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Anthony G Robson

Showing results (81-90 of 188) with videos related to

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Investigative Ophthalmology & Visual Science|November 8, 2016
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous PatientsAna Fakin, Anthony G Robson, John Pei-Wen Chiang, et al.
Human Molecular Genetics|July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypesYuri V Sergeev, Susan Vitale, Paul A Sieving, et al.
Investigative Ophthalmology & Visual Science|February 19, 2025
Clinical, Genetic, Imaging and Electrophysiological Findings in a Cohort of Patients With GUCA1A-Associated RetinopathyGilad Allon, Siying Lin, Anthony G Robson, et al.
The British Journal of Ophthalmology|May 25, 2021
Novel disease-causing variant in <i>RDH12</i> presenting with autosomal dominant retinitis pigmentosaManickam Nick Muthiah, Angelos Kalitzeos, Kate Oprych, et al.
Retina (Philadelphia, Pa.)|June 28, 2017
ELECTROPHYSIOLOGICAL CHARACTERIZATION OF MACULAR TELANGIECTASIA TYPE 2 AND STRUCTURE-FUNCTION CORRELATIONMali Okada, Anthony G Robson, Catherine A Egan, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Eye (London, England)|July 19, 2020
A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophyRola Ba-Abbad, Anthony G Robson, Omar A Mahroo, et al.
Molecular Vision|April 21, 2010
Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathyEsther Meyer, Michel Michaelides, Louise J Tee, et al.
American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
Pageof 19

Showing results (81-90 of 188) with videos related to

Sort By:
Pageof 19
Investigative Ophthalmology & Visual Science|November 8, 2016
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous PatientsAna Fakin, Anthony G Robson, John Pei-Wen Chiang, et al.
Human Molecular Genetics|July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypesYuri V Sergeev, Susan Vitale, Paul A Sieving, et al.
Investigative Ophthalmology & Visual Science|February 19, 2025
Clinical, Genetic, Imaging and Electrophysiological Findings in a Cohort of Patients With GUCA1A-Associated RetinopathyGilad Allon, Siying Lin, Anthony G Robson, et al.
The British Journal of Ophthalmology|May 25, 2021
Novel disease-causing variant in <i>RDH12</i> presenting with autosomal dominant retinitis pigmentosaManickam Nick Muthiah, Angelos Kalitzeos, Kate Oprych, et al.
Retina (Philadelphia, Pa.)|June 28, 2017
ELECTROPHYSIOLOGICAL CHARACTERIZATION OF MACULAR TELANGIECTASIA TYPE 2 AND STRUCTURE-FUNCTION CORRELATIONMali Okada, Anthony G Robson, Catherine A Egan, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Eye (London, England)|July 19, 2020
A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophyRola Ba-Abbad, Anthony G Robson, Omar A Mahroo, et al.
Molecular Vision|April 21, 2010
Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathyEsther Meyer, Michel Michaelides, Louise J Tee, et al.
American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
Pageof 19