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Eyvind Rødahl's picture

Eyvind Rødahl

Professor
Department of Clinical Medicine
  • E-mailEyvind.Rodahl@uib.no
  • Visitor Address
    Department of Ophthalmology, Haukeland University Hospital
  • Postal Address
    Postboks 7804
    5020 Bergen
Selected publications
  • Christensen, Anne Elisabeth; Bruland, Ove; Vedeler, Anni; Saraste, Jaakko; Schönheit, Jürgen; Bredrup, Cecilie; Knappskog, Per; Rødahl, Eyvind. 2015. Development of congenital stromal corneal dystrophy is dependent on export and extracellular deposition of truncated decorin. Investigative Ophthalmology and Visual Science. 56: 2909-2915. doi: 10.1167/iovs.14-16014
  • Bredrup, Cecilie; Johansson, Stefan; Bindoff, Laurence; Sztromwasser, Pawel Szymon; Kråkenes, Jostein; Christensen, Anne Elisabeth; Brurås, Kari Røine; Lind, Ola; Boman, Helge; Knappskog, Per; Rødahl, Eyvind. 2015. High myopia-excavated optic disc anomaly associated with a frameshift mutation in the MYC-binding protein 2 gene (MYCBP2). American Journal of Ophthalmology. 159: 973-979. doi: 10.1016/j.ajo.2015.01.021
  • Ueland, Hans Olav; Uchermann, Aleksander; Rødahl, Eyvind. 2014. Levator recession with adjustable sutures for correction of upper eyelid retraction in thyroid eye disease. Acta Ophthalmologica. 92: 793-797. doi: 10.1111/aos.12404
  • Gulati, Shashi; Ueland, Hans Olav; Haugen, Olav H.; Danielsen, Arild; Rødahl, Eyvind. 2015. Long-term follow-up of patients with thyroid eye disease treated with endoscopic orbital decompression. Acta Ophthalmologica. 93: 178-183. doi: 10.1111/aos.12469
  • Rødahl, Eyvind; Knappskog, Per; Majewski, Jacek; Johansson, Stefan; Telstad, Wenche; Kråkenes, Jostein; Boman, Helge. 2013. Variants of anterior segment dysgenesis and cerebral involvement in a large family with a novel COL4A1 mutation. American Journal of Ophthalmology. 155: 946-953. doi: 10.1016/j.ajo.2012.11.028
  • Bredrup, Cecilie; Saunier, Sophie; Oud, Machteld M.; Fiskerstrand, Torunn; Hoischen, Alexander; Brackman, Damien; Leh, Sabine; Midtbø, Marit; Filhol, Emilie; Bole-Feysot, Christine; Nitschke, Patrick; Gilissen, Christian; Haugen, Olav H.; Sanders, Jan-Stephan F.; Stolte-Dijkstra, Irene; Mans, Dorus A.; Steenbergen, Eric J.; Hamel, Ben C.J.; Matignon, Marie; Pfundt, Rolph; Jeanpierre, Cécilie; Boman, Helge; Veltman, Joris A.; Rødahl, Eyvind; Knappskog, Per; Knoers, Nine V.A.M.; Roepman, Ronald; Arts, Heleen .H. 2011. Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. American Journal of Human Genetics. 89: 634-643. doi: 10.1016/j.ajhg.2011.10.001
Academic lecture
  • Show author(s) (1997). Pax 6 genet ved utviklingsanomalier i fremre avsnitt av øyet.
Abstract
  • Show author(s) (2010). Do neurologists acknowledge visual field defects in stroke patients? European Journal of Neurology. 64-64.
  • Show author(s) (2008). Visual impairment in children in Norway. Acta Ophthalmologica. 53-53.

More information in national current research information system (CRIStin)

Fields of competence 
Eye
Hereditary eye disorders
Orbit
Thyroid eye disease