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Gavin Arno

Showing results (31-40 of 185) with videos related to

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Ophthalmic Genetics|May 22, 2025
<i>DYRK1A</i> syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotypeSiying Lin, Eleanor Hay, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Clinical Science (London, England : 1979)|February 14, 2004
Quantification of mitochondrial sublimons in human fibrillating atriaNidal Maarouf, Gavin Arno, Nicholas D Carter, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 4, 2008
Differential pathways govern CD4+ CD28- T cell proinflammatory and effector responses in patients with coronary artery diseaseBehnam Zal, Juan C Kaski, Julius P Akiyu, et al.
NPJ Genomic Medicine|December 20, 2024
Functional assessment of IDUA variants of uncertain significance identified by newborn screeningSeok-Ho Yu, Francyne Kubaski, Gavin Arno, et al.
Human Mutation|July 28, 2007
The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutationsPaolo Comeglio, Philip Johnson, Gavin Arno, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Eye (London, England)|December 5, 2024
Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathySiying Lin, Gavin Arno, Anthony G Robson, 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.
Pageof 19

Showing results (31-40 of 185) with videos related to

Sort By:
Pageof 19
Ophthalmic Genetics|May 22, 2025
<i>DYRK1A</i> syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotypeSiying Lin, Eleanor Hay, Dorothy A Thompson, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Clinical Science (London, England : 1979)|February 14, 2004
Quantification of mitochondrial sublimons in human fibrillating atriaNidal Maarouf, Gavin Arno, Nicholas D Carter, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 4, 2008
Differential pathways govern CD4+ CD28- T cell proinflammatory and effector responses in patients with coronary artery diseaseBehnam Zal, Juan C Kaski, Julius P Akiyu, et al.
NPJ Genomic Medicine|December 20, 2024
Functional assessment of IDUA variants of uncertain significance identified by newborn screeningSeok-Ho Yu, Francyne Kubaski, Gavin Arno, et al.
Human Mutation|July 28, 2007
The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutationsPaolo Comeglio, Philip Johnson, Gavin Arno, et al.
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Eye (London, England)|December 5, 2024
Bifocal retinal degeneration observed on ultra-widefield autofluorescence in some cases of CRX-associated retinopathySiying Lin, Gavin Arno, Anthony G Robson, 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.
Pageof 19