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Results: 1 to 20 of 101

1.

Fine central macular dots associated with childhood-onset Stargardt Disease.

Fujinami K, Singh R, Carroll J, Zernant J, Allikmets R, Michaelides M, Moore AT.

Acta Ophthalmol. 2014 Mar;92(2):e157-9. doi: 10.1111/aos.12259. Epub 2013 Sep 11. No abstract available.

PMID:
24020726
[PubMed - indexed for MEDLINE]
2.

Stargardt disease with preserved central vision: identification of a putative novel mutation in ATP-binding cassette transporter gene.

Fujinami K, Akahori M, Fukui M, Tsunoda K, Iwata T, Miyake Y.

Acta Ophthalmol. 2011 May;89(3):e297-8. doi: 10.1111/j.1755-3768.2009.01848.x. No abstract available.

PMID:
20163366
[PubMed - indexed for MEDLINE]
3.

Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.

Burke TR, Fishman GA, Zernant J, Schubert C, Tsang SH, Smith RT, Ayyagari R, Koenekoop RK, Umfress A, Ciccarelli ML, Baldi A, Iannaccone A, Cremers FP, Klaver CC, Allikmets R.

Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4458-67. doi: 10.1167/iovs.11-9166.

PMID:
22661473
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Stargardt disease in a patient with retinoblastoma.

Margalit E, Sunness JS, Green WR, Kelman SE, Schachat AP, Fiergang D, Allikmets R.

Arch Ophthalmol. 2003 Nov;121(11):1643-6. No abstract available.

PMID:
14609928
[PubMed - indexed for MEDLINE]
5.

Disruption in Bruch membrane in patients with Stargardt disease.

Park SP, Chang S, Allikmets R, Smith RT, Burke TR, Gregory-Roberts E, Tsang SH.

Ophthalmic Genet. 2012 Mar;33(1):49-52. doi: 10.3109/13816810.2011.628358. Epub 2011 Nov 7.

PMID:
22060670
[PubMed - indexed for MEDLINE]
6.

Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.

Chen Y, Ratnam K, Sundquist SM, Lujan B, Ayyagari R, Gudiseva VH, Roorda A, Duncan JL.

Invest Ophthalmol Vis Sci. 2011 May 17;52(6):3281-92. doi: 10.1167/iovs.10-6538.

PMID:
21296825
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.

Testa F, Rossi S, Sodi A, Passerini I, Di Iorio V, Della Corte M, Banfi S, Surace EM, Menchini U, Auricchio A, Simonelli F.

Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4409-15. doi: 10.1167/iovs.11-8201.

PMID:
22661472
[PubMed - indexed for MEDLINE]
Free Article
8.

A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.

Zhang K, Garibaldi DC, Kniazeva M, Albini T, Chiang MF, Kerrigan M, Sunness JS, Han M, Allikmets R.

Am J Ophthalmol. 1999 Dec;128(6):720-4.

PMID:
10612508
[PubMed - indexed for MEDLINE]
9.

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.

Fujinami K, Sergouniotis PI, Davidson AE, Wright G, Chana RK, Tsunoda K, Tsubota K, Egan CA, Robson AG, Moore AT, Holder GE, Michaelides M, Webster AR.

Am J Ophthalmol. 2013 Sep;156(3):487-501.e1. doi: 10.1016/j.ajo.2013.05.003.

PMID:
23953153
[PubMed - indexed for MEDLINE]
10.

Phenotypic heterogeneity and lesion size measurements in Stargardt macular dystrophy.

Shah SN, Koozekanani DD, Kim JE.

Ophthalmic Surg Lasers Imaging. 2009 Sep-Oct;40(5):506-12. doi: 10.3928/15428877-20090901-14.

PMID:
19772279
[PubMed - indexed for MEDLINE]
11.

Peripapillary dark choroid ring as a helpful diagnostic sign in advanced stargardt disease.

Jayasundera T, Rhoades W, Branham K, Niziol LM, Musch DC, Heckenlively JR.

Am J Ophthalmol. 2010 Apr;149(4):656-660.e2. doi: 10.1016/j.ajo.2009.11.005. Epub 2010 Feb 6.

PMID:
20138608
[PubMed - indexed for MEDLINE]
12.

Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging.

Ritter M, Zotter S, Schmidt WM, Bittner RE, Deak GG, Pircher M, Sacu S, Hitzenberger CK, Schmidt-Erfurth UM; Macula Study Group Vienna.

Invest Ophthalmol Vis Sci. 2013 Sep 27;54(9):6416-25. doi: 10.1167/iovs.12-11550.

PMID:
23882696
[PubMed - indexed for MEDLINE]
13.

Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.

Bini A, Sodi A, Passerini I, Menchini U, Torricelli F.

Clin Experiment Ophthalmol. 2007 Nov;35(8):777-9.

PMID:
17997789
[PubMed - indexed for MEDLINE]
14.

Abnormality in the external limiting membrane in early Stargardt disease.

Burke TR, Yzer S, Zernant J, Smith RT, Tsang SH, Allikmets R.

Ophthalmic Genet. 2013 Mar-Jun;34(1-2):75-7. doi: 10.3109/13816810.2012.707271. Epub 2012 Aug 7.

PMID:
22871184
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease.

Miraldi Utz V, Coussa RG, Marino MJ, Chappelow AV, Pauer GJ, Hagstrom SA, Traboulsi EI.

Br J Ophthalmol. 2014 Apr;98(4):513-8. doi: 10.1136/bjophthalmol-2013-304270. Epub 2014 Jan 23.

PMID:
24457364
[PubMed - indexed for MEDLINE]
16.

The clinical effect of homozygous ABCA4 alleles in 18 patients.

Fujinami K, Sergouniotis PI, Davidson AE, Mackay DS, Tsunoda K, Tsubota K, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR.

Ophthalmology. 2013 Nov;120(11):2324-31. doi: 10.1016/j.ophtha.2013.04.016. Epub 2013 Jun 12.

PMID:
23769331
[PubMed - indexed for MEDLINE]
17.

Occurrence of full-thickness macular hole complicating Stargardt disease with ABCR mutation.

Sodi A, Bini A, Passerini I, Menchini U, Torricelli F.

Eur J Ophthalmol. 2006 Mar-Apr;16(2):335-8.

PMID:
16703556
[PubMed - indexed for MEDLINE]
18.

Quantification of peripapillary sparing and macular involvement in Stargardt disease (STGD1).

Burke TR, Rhee DW, Smith RT, Tsang SH, Allikmets R, Chang S, Lazow MA, Hood DC, Greenstein VC.

Invest Ophthalmol Vis Sci. 2011 Oct 10;52(11):8006-15. doi: 10.1167/iovs.11-7693.

PMID:
21873672
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

The dark atrophy with indocyanine green angiography in Stargardt disease.

Giani A, Pellegrini M, Carini E, Peroglio Deiro A, Bottoni F, Staurenghi G.

Invest Ophthalmol Vis Sci. 2012 Jun 26;53(7):3999-4004. doi: 10.1167/iovs.11-9258.

PMID:
22589445
[PubMed - indexed for MEDLINE]
Free Article
20.

Allelic and phenotypic heterogeneity in ABCA4 mutations.

Burke TR, Tsang SH.

Ophthalmic Genet. 2011 Sep;32(3):165-74. doi: 10.3109/13816810.2011.565397. Epub 2011 Apr 21. Review.

PMID:
21510770
[PubMed - indexed for MEDLINE]
Free PMC Article

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