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Anthony G Robson

Showing results (111-120 of 188) with videos related to

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Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, 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.
Progress in Retinal and Eye Research|January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromesMichalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Pageof 19

Showing results (111-120 of 188) with videos related to

Sort By:
Pageof 19
Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
American Journal of Ophthalmology|September 13, 2022
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural HistoryMalena Daich Varela, Michalis Georgiou, Yahya Alswaiti, et al.
Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, 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.
Progress in Retinal and Eye Research|January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromesMichalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Pageof 19