46 related articles for article (PubMed ID: 15579992)
1. Morphology and functional characteristics in adult vitelliform macular dystrophy.
Renner AB; Tillack H; Kraus H; Kohl S; Wissinger B; Mohr N; Weber BH; Kellner U; Foerster MH
Retina; 2004 Dec; 24(6):929-39. PubMed ID: 15579992
[TBL] [Abstract][Full Text] [Related]
2. Three-dimensional distribution of the vitelliform lesion, photoreceptors, and retinal pigment epithelium in the macula of patients with best vitelliform macular dystrophy.
Kay CN; Abramoff MD; Mullins RF; Kinnick TR; Lee K; Eyestone ME; Chung MM; Sohn EH; Stone EM
Arch Ophthalmol; 2012 Mar; 130(3):357-64. PubMed ID: 22084158
[TBL] [Abstract][Full Text] [Related]
3. Pseudovitelliform maculopathy associated with hereditary hemochromatosis.
Vukojevic A; Vukojevic M; Jukic T; Petricek I; Mandic K; Vukojevic N
Med Hypothesis Discov Innov Ophthalmol; 2023; 12(4):203-212. PubMed ID: 38601051
[TBL] [Abstract][Full Text] [Related]
4. Standardization of uveitis nomenclature for reporting clinical data. Results of the First International Workshop.
Jabs DA; Nussenblatt RB; Rosenbaum JT;
Am J Ophthalmol; 2005 Sep; 140(3):509-16. PubMed ID: 16196117
[TBL] [Abstract][Full Text] [Related]
5. Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene.
Querques G; Zerbib J; Santacroce R; Margaglione M; Delphin N; Rozet JM; Kaplan J; Martinelli D; Delle Noci N; Soubrane G; Souied EH
Mol Vis; 2009 Dec; 15():2960-72. PubMed ID: 20057903
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations.
Williams BN; Draper A; Lang PF; Lewis TR; Smith AL; Mayerl SJ; Rougié M; Simon JM; Arshavsky VY; Greenwald SH; Gamm DM; Pinilla I; Philpot BD
Hum Mol Genet; 2024 Feb; 33(5):448-464. PubMed ID: 37975905
[TBL] [Abstract][Full Text] [Related]
7. Electrophysiological Evaluation of Macular Dystrophies.
Chiang TK; Yu M
J Clin Med; 2023 Feb; 12(4):. PubMed ID: 36835965
[TBL] [Abstract][Full Text] [Related]
8. Deep learning to distinguish Best vitelliform macular dystrophy (BVMD) from adult-onset vitelliform macular degeneration (AVMD).
Crincoli E; Zhao Z; Querques G; Sacconi R; Carlà MM; Giannuzzi F; Ferrara S; Ribarich N; L'Abbate G; Rizzo S; Souied EH; Miere A
Sci Rep; 2022 Jul; 12(1):12745. PubMed ID: 35882966
[TBL] [Abstract][Full Text] [Related]
9. Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation.
Navinés-Ferrer A; Ruiz-Nogales S; Navarro R; Pomares E
Int J Mol Sci; 2022 Jul; 23(13):. PubMed ID: 35806438
[TBL] [Abstract][Full Text] [Related]
10. PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease.
Peeters MHCA; Khan M; Rooijakkers AAMB; Mulders T; Haer-Wigman L; Boon CJF; Klaver CCW; van den Born LI; Hoyng CB; Cremers FPM; den Hollander AI; Dhaenens CM; Collin RWJ
Hum Mutat; 2021 Dec; 42(12):1521-1547. PubMed ID: 34411390
[TBL] [Abstract][Full Text] [Related]
11. Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy.
Pfister TA; Zein WM; Cukras CA; Sen HN; Maldonado RS; Huryn LA; Hufnagel RB
Invest Ophthalmol Vis Sci; 2021 May; 62(6):22. PubMed ID: 34015078
[TBL] [Abstract][Full Text] [Related]
12. Bestrophinopathies: perspectives on clinical disease, Bestrophin-1 function and developing therapies.
Singh Grewal S; Smith JJ; Carr AF
Ther Adv Ophthalmol; 2021; 13():2515841421997191. PubMed ID: 33738427
[TBL] [Abstract][Full Text] [Related]
13. Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the
Hufendiek K; Hufendiek K; Jägle H; Stöhr H; Book M; Spital G; Rustambayova G; Framme C; Weber BHF; Renner AB; Kellner U
Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33302512
[TBL] [Abstract][Full Text] [Related]
14. Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy.
Ben Ner D; Sher I; Hamburg A; Mhajna MO; Chibel R; Derazne E; Sharvit-Ginon I; Pras E; Newman H; Levy J; Khateb S; Sharon D; Rotenstreich Y
Clin Ophthalmol; 2019; 13():465-475. PubMed ID: 30880907
[TBL] [Abstract][Full Text] [Related]
15. Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy.
Jun I; Lee JS; Lee JH; Lee CS; Choi SI; Gee HY; Lee MG; Kim EK
Sci Rep; 2017 Aug; 7(1):9146. PubMed ID: 28831140
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions.
Brandl C; Schulz HL; Charbel Issa P; Birtel J; Bergholz R; Lange C; Dahlke C; Zobor D; Weber BHF; Stöhr H
Genes (Basel); 2017 Jun; 8(7):. PubMed ID: 28644393
[TBL] [Abstract][Full Text] [Related]
17. Microperimetric evaluation in patients with adult-onset foveomacular vitelliform dystrophy.
Grenga PL; Fragiotta S; Cutini A; Meduri A; Vingolo EM
Indian J Ophthalmol; 2017 May; 65(5):385-389. PubMed ID: 28573994
[TBL] [Abstract][Full Text] [Related]
18. Clinical applications of fundus autofluorescence in retinal disease.
Yung M; Klufas MA; Sarraf D
Int J Retina Vitreous; 2016; 2():12. PubMed ID: 27847630
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of reticular pseudodrusen in newly presenting adult onset foveomacular vitelliform dystrophy.
Wilde C; Lakshmanan A; Patel M; Morales MU; Dhar-Munshi S; Amoaku WM
Eye (Lond); 2016 Jun; 30(6):817-24. PubMed ID: 27034200
[TBL] [Abstract][Full Text] [Related]
20. Ten-year follow-up of two unrelated patients with Müller cell sheen dystrophy and first report of successful vitrectomy.
Renner AB; Radeck V; Kellner U; Jägle H; Helbig H
Doc Ophthalmol; 2014 Dec; 129(3):191-202. PubMed ID: 25300407
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
