Chelva E - Search Results

1

Acute progressive paravascular placoid neuroretinopathy with negative-type electroretinography in paraneoplastic retinopathy.

Chen FK, Chew AL, Zhang D, Chen SC, Chelva E, Chandrasekera E, Koay EMH, Forrester J, McLenachan S. Chen FK, et al. Among authors: chelva e. Doc Ophthalmol. 2017 Jun;134(3):227-235. doi: 10.1007/s10633-017-9587-9. Epub 2017 Apr 5. Doc Ophthalmol. 2017. PMID: 28382556 Free PMC article.

2

Thirteen-year follow up of isolated foveal retinoschisis in a 24-year-old woman.

Chen FK, McAllister IL, Chelva ES. Chen FK, et al. Clin Exp Ophthalmol. 2006 Aug;34(6):600-5. doi: 10.1111/j.1442-9071.2006.01283.x. Clin Exp Ophthalmol. 2006. PMID: 16925710

3

Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.

Crowley C, Paterson R, Lamey T, McLaren T, De Roach J, Chelva E, Khan J. Crowley C, et al. Among authors: chelva e. Doc Ophthalmol. 2014 Aug;129(1):57-63. doi: 10.1007/s10633-014-9444-z. Epub 2014 May 24. Doc Ophthalmol. 2014. PMID: 24859690 Free PMC article.

4

The effect of cobalt on the human eye.

Lim CA, Khan J, Chelva E, Khan R, Unsworth-Smith T. Lim CA, et al. Among authors: chelva e. Doc Ophthalmol. 2015 Feb;130(1):43-8. doi: 10.1007/s10633-014-9469-3. Epub 2014 Nov 8. Doc Ophthalmol. 2015. PMID: 25380579 Review.

5

FUNDUS AUTOFLUORESCENCE IN RUBELLA RETINOPATHY: Correlation With Photoreceptor Structure and Function.

Bukowska DM, Wan SL, Chew AL, Chelva E, Tang I, Mackey DA, Chen FK. Bukowska DM, et al. Among authors: chelva e. Retina. 2017 Jan;37(1):124-134. doi: 10.1097/IAE.0000000000001130. Retina. 2017. PMID: 28005720 Free article.

6

Perifoveal interdigitation zone loss in hydroxychloroquine toxicity leads to subclinical bull's eye lesion appearance on near-infrared reflectance imaging.

Chew AL, Sampson DM, Chelva E, Khan JC, Chen FK. Chew AL, et al. Among authors: chelva e. Doc Ophthalmol. 2018 Feb;136(1):57-68. doi: 10.1007/s10633-017-9615-9. Epub 2017 Nov 9. Doc Ophthalmol. 2018. PMID: 29124422 Free PMC article.

7

Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3).

Chen FK, Zhang X, Eintracht J, Zhang D, Arunachalam S, Thompson JA, Chelva E, Mallon D, Chen SC, McLaren T, Lamey T, De Roach J, McLenachan S. Chen FK, et al. Among authors: chelva e. Doc Ophthalmol. 2019 Feb;138(1):55-70. doi: 10.1007/s10633-018-9665-7. Epub 2018 Nov 16. Doc Ophthalmol. 2019. PMID: 30446867

8

ISCEV extended protocol for the S-cone ERG.

Perlman I, Kondo M, Chelva E, Robson AG, Holder GE. Perlman I, et al. Among authors: chelva e. Doc Ophthalmol. 2020 Apr;140(2):95-101. doi: 10.1007/s10633-019-09730-6. Epub 2019 Nov 20. Doc Ophthalmol. 2020. PMID: 31749034

9

Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect.

Huang D, Thompson JA, Charng J, Chelva E, McLenachan S, Chen SC, Zhang D, McLaren TL, Lamey TM, Constable IJ, De Roach JN, Aung-Htut MT, Adams A, Fletcher S, Wilton SD, Chen FK. Huang D, et al. Among authors: chelva e. Mol Genet Genomic Med. 2020 Jul;8(7):e1259. doi: 10.1002/mgg3.1259. Epub 2020 Apr 23. Mol Genet Genomic Med. 2020. PMID: 32627976 Free PMC article.

10

Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy.

Roshandel D, Thompson JA, Charng J, Zhang D, Chelva E, Arunachalam S, Attia MS, Lamey TM, McLaren TL, De Roach JN, Mackey DA, Wilton SD, Fletcher S, McLenachan S, Chen FK. Roshandel D, et al. Among authors: chelva e. Ophthalmic Genet. 2021 Feb;42(1):1-14. doi: 10.1080/13816810.2020.1827442. Epub 2020 Sep 27. Ophthalmic Genet. 2021. PMID: 32985313

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