Simunovic MP - Search Results

1

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

2

The cone dystrophies.

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.

3

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.

4

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

5

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

6

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.

7

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

8

Visual Acuity after Retinal Gene Therapy for Choroideremia.

Edwards TL, Jolly JK, Groppe M, Barnard AR, Cottriall CL, Tolmachova T, Black GC, Webster AR, Lotery AJ, Holder GE, Xue K, Downes SM, Simunovic MP, Seabra MC, MacLaren RE. Edwards TL, et al. Among authors: simunovic mp. N Engl J Med. 2016 May 19;374(20):1996-8. doi: 10.1056/NEJMc1509501. Epub 2016 Apr 27. N Engl J Med. 2016. PMID: 27120491 Free PMC article. No abstract available.

9

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.

10

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

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