Simunovic MP - Search Results

1

Simunovic MP, Moore AT. Simunovic MP, et al. Eye (Lond). 1998;12 ( Pt 3b):553-65. doi: 10.1038/eye.1998.145. Eye (Lond). 1998. PMID: 9775217 Review.

2

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.

Gregory-Evans K, Kelsell RE, Gregory-Evans CY, Downes SM, Fitzke FW, Holder GE, Simunovic M, Mollon JD, Taylor R, Hunt DM, Bird AC, Moore AT. Gregory-Evans K, et al. Ophthalmology. 2000 Jan;107(1):55-61. doi: 10.1016/s0161-6420(99)00038-x. Ophthalmology. 2000. PMID: 10647719

3

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2).

Michaelides M, Aligianis IA, Holder GE, Simunovic M, Mollon JD, Maher ER, Hunt DM, Moore AT. Michaelides M, et al. Br J Ophthalmol. 2003 Nov;87(11):1317-20. doi: 10.1136/bjo.87.11.1317. Br J Ophthalmol. 2003. PMID: 14609822 Free PMC article.

4

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.

Michaelides M, Johnson S, Simunovic MP, Bradshaw K, Holder G, Mollon JD, Moore AT, Hunt DM. Michaelides M, et al. Among authors: simunovic mp. Eye (Lond). 2005 Jan;19(1):2-10. doi: 10.1038/sj.eye.6701391. Eye (Lond). 2005. PMID: 15094734

5

X-linked cone dysfunction syndrome with myopia and protanopia.

Michaelides M, Johnson S, Bradshaw K, Holder GE, Simunovic MP, Mollon JD, Moore AT, Hunt DM. Michaelides M, et al. Among authors: simunovic mp. Ophthalmology. 2005 Aug;112(8):1448-54. doi: 10.1016/j.ophtha.2005.02.021. Ophthalmology. 2005. PMID: 15953640

6

Selective Automated Perimetry Under Photopic, Mesopic, and Scotopic Conditions: Detection Mechanisms and Testing Strategies.

Simunovic MP, Moore AT, MacLaren RE. Simunovic MP, et al. Transl Vis Sci Technol. 2016 May 20;5(3):10. doi: 10.1167/tvst.5.3.10. eCollection 2016 May. Transl Vis Sci Technol. 2016. PMID: 27247858 Free PMC article.

7

THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT: A NEW TREATMENT OUTCOME AND NATURAL HISTORY REGISTRY FOR INHERITED RETINAL DISEASE.

Simunovic MP, Moore AT, Grigg J, Sergouniotis P, Mahroo OA, Vincent A, Singh M, Fischer MD, Edwards T, Mack H, Hogden M, Chen FK, Hewitt A, Ayton L, Leroy B, Jamieson R, Gillies MC, Barthelmes D. Simunovic MP, et al. Retina. 2024 Oct 10. doi: 10.1097/IAE.0000000000004296. Online ahead of print. Retina. 2024. PMID: 39418576

8

Colour discrimination ellipses in patients with dominant optic atrophy.

Simunovic MP, Votruba M, Regan BC, Mollon JD. Simunovic MP, et al. Vision Res. 1998 Nov;38(21):3413-9. doi: 10.1016/s0042-6989(98)00094-7. Vision Res. 1998. PMID: 9893858 Free article.

9

Is color vision deficiency an advantage under scotopic conditions?

Simunovic MP, Regan BC, Mollon JD. Simunovic MP, et al. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3357-64. Invest Ophthalmol Vis Sci. 2001. PMID: 11726645

10

How well does color perimetry isolate responses from individual cone mechanisms?

Simunovic MP, Cullerne A, Colley A, Wilson TD. Simunovic MP, et al. J Glaucoma. 2004 Feb;13(1):22-7. doi: 10.1097/00061198-200402000-00005. J Glaucoma. 2004. PMID: 14704539

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