Search Results - "Cohn, Amy C"

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  1. 1

    Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy by Van Bergen, Nicole J, Crowston, Jonathan G, Kearns, Lisa S, Staffieri, Sandra E, Hewitt, Alex W, Cohn, Amy C, Mackey, David A, Trounce, Ian A

    Published in PloS one (22-06-2011)
    “…Autosomal Dominant Optic Atrophy (ADOA) is the most common inherited optic atrophy where vision impairment results from specific loss of retinal ganglion cells…”
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    Journal Article
  2. 2

    Orbital cavernous venous malformation shrinkage during fractionated stereotactic radiotherapy contributing to the development of radiation retinopathy by Hughes, Laura, Cohn, Amy C, Haghighi, Neda, McNab, Alan A

    Published in European journal of ophthalmology (01-09-2024)
    “…Background Posterior movement of ocular tissue secondary to orbital cavernous venous malformation shrinkage from fractionated stereotactic radiotherapy can…”
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  3. 3

    Clinical performance of predicting late age‐related macular degeneration development using multimodal imaging by Goh, Kai Lyn, Abbott, Carla J., Campbell, Thomas G., Cohn, Amy C., Ong, Dai Ni, Wickremasinghe, Sanjeewa S., Hodgson, Lauren A. B., Guymer, Robyn H., Wu, Zhichao

    Published in Clinical & experimental ophthalmology (01-09-2024)
    “…Background To examine whether the clinical performance of predicting late age‐related macular degeneration (AMD) development is improved through using…”
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  4. 4

    Subthreshold Nano-Second Laser Treatment and Age-Related Macular Degeneration by Cohn, Amy C, Wu, Zhichao, Jobling, Andrew I, Fletcher, Erica L, Guymer, Robyn H

    Published in Journal of clinical medicine (28-01-2021)
    “…The presence of drusen is an important hallmark of age-related macular degeneration (AMD). Laser-induced regression of drusen, first observed over four decades…”
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  5. 5

    Autosomal Dominant Optic Atrophy: Penetrance and Expressivity in Patients With OPA1 Mutations by Cohn, Amy C, Toomes, Carmel, Potter, Catherine, Towns, Katherine V, Hewitt, Alex W, Inglehearn, Chris F, Craig, Jamie E, Mackey, David A

    Published in American journal of ophthalmology (01-04-2007)
    “…Purpose We identified families with autosomal dominant optic atrophy (ADOA), determined the number and type of OPA1 mutations, and investigated the phenotypic…”
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    Journal Article
  6. 6

    Younger Siblings, C-Reactive Protein, and Risk of Age-Related Macular Degeneration by COHN, Amy C, BUSIJA, Lucy, ROBMAN, Liubov D, DIMITROV, Peter N, VARSAMIDIS, Mary, LIM, Lyndell L, BAIRD, Paul N, GUYMER, Robyn H

    Published in American journal of epidemiology (01-05-2013)
    “…In this study, we examined the relationship between exposure to siblings and 1) the risk of age-related macular degeneration (AMD) and 2) C-reactive protein…”
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  7. 7

    Current advances in multimodal imaging in geographic atrophy secondary to age-related macular degeneration: A review by Cohn, Amy C., Guymer, Robyn H.

    Published in Taiwan journal of ophthalmology (06-11-2024)
    “…As we move toward an era in which there will be treatment options for geographic atrophy (GA) secondary to age-related macular degeneration, the need to…”
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  8. 8

    Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome by Cohn, Amy C, Kotschet, Katya, Veitch, Alistair, Delatycki, Martin B, McCombe, Mark F

    Published in Clinical & experimental ophthalmology (01-04-2005)
    “…The ophthalmic features are reported of a member of an Australian pedigree with three affected individuals spanning two generations with a hereditary…”
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  9. 9

    Does acute loss of vision in Autosomal Dominant Optic Atrophy occur early in childhood? by Kearns, Lisa S., Forrest, Michael, Cohn, Amy C., Churchill, Amanda J., Mackey, David A

    Published in Ophthalmic genetics (01-03-2010)
    “…Purpose: In contrast to Autosomal dominant optic atrophy (ADOA), acute loss of vision is normally observed in Leber's hereditary optic neuropathy (LHON)…”
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    Journal Article
  10. 10

    Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy 8q22-Qter/ Monosomy 9p23-Pter by Cohn, Amy C., Kearns, Lisa S., Savarirayan, Ravi, Ryan, Jacinta, Craig, Jamie E., Mackey, David A.

    Published in Ophthalmic genetics (01-03-2005)
    “…Purpose: To present a case of congenital glaucoma with an unbalanced translocation trisomy 8q22-qter/monosomy 9p23-pter, resulting in trisomy of the GLC1D…”
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    Journal Article
  11. 11

    Subthreshold Nanosecond Laser in Age-Related Macular Degeneration: Observational Extension Study of the LEAD Clinical Trial by Guymer, Robyn H, Chen, Fred K, Hodgson, Lauren A B, Caruso, Emily, Harper, Colin A, Wickremashinghe, Sanjeewa S, Cohn, Amy C, Sivarajah, Pyrawy, Tindill, Nicole, Luu, Chi D, Wu, Zhichao

    Published in Ophthalmology retina (01-12-2021)
    “…To evaluate the long-term effect of subthreshold nanosecond laser (SNL) treatment on progression to late age-related macular degeneration (AMD). Observational…”
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    Journal Article
  12. 12

    Autosomal Dominant Optic Atrophy: Penetrance and Expressivity in Patients WithOPA1Mutations by Cohn, Amy C, Toomes, Carmel, Potter, Catherine, Towns, Katherine V, Hewitt, Alex W, Inglehearn, Chris F, Craig, Jamie E, Mackey, David A

    Published in American journal of ophthalmology (01-04-2007)
    “…Purpose We identified families with autosomal dominant optic atrophy (ADOA), determined the number and type ofOPA1mutations, and investigated the phenotypic…”
    Get full text
    Journal Article
  13. 13