465 related articles for article (PubMed ID: 27485810)
1. Bull's eye and pigment maculopathy are further retinal manifestations of an abnormal Bruch's membrane in Alport syndrome.
Savige J; Wang Y; Crawford A; Smith J; Symons A; Mack H; Nicholls K; Wilson D; Colville D
Ophthalmic Genet; 2017; 38(3):238-244. PubMed ID: 27485810
[TBL] [Abstract][Full Text] [Related]
2. Retinal basement membrane abnormalities and the retinopathy of Alport syndrome.
Savige J; Liu J; DeBuc DC; Handa JT; Hageman GS; Wang YY; Parkin JD; Vote B; Fassett R; Sarks S; Colville D
Invest Ophthalmol Vis Sci; 2010 Mar; 51(3):1621-7. PubMed ID: 19850830
[TBL] [Abstract][Full Text] [Related]
3. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
Chen Y; Colville D; Ierino F; Symons A; Savige J
Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
[TBL] [Abstract][Full Text] [Related]
4. Ocular features in Alport syndrome: pathogenesis and clinical significance.
Savige J; Sheth S; Leys A; Nicholson A; Mack HG; Colville D
Clin J Am Soc Nephrol; 2015 Apr; 10(4):703-9. PubMed ID: 25649157
[TBL] [Abstract][Full Text] [Related]
5. Bull'S eye maculopathy in a patient taking sertraline.
Mason JO; Patel SA
Retin Cases Brief Rep; 2015; 9(2):131-3. PubMed ID: 25401995
[TBL] [Abstract][Full Text] [Related]
6. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
Shaw EA; Colville D; Wang YY; Zhang KW; Dagher H; Fassett R; Guymer R; Savige J
Nephrol Dial Transplant; 2007 Jan; 22(1):104-8. PubMed ID: 17071739
[TBL] [Abstract][Full Text] [Related]
7.
Cho IH; Kim HD; Jung SJ; Park TK
Indian J Ophthalmol; 2017 Sep; 65(9):877-879. PubMed ID: 28905837
[TBL] [Abstract][Full Text] [Related]
8. [A new case of giant macular hole in a patient with Alport syndrome].
Mercé E; Korobelnik JF; Delyfer MN; Rougier MB
J Fr Ophtalmol; 2012 Oct; 35(8):573-9. PubMed ID: 22695059
[TBL] [Abstract][Full Text] [Related]
9. Retinal findings in patients with Alport Syndrome: expanding the clinical spectrum.
Fawzi AA; Lee NG; Eliott D; Song J; Stewart JM
Br J Ophthalmol; 2009 Dec; 93(12):1606-11. PubMed ID: 19635720
[TBL] [Abstract][Full Text] [Related]
10. BULL'S EYE MACULOPATHY WITH MUTATIONS IN RDS/PRPH2 AND ROM-1.
Essilfie JO; Sanfilippo CJ; Sarraf D
Retin Cases Brief Rep; 2018 Fall; 12 Suppl 1():S55-S58. PubMed ID: 29155698
[TBL] [Abstract][Full Text] [Related]
11. Retinal dystrophies with bull's-eye maculopathy along with negative ERGs.
Nasser F; Kurtenbach A; Kohl S; Obermaier C; Stingl K; Zrenner E
Doc Ophthalmol; 2019 Aug; 139(1):45-57. PubMed ID: 30945053
[TBL] [Abstract][Full Text] [Related]
12. The retinal "lozenge" or "dull macular reflex" in Alport syndrome may be associated with a severe retinopathy and early-onset renal failure.
Colville D; Wang YY; Tan R; Savige J
Br J Ophthalmol; 2009 Mar; 93(3):383-6. PubMed ID: 19019929
[TBL] [Abstract][Full Text] [Related]
13. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.
Seddon JM; Afshari MA; Sharma S; Bernstein PS; Chong S; Hutchinson A; Petrukhin K; Allikmets R
Ophthalmology; 2001 Nov; 108(11):2060-7. PubMed ID: 11713080
[TBL] [Abstract][Full Text] [Related]
14. Autologous transplantation of retinal pigment epithelium-Bruch's membrane complex for hemorrhagic age-related macular degeneration.
Ma Z; Han L; Wang C; Dou H; Hu Y; Feng X; Xu Y; Wang Z; Yin Z; Liu Y
Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2975-81. PubMed ID: 19117919
[TBL] [Abstract][Full Text] [Related]
15. Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye Maculopathy.
Collison FT; Xie YA; Gambin T; Jhangiani S; Muzny D; Gibbs R; Lupski JR; Fishman GA; Allikmets R
Ophthalmic Genet; 2015; 36(3):270-5. PubMed ID: 25687216
[TBL] [Abstract][Full Text] [Related]
16. Bilateral giant macular holes: A rare manifestation of Alport syndrome.
Raimundo M; Fonseca C; Silva R; Figueira J
Eur J Ophthalmol; 2019 Jan; 29(1):NP13-NP16. PubMed ID: 29873249
[TBL] [Abstract][Full Text] [Related]
17. G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy.
Cella W; Greenstein VC; Zernant-Rajang J; Smith TR; Barile G; Allikmets R; Tsang SH
Exp Eye Res; 2009 Jun; 89(1):16-24. PubMed ID: 19217903
[TBL] [Abstract][Full Text] [Related]
18. [Rare ocular manifestation with suspect alport syndrome].
Krejčířová I; Varadyová B; Doležel Z; Autrata R; Matúšová J; Gregorová E
Cesk Slov Oftalmol; 2014 Jun; 70(3):114-8. PubMed ID: 25032798
[TBL] [Abstract][Full Text] [Related]
19. Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19).
Mizobuchi K; Hayashi T; Ohira R; Nakano T
Doc Ophthalmol; 2023 Jun; 146(3):281-291. PubMed ID: 37162688
[TBL] [Abstract][Full Text] [Related]
20. Temporal macular thinning associated with X-linked Alport syndrome.
Ahmed F; Kamae KK; Jones DJ; Deangelis MM; Hageman GS; Gregory MC; Bernstein PS
JAMA Ophthalmol; 2013 Jun; 131(6):777-82. PubMed ID: 23572034
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
