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Literature DB >> 15180246

Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.

Anthony G Robson¹, Catherine Egan, Graham E Holder, Alan C Bird, Fred W Fitzke.

Abstract

Entities: Disease

Mesh：

Year: 2003 PMID： 15180246 DOI： 10.1007/978-1-4615-0067-4_6

Source DB: PubMed Journal: Adv Exp Med Biol ISSN： 0065-2598 Impact factor: 2.622

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Cited

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12 in total

1. Autofluorescence and High-Resolution OCT Findings Revealed Ciliopathy in Senior-Loken Syndrome.

Authors: Wener Cella; Luiz H Lima; Nan-Kai Wang; Joaquin Tosi; Lawrence A Yannuzzi; Stephen H Tsang
Journal: Ophthalmic Surg Lasers Imaging Date: 2010-03-09

2. Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Authors: A G Robson; Z Saihan; S A Jenkins; F W Fitzke; A C Bird; A R Webster; G E Holder
Journal: Br J Ophthalmol Date: 2006-04 Impact factor: 4.638

3. Bilateral Concordance of the Fundus Hyperautofluorescent Ring in Typical Retinitis Pigmentosa Patients.

Authors: Tharikarn Sujirakul; Richard Davis; Deniz Erol; Lijuan Zhang; Giuseppe Schillizzi; Leticia Royo-Dujardin; Sherry Shen; Stephen Tsang
Journal: Ophthalmic Genet Date: 2013-10-10 Impact factor: 1.803

4. Correlation of ultra-widefield fundus autofluorescence patterns with the underlying genotype in retinal dystrophies and retinitis pigmentosa.

Authors: George Trichonas; Elias I Traboulsi; Justis P Ehlers
Journal: Ophthalmic Genet Date: 2016-11-23 Impact factor: 1.803

Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.

1. Autofluorescence and High-Resolution OCT Findings Revealed Ciliopathy in Senior-Loken Syndrome.

2. Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

3. Bilateral Concordance of the Fundus Hyperautofluorescent Ring in Typical Retinitis Pigmentosa Patients.

4. Correlation of ultra-widefield fundus autofluorescence patterns with the underlying genotype in retinal dystrophies and retinitis pigmentosa.

5. Progressive constriction of the hyperautofluorescent ring in retinitis pigmentosa.

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

7. Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N.

8. Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene.

9. Structural assessment of hyperautofluorescent ring in patients with retinitis pigmentosa.

10. Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.