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Physics in Medicine and Biology
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January 22, 2010
Radio frequency shielding for a linac-MRI system
M Lamey, B Burke, E Blosser, et al.
Clinical & Experimental Ophthalmology
|
April 28, 2015
Genetic analysis of choroideremia families in the Australian population
Terri L McLaren, John N De Roach, Hannah Montgomery, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 18, 2024
Non-syndromic OTX2-associated pattern dystrophy: a 10-year multimodal imaging study
Prathiba Ramakrishnan, Matthew K Kenworthy, Jonathan A Alexis, et al.
Molecular Vision
|
August 10, 2012
Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa
Rachel L Paterson, John N De Roach, Terri L McLaren, et al.
Ophthalmology Science
|
September 16, 2024
Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline
Jason Charng, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Molecular Vision
|
August 10, 2018
Maternal uniparental isodisomy of chromosome 6 unmasks a novel variant in <i>TULP1</i> in a patient with early onset retinal dystrophy
Emmanuelle Souzeau, Jennifer A Thompson, Terri L McLaren, et al.
Ophthalmic Genetics
|
April 16, 2026
Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathy
Roselind L Ni, Rebecca Procopio, Ezann Siebert, et al.
The CRISPR Journal
|
April 5, 2024
Rapid Variant Pathogenicity Analysis by CRISPR Activation of <i>CRB1</i> Gene Expression in Patient-Derived Fibroblasts
Sang Yoon Moon, Dan Zhang, Shang-Chih Chen, et al.
Clinical & Experimental Ophthalmology
|
April 21, 2015
Clinical and molecular characterization of females affected by X-linked retinoschisis
Sandra E Staffieri, Loreto Rose, Andrew Chang, et al.
Stem Cell Research
|
April 12, 2025
Generation of the induced pluripotent stem cell line LEIi023-A from a rod-cone dystrophy patient carrying the dominant PRPF31 c.267del variant
Dan Zhang, Di Huang, Shang-Chih Chen, et al.
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Search research articles
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Showing results (11-20 of 73) with videos related to
Sort By:
Page
of 8
Physics in Medicine and Biology
|
January 22, 2010
Radio frequency shielding for a linac-MRI system
M Lamey, B Burke, E Blosser, et al.
Clinical & Experimental Ophthalmology
|
April 28, 2015
Genetic analysis of choroideremia families in the Australian population
Terri L McLaren, John N De Roach, Hannah Montgomery, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
July 18, 2024
Non-syndromic OTX2-associated pattern dystrophy: a 10-year multimodal imaging study
Prathiba Ramakrishnan, Matthew K Kenworthy, Jonathan A Alexis, et al.
Molecular Vision
|
August 10, 2012
Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa
Rachel L Paterson, John N De Roach, Terri L McLaren, et al.
Ophthalmology Science
|
September 16, 2024
Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline
Jason Charng, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Molecular Vision
|
August 10, 2018
Maternal uniparental isodisomy of chromosome 6 unmasks a novel variant in <i>TULP1</i> in a patient with early onset retinal dystrophy
Emmanuelle Souzeau, Jennifer A Thompson, Terri L McLaren, et al.
Ophthalmic Genetics
|
April 16, 2026
Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathy
Roselind L Ni, Rebecca Procopio, Ezann Siebert, et al.
The CRISPR Journal
|
April 5, 2024
Rapid Variant Pathogenicity Analysis by CRISPR Activation of <i>CRB1</i> Gene Expression in Patient-Derived Fibroblasts
Sang Yoon Moon, Dan Zhang, Shang-Chih Chen, et al.
Clinical & Experimental Ophthalmology
|
April 21, 2015
Clinical and molecular characterization of females affected by X-linked retinoschisis
Sandra E Staffieri, Loreto Rose, Andrew Chang, et al.
Stem Cell Research
|
April 12, 2025
Generation of the induced pluripotent stem cell line LEIi023-A from a rod-cone dystrophy patient carrying the dominant PRPF31 c.267del variant
Dan Zhang, Di Huang, Shang-Chih Chen, et al.
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of 8