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Eva Lenassi

Showing results (11-20 of 30) with videos related to

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The American Journal of Pathology|June 11, 2013
Complement component C3 plays a critical role in protecting the aging retina in a murine model of age-related macular degenerationJaimie Hoh Kam, Eva Lenassi, Talat H Malik, et al.
Journal of Neurology|December 12, 2024
A rare cause of autosomal recessive ataxia with very late diagnosis and prolonged disease courseShakya Bhattacharjee, Eva Lenassi, Robert W Taylor, et al.
JAMA Ophthalmology|December 19, 2014
Clinical heterogeneity in a family with mutations in USH2AEva Lenassi, Anthony G Robson, Linda M Luxon, et al.
American Journal of Ophthalmology|October 6, 2012
Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1)Eva Lenassi, Eric Troeger, Robert Wilke, 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.
Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Investigative Ophthalmology & Visual Science|June 14, 2021
North Carolina Macular Dystrophy: Phenotypic Variability and Computational Analysis of Disease-Associated Noncoding VariantsDavid J Green, Eva Lenassi, Cerys S Manning, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 17, 2020
Establishing Genotype-phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and RehabilitationLeslie P Molina-Ramírez, Eva Lenassi, Jamie M Ellingford, et al.
Ophthalmology|November 9, 2013
Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutationEva Lenassi, Zubin Saihan, Valentina Cipriani, et al.
Orphanet Journal of Rare Diseases|August 9, 2013
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencingHeather B Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
The American Journal of Pathology|June 11, 2013
Complement component C3 plays a critical role in protecting the aging retina in a murine model of age-related macular degenerationJaimie Hoh Kam, Eva Lenassi, Talat H Malik, et al.
Journal of Neurology|December 12, 2024
A rare cause of autosomal recessive ataxia with very late diagnosis and prolonged disease courseShakya Bhattacharjee, Eva Lenassi, Robert W Taylor, et al.
JAMA Ophthalmology|December 19, 2014
Clinical heterogeneity in a family with mutations in USH2AEva Lenassi, Anthony G Robson, Linda M Luxon, et al.
American Journal of Ophthalmology|October 6, 2012
Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1)Eva Lenassi, Eric Troeger, Robert Wilke, 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.
Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Investigative Ophthalmology & Visual Science|June 14, 2021
North Carolina Macular Dystrophy: Phenotypic Variability and Computational Analysis of Disease-Associated Noncoding VariantsDavid J Green, Eva Lenassi, Cerys S Manning, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 17, 2020
Establishing Genotype-phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and RehabilitationLeslie P Molina-Ramírez, Eva Lenassi, Jamie M Ellingford, et al.
Ophthalmology|November 9, 2013
Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutationEva Lenassi, Zubin Saihan, Valentina Cipriani, et al.
Orphanet Journal of Rare Diseases|August 9, 2013
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencingHeather B Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi, et al.
Pageof 3