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Acta Ophthalmologica|September 21, 2022
Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delGAnna Majander, Eeva-Marja Sankila, Aura Falck, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 28, 2025
Visual pathway function in adults born preterm with very low birth weight: a two-country birth cohort studyAnna P M Jørgensen, Maarit Kulmala, Dordi Austeng, et al.
Acta Ophthalmologica|April 10, 2023
Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucomaPerttu J Liuska, Abdessallam Tadji, Pauliina Repo, et al.
Journal of Medical Genetics|May 19, 2021
WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndromeKun Hu, Malgorzata Zatyka, Dewi Astuti, et al.
American Journal of Ophthalmology|February 16, 2020
In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3Joni A Turunen, Annamari T Immonen, Reetta-Stiina Järvinen, et al.
Acta Ophthalmologica|October 22, 2024
A retrospective longitudinal study of 52 Finnish patients with X-linked retinoschisisMira A Järvinen, Rigmor C Baraas, Anna Majander, et al.
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
Acta Ophthalmologica|May 12, 2023
Visual function in adults born preterm with very low birth weight-A two-country birth cohort studyMaarit Kulmala, Anna Perregaard Munch Jørgensen, Kristina Anna Djupvik Aakvik, et al.
Developmental Medicine and Child Neurology|August 2, 2025
Motor outcomes and visual function in adults born preterm with very low birthweightSilje D Benum, Urd E Svennevig, Anna Fivelstad, et al.
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