Risultati della ricerca - Grigg, John R.

Cataract Surgery in Short Eyes, Including Nanophthalmos: Visual Outcomes, Complications and Refractive Results di Yosar, Jason C, Zagora, Sophia L, Grigg, John R

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The electroretinogram in the genomics era: outer retinal disorders di Cornish, Elisa E., Vaze, Anagha, Jamieson, Robyn V., Grigg, John R.

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Idiopathic full thickness macular hole in a 10-year-old girl di Lim, Li-Anne S., Fernandez-Sanz, Guillermo, Levasseur, Steven, Grigg, John R., Hunyor, Alex P.

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Barriers and facilitators to diabetic retinopathy screening within Australian primary care di Watson, Matthew J. G., McCluskey, Peter J., Grigg, John R., Kanagasingam, Yogesan, Daire, Judith, Estai, Mohamed

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NMNAT1 variants cause cone and cone-rod dystrophy di Nash, Benjamin M., Symes, Richard, Goel, Himanshu, Dinger, Marcel E., Bennetts, Bruce, Grigg, John R., Jamieson, Robyn V.

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Comparison of perimetric Glaucoma Staging Systems in Asians with primary glaucoma di Hoang, Tung Thanh, Van Bui, Anh, Nguyen, Vuong, McCluskey, Peter J., Grigg, John R., Skalicky, Simon Edward

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Response to: “Comment on: ‘Comparison of perimetric glaucoma staging systems in Asians with primary glaucoma’” di Hoang, Tung Thanh, Van Bui, Anh, Nguyen, Vuong, McCluskey, Peter J., Grigg, John R., Skalicky, Simon Edward

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Outcome measures in juvenile X-linked retinoschisis: A systematic review di Grigg, John R., Hooper, Claire Y., Fraser, Clare L., Cornish, Elisa E., McCluskey, Peter J., Jamieson, Robyn V.

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Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1 di Prokudin, Ivan, Simons, Cas, Grigg, John R, Storen, Rebecca, Kumar, Vikrant, Phua, Zai Y, Smith, James, Flaherty, Maree, Davila, Sonia, Jamieson, Robyn V

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Central corneal thickness changes and horizontal corneal diameter in premature infants: A prospective analysis di Choo, May May, Yeong, Choo Mee, Grigg, John R., Khaliddin, Nurliza, Kadir, Azida Juana, Barnes, Elizabeth H., Kamalden, Tengku Ain, Watson, Stephanie L.

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Assessing Residual Cone Function in Retinitis Pigmentosa Patients di Arsiwalla, Tasneem A., Cornish, Elisa E., Nguyen, Phuc Vuong, Korsakova, Maria, Ali, Haipha, Saakova, Nonna, Fraser, Clare L., Jamieson, Robyn V., Grigg, John R.

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Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic RPGR Variant Assessment for Therapy Suitability di Chahine Karam, Fidelle, Loi, To Ha, Ma, Alan, Nash, Benjamin M., Grigg, John R., Parekh, Darshan, Riley, Lisa G., Farnsworth, Elizabeth, Bennetts, Bruce, Gonzalez-Cordero, Anai, Jamieson, Robyn V.

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Novel SOX2 partner-factor domain mutation in a four-generation family di Mihelec, Marija, Abraham, Peter, Gibson, Kate, Krowka, Renata, Susman, Rachel, Storen, Rebecca, Chen, Yongjuan, Donald, Jenny, Tam, Patrick PL, Grigg, John R, Flaherty, Maree, Gole, Glen A, Jamieson, Robyn V

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Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells di Nash, Benjamin M., Loi, To Ha, Fernando, Milan, Sabri, Amin, Robinson, James, Cheng, Anson, Eamegdool, Steven S., Farnsworth, Elizabeth, Bennetts, Bruce, Grigg, John R., Chung, Seo-Kyung, Gonzalez-Cordero, Anai, Jamieson, Robyn V.

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Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachment di Nash, Benjamin M., Watson, Christopher J. G., Hughes, Edward, Hou, Alec L., Loi, To Ha, Bennetts, Bruce, Jelovic, Diana, Polkinghorne, Philip J., Gorbatov, Mark, Grigg, John R., Vincent, Andrea L., Jamieson, Robyn V.

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UVEITIS CAUSED BY TREATMENT FOR MALIGNANT MELANOMA: A CASE SERIES di Whist, Eline, Symes, Richard J., Chang, John H., Chowdhury, Vivek, Lim, Li-Anne, Grigg, John R., Lin, Ming-Lee, Karaconji, Tanya, Giblin, Michael, Symons, Andrew, Lim, Lyndell L., McCluskey, Peter J.

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Efficient capture of high-quality real-world data on treatments for glaucoma: the Fight Glaucoma Blindness! Registry di Lawlor, Mitchell, Nguyen, Vuong, Brooks, Anne, Clement, Colin, Craig, Jamie E, Danesh-Meyer, Helen, Goldberg, Ivan, Graham, Stuart L, Grigg, John R, Howes, Frank, Lim, Ridia, Skalicky, Simon E, White, Andrew J, Gillies, Mark

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Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing di Ma, Alan S., Grigg, John R., Ho, Gladys, Prokudin, Ivan, Farnsworth, Elizabeth, Holman, Katherine, Cheng, Anson, Billson, Frank A., Martin, Frank, Fraser, Clare, Mowat, David, Smith, James, Christodoulou, John, Flaherty, Maree, Bennetts, Bruce, Jamieson, Robyn V.

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Electrophysiological Assessment in Birdshot Chorioretinopathy: Flicker Electroretinograms Recorded With a Handheld Device di Waldie, Anna M., Hobby, Angharad E., Chow, Isabelle, Cornish, Elisa E., Indusegaran, Mathura, Pekacka, Aleksandra, Nguyen, Phuc, Fraser, Clare, Binns, Alison M., Stanford, Miles R., Hammond, Christopher J., McCluskey, Peter J., Grigg, John R., Mahroo, Omar A.

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Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies di Nash, Benjamin M., Ma, Alan, Ho, Gladys, Farnsworth, Elizabeth, Minoche, Andre E., Cowley, Mark J., Barnett, Christopher, Smith, Janine M., Loi, To Ha, Wong, Karen, St Heaps, Luke, Wright, Dale, Dinger, Marcel E., Bennetts, Bruce, Grigg, John R., Jamieson, Robyn V.

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