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Orbit (Amsterdam, Netherlands)
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March 11, 2006
Severe, unstable migraine: a risk factor for postoperative ophthalmic artery spasm?
Jodhbir S Mehta, Adam Gajdatsy, Andrew R Webster, et al.
Ophthalmic Genetics
|
June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophy
Giovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
American Journal of Ophthalmology
|
March 22, 2017
Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy
James J L Tee, Joseph Carroll, Andrew R Webster, et al.
Eye (London, England)
|
May 17, 2018
Retinal findings in a patient with mutations in ABCC6 and ABCA4
Omar A Mahroo, Kaoru Fujinami, Anthony T Moore, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
July 13, 2011
Unilateral retinitis pigmentosa occurring in an individual with a germline mutation in the RP1 gene
Rajarshi Mukhopadhyay, Graham E Holder, Anthony T Moore, et al.
American Journal of Medical Genetics. Part A
|
July 11, 2024
Unveiling hidden genetic complexity: Coexistence of HGSNAT and EYS variants in a patient with retinal dystrophy
Siying Lin, Elena Schiff, Gavin Arno, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
September 14, 2017
Quantitative and Qualitative Features of Spectral-Domain Optical Coherence Tomography Provide Prognostic Indicators for Visual Acuity in Patients With Choroideremia
Alessandro Abbouda, Wei Sing Lim, Lina Sprogyte, et al.
Experimental Eye Research
|
January 10, 2017
Mechanism and evidence of nonsense suppression therapy for genetic eye disorders
Rose Richardson, Matthew Smart, Dhani Tracey-White, et al.
Ophthalmic Genetics
|
August 2, 2024
Mild retinitis pigmentosa, including sector retinitis pigmentosa associated with 2 pathogenic variants in <i>CDH23</i>
Pankaja Dhoble, Thales A C de Guimarães, Andrew R Webster, et al.
Ophthalmic Genetics
|
May 8, 2019
Rod-cone dystrophy associated with the Gly167Asp variant in PRPH2
Rola Ba-Abbad, Anthony G Robson, Becky MacPhee, et al.
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of 38
Search research articles
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Showing results (11-20 of 372) with videos related to
Sort By:
Page
of 38
Orbit (Amsterdam, Netherlands)
|
March 11, 2006
Severe, unstable migraine: a risk factor for postoperative ophthalmic artery spasm?
Jodhbir S Mehta, Adam Gajdatsy, Andrew R Webster, et al.
Ophthalmic Genetics
|
June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophy
Giovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
American Journal of Ophthalmology
|
March 22, 2017
Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy
James J L Tee, Joseph Carroll, Andrew R Webster, et al.
Eye (London, England)
|
May 17, 2018
Retinal findings in a patient with mutations in ABCC6 and ABCA4
Omar A Mahroo, Kaoru Fujinami, Anthony T Moore, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
July 13, 2011
Unilateral retinitis pigmentosa occurring in an individual with a germline mutation in the RP1 gene
Rajarshi Mukhopadhyay, Graham E Holder, Anthony T Moore, et al.
American Journal of Medical Genetics. Part A
|
July 11, 2024
Unveiling hidden genetic complexity: Coexistence of HGSNAT and EYS variants in a patient with retinal dystrophy
Siying Lin, Elena Schiff, Gavin Arno, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
September 14, 2017
Quantitative and Qualitative Features of Spectral-Domain Optical Coherence Tomography Provide Prognostic Indicators for Visual Acuity in Patients With Choroideremia
Alessandro Abbouda, Wei Sing Lim, Lina Sprogyte, et al.
Experimental Eye Research
|
January 10, 2017
Mechanism and evidence of nonsense suppression therapy for genetic eye disorders
Rose Richardson, Matthew Smart, Dhani Tracey-White, et al.
Ophthalmic Genetics
|
August 2, 2024
Mild retinitis pigmentosa, including sector retinitis pigmentosa associated with 2 pathogenic variants in <i>CDH23</i>
Pankaja Dhoble, Thales A C de Guimarães, Andrew R Webster, et al.
Ophthalmic Genetics
|
May 8, 2019
Rod-cone dystrophy associated with the Gly167Asp variant in PRPH2
Rola Ba-Abbad, Anthony G Robson, Becky MacPhee, et al.
Page
of 38