J. Fuchs

发表

Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease.

H. Fledelius, T. Rosenberg, D. Schorderet, 2011, American journal of human genetics.

Visual outcomes in relation to time to treatment in neovascular age‐related macular degeneration

M. Larsen, H. Lund‐Andersen, B. Sander, 2015, Acta ophthalmologica.

Safety study of 38 503 intravitreal ranibizumab injections performed mainly by physicians in training and nurses in a hospital setting

M. Larsen, H. Lund‐Andersen, P. Hasler, 2015, Acta ophthalmologica.

Neovascular age‐related macular degeneration treated with ranibizumab or aflibercept in the same large clinical setting: visual outcome and number of injections

M. Larsen, H. Lund‐Andersen, B. Sander, 2017, Acta ophthalmologica.

Retinitis pigmentosa associated with a mutation in BEST1

R. Iezzi, L. Dalvin, J. Chiang, 2016, American journal of ophthalmology case reports.

Morphological features in eyes with endophthalmitis after cataract surgery – histopathology and optical coherence tomography assessment

J. Prause, J. Kiilgaard, M. la Cour, 2016, Acta ophthalmologica.

Predictors of 1‐year visual outcome in neovascular age‐related macular degeneration following intravitreal ranibizumab treatment

M. Larsen, H. Lund‐Andersen, B. Sander, 2013, Acta ophthalmologica.

Automated artificial intelligence‐based system for clinical follow‐up of patients with age‐related macular degeneration

B. Thiesson, S. Hamann, I. Potapenko, 2022, Acta ophthalmologica.

Intravitreal Injections with Vascular Endothelial Growth Factor Inhibitors: A Practical Approach

Chantal Dysli, R. Mastropasqua, L. J. Cehofski, 2020, Ophthalmology and Therapy.

TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

Flemming Skovby, Christian Hagemeier, P. Robinson, 2002, Human mutation.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

Flemming Skovby, Christian Hagemeier, P. Robinson, 2001, European Journal of Human Genetics.

The disease burden of congenital toxoplasmosis in Denmark, 2014

K. Burgdorf, C. R. Stensvold, H. Nielsen, 2017, PLoS ONE.

Detection of oedema on optical coherence tomography images using deep learning model trained on noisy clinical data

B. Thiesson, S. Hamann, I. Potapenko, 2021, Acta ophthalmologica.

Glaucoma prevalence in the Nordic countries

E. Goldschmidt, J. Fuchs, Christina Raitta, 1989, Acta ophthalmologica.

Vogt–Koyanagi–Harada syndrome in Greenland

D. Milea, M. la Cour, J. Fuchs, 2008, Acta ophthalmologica.

Refraction in diabetics during metabolic dysregulation, acute or chronic

H. Fledelius, J. Fuchs, A. Reck, 1990, Acta ophthalmologica.

Hereditary High Hypermetropia in the Faroe Islands

H. Fledelius, T. Rosenberg, E. Scherfig, 2005, Ophthalmic genetics.

Retinal detachment after cataract extraction in myopic eyes

T. Olsen, K. Bjerrum, V. Henning, 1998, Journal of cataract and refractive surgery.

Neovascular age-related macular degeneration: is it worthwhile treating an eye with poor visual acuity, if the visual acuity of the fellow eye is good?

M. Larsen, H. Lund‐Andersen, B. Sander, 2017, Eye.

A 4-year longitudinal study of 555 patients treated with ranibizumab for neovascular age-related macular degeneration.

M. Larsen, H. Lund‐Andersen, B. Sander, 2013, Ophthalmology.

Glaucoma blindness in Denmark

E. Goldschmidt, J. Fuchs, K. Nissen, 1992, Acta ophthalmologica.

Retinal detachment after cataract

T. Olsen, K. Bjerrum, V. Henning, 1998 .