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Anthony T Moore

Showing results (111-120 of 277) with videos related to

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American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
Neuroimage|December 20, 2003
Quantitative MR image analysis in subjects with defects in the PAX6 geneSamantha L Free, Tejal N Mitchell, Kathleen A Williamson, et al.
The Laryngoscope|October 28, 2020
Genetic Testing Leading to Early Identification of Childhood Ocular Manifestations of Usher SyndromeKara D Brodie, Anthony T Moore, Anne M Slavotinek, et al.
Genes|June 27, 2024
Enhanced Learning and Memory in Patients with <i>CRB1</i> RetinopathyGenevieve A Wright, Ana Catalina Rodriguez-Martinez, Hanne Conn, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, 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.
Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
The British Journal of Ophthalmology|June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophiesRyan Combs, Georgina Hall, Katherine Payne, et al.
American Journal of Ophthalmology|September 7, 2015
Retinal Architecture in ​RGS9- and ​R9AP-Associated Retinal Dysfunction (Bradyopsia)Rupert W Strauss, Adam M Dubis, Robert F Cooper, et al.
Investigative Ophthalmology & Visual Science|August 10, 2022
Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1Maria Pilar Martin-Gutierrez, Elena R Schiff, Genevieve Wright, et al.
Pageof 28

Showing results (111-120 of 277) with videos related to

Sort By:
Pageof 28
American Journal of Ophthalmology|June 12, 2016
Unilateral BEST1-Associated RetinopathyRashi Arora, Kamron Khan, Melissa L Kasilian, et al.
Neuroimage|December 20, 2003
Quantitative MR image analysis in subjects with defects in the PAX6 geneSamantha L Free, Tejal N Mitchell, Kathleen A Williamson, et al.
The Laryngoscope|October 28, 2020
Genetic Testing Leading to Early Identification of Childhood Ocular Manifestations of Usher SyndromeKara D Brodie, Anthony T Moore, Anne M Slavotinek, et al.
Genes|June 27, 2024
Enhanced Learning and Memory in Patients with <i>CRB1</i> RetinopathyGenevieve A Wright, Ana Catalina Rodriguez-Martinez, Hanne Conn, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, 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.
Genomics|March 28, 2003
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)Samantha Johnson, Stephanie Halford, Alex G Morris, et al.
The British Journal of Ophthalmology|June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophiesRyan Combs, Georgina Hall, Katherine Payne, et al.
American Journal of Ophthalmology|September 7, 2015
Retinal Architecture in ​RGS9- and ​R9AP-Associated Retinal Dysfunction (Bradyopsia)Rupert W Strauss, Adam M Dubis, Robert F Cooper, et al.
Investigative Ophthalmology & Visual Science|August 10, 2022
Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1Maria Pilar Martin-Gutierrez, Elena R Schiff, Genevieve Wright, et al.
Pageof 28