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Gavin Arno

Showing results (81-90 of 185) with videos related to

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Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Scientific Reports|August 10, 2017
Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locusValentina Cipriani, Raquel S Silva, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Investigative Ophthalmology & Visual Science|May 3, 2024
Sex Distributions in Non-ABCA4 Autosomal Macular DystrophiesAmit V Mishra, Sandra Vermeirsch, Siying Lin, et al.
Disease Models & Mechanisms|January 26, 2026
Enhanced lysosomal exocytosis and altered growth factor signaling are associated with cartilage pathology in a zebrafish model of MPSIVAJen-Jie Lee, Po-Nien Lu, Lynn Dukes-Rimsky, et al.
Clinical Genetics|June 12, 2024
Non-syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activitySiying Lin, Anthony G Robson, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
JAMA Ophthalmology|June 4, 2016
Molecular and Clinical Findings in Patients With Knobloch SyndromeSarah Hull, Gavin Arno, Cristy A Ku, et al.
American Journal of Human Genetics|May 6, 2014
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophyPanagiotis I Sergouniotis, Christina Chakarova, Cian Murphy, et al.
JAMA Ophthalmology|May 31, 2014
Expansion of ocular phenotypic features associated with mutations in ADAMTS18Aman Chandra, Gavin Arno, Kathleen Williamson, et al.
Pageof 19

Showing results (81-90 of 185) with videos related to

Sort By:
Pageof 19
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Scientific Reports|August 10, 2017
Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locusValentina Cipriani, Raquel S Silva, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Investigative Ophthalmology & Visual Science|May 3, 2024
Sex Distributions in Non-ABCA4 Autosomal Macular DystrophiesAmit V Mishra, Sandra Vermeirsch, Siying Lin, et al.
Disease Models & Mechanisms|January 26, 2026
Enhanced lysosomal exocytosis and altered growth factor signaling are associated with cartilage pathology in a zebrafish model of MPSIVAJen-Jie Lee, Po-Nien Lu, Lynn Dukes-Rimsky, et al.
Clinical Genetics|June 12, 2024
Non-syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activitySiying Lin, Anthony G Robson, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
JAMA Ophthalmology|June 4, 2016
Molecular and Clinical Findings in Patients With Knobloch SyndromeSarah Hull, Gavin Arno, Cristy A Ku, et al.
American Journal of Human Genetics|May 6, 2014
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophyPanagiotis I Sergouniotis, Christina Chakarova, Cian Murphy, et al.
JAMA Ophthalmology|May 31, 2014
Expansion of ocular phenotypic features associated with mutations in ADAMTS18Aman Chandra, Gavin Arno, Kathleen Williamson, et al.
Pageof 19