HA
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Azacitidine-induced remission enables allogeneic transplantation in TET2/BCOR-mutant relapsed extranodal natural killer/T-cell lymphoma : a case report | Haematologica |  | 2026 | 5 | 23 | ||
| Genetics of the Eye and Anterior Segment Dysgenesis | | 2024 | 118 | 412 | |||
| European Glaucoma Society – A guide on surgical innovation for glaucoma | British journal of ophthalmology |  | 2023 | 81 | 0 | ||
| Corticostéroïdes et glaucome | Revue médicale suisse | | 2023 | 115 | 485 | ||
| 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 | 94 | 53 | ||
| Intraocular pressure reduction after femtolaser assisted cataract surgery and its association with the use of ultrasound | Medicina | | 2021 | 199 | 121 | ||
| Vitamin D and glaucoma: a critical review of the literature | Journal of Ophthalmology | | 2020 | 776 | 462 | ||
| A novel recessive RPGRIP1 mutation causing leber congenital amaurosis | Klinische Monatsblätter für Augenheilkunde | | 2016 | 289 | 0 | ||
| Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families | Human Mutation | | 2014 | 283 | 0 | ||
| Association between rate of binocular visual field change and vision-related quality of life: novel finding or spurious association? | JAMA Ophthalmology | | 2014 | 235 | 0 | ||
| Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract | British Journal of Ophthalmology | | 2014 | 372 | 0 | ||
| Femtosecond-laser assisted cataract surgery: a review | Acta Ophthalmologica | | 2014 | 257 | 0 | ||
| Anterior uveitis and cataract after rubella vaccination: a case report of a 12-month-old girl | Pediatrics | | 2013 | 299 | 0 | ||
| ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm | Human Molecular Genetics | | 2013 | 285 | 0 |
