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Acta Ophthalmologica
|
July 20, 2010
Heritability of optic disc diameters: a twin study
Dragana Drobnjak, Nina C B B Taarnhøj, Paul Mitchell, et al.
Acta Ophthalmologica
|
April 12, 2025
Efficacy of interventions for myopia control in children: A systematic review with network meta-analyses
Diana Chabané Schmidt, Anders Hvid-Hansen, Nina Jacobsen, et al.
Ophthalmic Genetics
|
April 5, 2021
Oliver McFarlane syndrome: two new cases and a review of the literature
Kristian Lisbjerg, Mette K G Andersen, Mette Bertelsen, et al.
Clinical Genetics
|
June 27, 2026
Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy
Katrine M Johannesen, Karen Grønskov, Line Kessel, et al.
Ophthalmology Science
|
March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene Neparvovec
M Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Journal of Personalized Medicine
|
October 25, 2024
Evaluating the Feasibility of a Telescreening Program for Retinopathy of Prematurity (ROP) in Denmark
Hajer A Al-Abaiji, Regitze Bangsgaard, Mads Kofod, et al.
Human Molecular Genetics
|
October 29, 2024
A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment
Menachem V K Sarusie, Cecilia Rönnbäck, Cathrine Jespersgaard, et al.
Diabetes Care
|
November 12, 2020
Identification and Characterization of Patients With Rapid Progression of Diabetic Retinopathy in the Danish National Screening Program
Jakob Grauslund, Anne S Thykjær, Ryo Kawasaki, et al.
European Journal of Human Genetics : EJHG
|
March 11, 2026
Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR
Muhammad Farooq, Gitte Hoffmann Bruun, Menachem V K Sarusie, et al.
Human Mutation
|
May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
Julia Felden, Britta Baumann, Manir Ali, et al.
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of 18
Search research articles
Search
Showing results (161-170 of 173) with videos related to
Sort By:
Page
of 18
Acta Ophthalmologica
|
July 20, 2010
Heritability of optic disc diameters: a twin study
Dragana Drobnjak, Nina C B B Taarnhøj, Paul Mitchell, et al.
Acta Ophthalmologica
|
April 12, 2025
Efficacy of interventions for myopia control in children: A systematic review with network meta-analyses
Diana Chabané Schmidt, Anders Hvid-Hansen, Nina Jacobsen, et al.
Ophthalmic Genetics
|
April 5, 2021
Oliver McFarlane syndrome: two new cases and a review of the literature
Kristian Lisbjerg, Mette K G Andersen, Mette Bertelsen, et al.
Clinical Genetics
|
June 27, 2026
Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy
Katrine M Johannesen, Karen Grønskov, Line Kessel, et al.
Ophthalmology Science
|
March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene Neparvovec
M Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Journal of Personalized Medicine
|
October 25, 2024
Evaluating the Feasibility of a Telescreening Program for Retinopathy of Prematurity (ROP) in Denmark
Hajer A Al-Abaiji, Regitze Bangsgaard, Mads Kofod, et al.
Human Molecular Genetics
|
October 29, 2024
A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment
Menachem V K Sarusie, Cecilia Rönnbäck, Cathrine Jespersgaard, et al.
Diabetes Care
|
November 12, 2020
Identification and Characterization of Patients With Rapid Progression of Diabetic Retinopathy in the Danish National Screening Program
Jakob Grauslund, Anne S Thykjær, Ryo Kawasaki, et al.
European Journal of Human Genetics : EJHG
|
March 11, 2026
Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR
Muhammad Farooq, Gitte Hoffmann Bruun, Menachem V K Sarusie, et al.
Human Mutation
|
May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
Julia Felden, Britta Baumann, Manir Ali, et al.
Page
of 18