekka T; Tsuneoka H; Iwata T
Ophthalmic Genet; 2016; 37(1):68-75. PubMed ID: 25113443
[TBL] [Abstract][Full Text] [Related]
18. Atypical retinal pigment epithelial defects with retained photoreceptor layers: a so far disregarded finding in age related macular degeneration.
Giannakaki-Zimmermann H; Querques G; Munch IC; Shroff D; Sarraf D; Chen X; Cunha-Souza E; Mrejen S; Capuano V; Rodrigues MW; Gupta C; Ebneter A; Zinkernagel MS; Munk MR
BMC Ophthalmol; 2017 May; 17(1):67. PubMed ID: 28506260
[TBL] [Abstract][Full Text] [Related]
19. Simultaneous investigation of vascular and retinal pigment epithelial pathologies of exudative macular diseases by multifunctional optical coherence tomography.
Hong YJ; Miura M; Ju MJ; Makita S; Iwasaki T; Yasuno Y
Invest Ophthalmol Vis Sci; 2014 Jul; 55(8):5016-31. PubMed ID: 25052993
[TBL] [Abstract][Full Text] [Related]
20. Characteristic spectral-domain optical coherence tomography findings of multifocal choroiditis.
Vance SK; Khan S; Klancnik JM; Freund KB
Retina; 2011 Apr; 31(4):717-23. PubMed ID: 21386760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
