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Alice E Davidson

Showing results (1-10 of 66) with videos related to

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BMJ Open Ophthalmology|September 26, 2022
Fuchs endothelial corneal dystrophy: current perspectives on diagnostic pathology and genetics-Bowman Club LectureCaroline Thaung, Alice E Davidson
Cornea|April 6, 2019
Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3Lubica Dudakova, Pavlina Skalicka, Alice E Davidson, et al.
Progress in Retinal and Eye Research|November 24, 2025
Pathological mechanism in Fuchs endothelial corneal dystrophy and myotonic dystrophy type 1: more than meets the eyeElisa Landi, Derick G Wansink, Vanessa LaPointe, et al.
Acta Ophthalmologica|October 14, 2025
Exploring the histopathological signature of repeat-mediated Fuchs endothelial corneal dystrophyAnne-Marie S Kladny, Nihar Bhattacharyya, Marcos Abreu Costa, et al.
Ophthalmology|December 21, 2011
Retinal structure, function, and molecular pathologic features in gyrate atrophyPanagiotis I Sergouniotis, Alice E Davidson, Eva Lenassi, et al.
Journal of Clinical Medicine|September 9, 2022
Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel <i>FOXC1</i> VariantPavlina Skalicka, Jana Jedlickova, Ales Horinek, et al.
Investigative Ophthalmology & Visual Science|December 10, 2015
Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital AmaurosisJames Bellingham, Alice E Davidson, Jonathan Aboshiha, et al.
Ophthalmic Research|December 16, 2014
Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutationPetra Liskova, Lubica Dudakova, Vladimir Tesar, et al.
American Journal of Human Genetics|July 19, 2011
Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosisPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
FEBS Letters|June 22, 2011
The cataract-associated protein TMEM114, and TMEM235, are glycosylated transmembrane proteins that are distinct from claudin family membersGeoffrey J Maher, Emma N Hilton, Jill E Urquhart, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
BMJ Open Ophthalmology|September 26, 2022
Fuchs endothelial corneal dystrophy: current perspectives on diagnostic pathology and genetics-Bowman Club LectureCaroline Thaung, Alice E Davidson
Cornea|April 6, 2019
Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3Lubica Dudakova, Pavlina Skalicka, Alice E Davidson, et al.
Progress in Retinal and Eye Research|November 24, 2025
Pathological mechanism in Fuchs endothelial corneal dystrophy and myotonic dystrophy type 1: more than meets the eyeElisa Landi, Derick G Wansink, Vanessa LaPointe, et al.
Acta Ophthalmologica|October 14, 2025
Exploring the histopathological signature of repeat-mediated Fuchs endothelial corneal dystrophyAnne-Marie S Kladny, Nihar Bhattacharyya, Marcos Abreu Costa, et al.
Ophthalmology|December 21, 2011
Retinal structure, function, and molecular pathologic features in gyrate atrophyPanagiotis I Sergouniotis, Alice E Davidson, Eva Lenassi, et al.
Journal of Clinical Medicine|September 9, 2022
Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel <i>FOXC1</i> VariantPavlina Skalicka, Jana Jedlickova, Ales Horinek, et al.
Investigative Ophthalmology & Visual Science|December 10, 2015
Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital AmaurosisJames Bellingham, Alice E Davidson, Jonathan Aboshiha, et al.
Ophthalmic Research|December 16, 2014
Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutationPetra Liskova, Lubica Dudakova, Vladimir Tesar, et al.
American Journal of Human Genetics|July 19, 2011
Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosisPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
FEBS Letters|June 22, 2011
The cataract-associated protein TMEM114, and TMEM235, are glycosylated transmembrane proteins that are distinct from claudin family membersGeoffrey J Maher, Emma N Hilton, Jill E Urquhart, et al.
Pageof 7