HA
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Genetics of the Eye and Anterior Segment Dysgenesis | 2024 | 88 | 277 | ||||
European Glaucoma Society – A guide on surgical innovation for glaucoma | British journal of ophthalmology | 2023 | 65 | 0 | |||
Corticostéroïdes et glaucome | Revue médicale suisse | 2023 | 88 | 65 | |||
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases | Ophthalmology science | 2023 | 62 | 26 | |||
Intraocular pressure reduction after femtolaser assisted cataract surgery and its association with the use of ultrasound | Medicina | 2021 | 167 | 83 | |||
Vitamin D and glaucoma: a critical review of the literature | Journal of Ophthalmology | 2020 | 668 | 180 | |||
A novel recessive RPGRIP1 mutation causing leber congenital amaurosis | Klinische Monatsblätter für Augenheilkunde | 2016 | 264 | 0 | |||
Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families | Human Mutation | 2014 | 249 | 0 | |||
Association between rate of binocular visual field change and vision-related quality of life: novel finding or spurious association? | JAMA Ophthalmology | 2014 | 219 | 0 | |||
Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract | British Journal of Ophthalmology | 2014 | 338 | 0 | |||
Femtosecond-laser assisted cataract surgery: a review | Acta Ophthalmologica | 2014 | 230 | 0 | |||
Anterior uveitis and cataract after rubella vaccination: a case report of a 12-month-old girl | Pediatrics | 2013 | 269 | 0 | |||
ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm | Human Molecular Genetics | 2013 | 258 | 0 |