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Anthony T Moore

Showing results (91-100 of 277) with videos related to

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Investigative Ophthalmology & Visual Science|January 27, 2017
The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity LossesAnna Majander, Catarina João, Andrew T Rider, et al.
Retinal Cases & Brief Reports|August 4, 2018
PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCYMariana A Flores Pimentel, Irina De la Huerta, Jacque L Duncan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Ophthalmology|October 13, 2009
Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia)Michel Michaelides, Zheng Li, Naheed A Rana, et al.
Ophthalmic Genetics|November 29, 2016
Vitamin A deficiency due to bi-allelic mutation of RBP4: There's more to it than meets the eyeKamron N Khan, Keren Carss, F Lucy Raymond, et al.
Investigative Ophthalmology & Visual Science|September 2, 2016
Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4Ana Fakin, Anthony G Robson, Kaoru Fujinami, et al.
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.
Ophthalmology|November 9, 2013
Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutationEva Lenassi, Zubin Saihan, Valentina Cipriani, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
Progressive cone dystrophy associated with mutation in CNGB3Michel Michaelides, Irene A Aligianis, John R Ainsworth, 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.
Pageof 28

Showing results (91-100 of 277) with videos related to

Sort By:
Pageof 28
Investigative Ophthalmology & Visual Science|January 27, 2017
The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity LossesAnna Majander, Catarina João, Andrew T Rider, et al.
Retinal Cases & Brief Reports|August 4, 2018
PHENOTYPIC HETEROGENEITY IN A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH PREVENTION OF VISUAL LOSS IN AN AFFECTED MALE CHILD WITH LASER TREATMENT IN INFANCYMariana A Flores Pimentel, Irina De la Huerta, Jacque L Duncan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Ophthalmology|October 13, 2009
Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia)Michel Michaelides, Zheng Li, Naheed A Rana, et al.
Ophthalmic Genetics|November 29, 2016
Vitamin A deficiency due to bi-allelic mutation of RBP4: There's more to it than meets the eyeKamron N Khan, Keren Carss, F Lucy Raymond, et al.
Investigative Ophthalmology & Visual Science|September 2, 2016
Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4Ana Fakin, Anthony G Robson, Kaoru Fujinami, et al.
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.
Ophthalmology|November 9, 2013
Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutationEva Lenassi, Zubin Saihan, Valentina Cipriani, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
Progressive cone dystrophy associated with mutation in CNGB3Michel Michaelides, Irene A Aligianis, John R Ainsworth, 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.
Pageof 28