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Showing results (901-910 of 1,250) with videos related to

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The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
Retina (Philadelphia, Pa.)|April 14, 2011
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing lossZubin Saihan, Polona Le Quesne Stabej, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Nature Biomedical Engineering|March 30, 2022
Detection of signs of disease in external photographs of the eyes via deep learningBoris Babenko, Akinori Mitani, Ilana Traynis, et al.
Translational Vision Science & Technology|December 11, 2023
Risk Stratification for Diabetic Retinopathy Screening Order Using Deep Learning: A Multicenter Prospective StudyAshish Bora, Richa Tiwari, Pinal Bavishi, et al.
American Journal of Ophthalmology|November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female CarriersMichalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.
Pageof 125

Showing results (901-910 of 1,250) with videos related to

Sort By:
Pageof 125
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
Retina (Philadelphia, Pa.)|April 14, 2011
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing lossZubin Saihan, Polona Le Quesne Stabej, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Nature Biomedical Engineering|March 30, 2022
Detection of signs of disease in external photographs of the eyes via deep learningBoris Babenko, Akinori Mitani, Ilana Traynis, et al.
Translational Vision Science & Technology|December 11, 2023
Risk Stratification for Diabetic Retinopathy Screening Order Using Deep Learning: A Multicenter Prospective StudyAshish Bora, Richa Tiwari, Pinal Bavishi, et al.
American Journal of Ophthalmology|November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female CarriersMichalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Journal of Medical Genetics|November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataractsA Arora, P J Minogue, X Liu, et al.
The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.
Pageof 125