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G Robson

Showing results (321-330 of 456) with videos related to

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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.
The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, 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.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
American Journal of Ophthalmology|March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural HistorySagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Ophthalmology|October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical TrialsGiuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2001
Accelerated nephrotoxic nephritis is exacerbated in C1q-deficient miceM G Robson, H T Cook, M Botto, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Pageof 46

Showing results (321-330 of 456) with videos related to

Sort By:
Pageof 46
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.
The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, 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.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
American Journal of Ophthalmology|March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural HistorySagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Ophthalmology|October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical TrialsGiuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2001
Accelerated nephrotoxic nephritis is exacerbated in C1q-deficient miceM G Robson, H T Cook, M Botto, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Pageof 46