Search Results - "Andersen, Mette K. G."

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  1. 1

    Integrity of the cone photoreceptor mosaic in oligocone trichromacy by Michaelides, Michel, Rha, Jungtae, Dees, Elise W, Baraas, Rigmor C, Wagner-Schuman, Melissa L, Mollon, John D, Dubis, Adam M, Andersen, Mette K G, Rosenberg, Thomas, Larsen, Michael, Moore, Anthony T, Carroll, Joseph

    “…Oligocone trichromacy (OT) is an unusual cone dysfunction syndrome characterized by reduced visual acuity, mild photophobia, reduced amplitude of the cone…”
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    Journal Article
  2. 2

    Phenotypic characteristics of Danish patients with achromatopsia by Andersen, Mette K. G., Bertelsen, Mette, Gundestrup, Svend, Grønskov, Karen, Kessel, Line

    Published in Acta ophthalmologica (Oxford, England) (01-09-2024)
    “…Purpose To describe the phenotype of Danish patients with genetically verified achromatopsia (ACHM) with special focus on signs of progression on structural or…”
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    Journal Article
  3. 3

    Oliver McFarlane syndrome: two new cases and a review of the literature by Lisbjerg, Kristian, Andersen, Mette K G, Bertelsen, Mette, Brost, Agnes G, Buchvald, Frederik F, Jensen, Rikke B, Bisgaard, Anne-Marie, Rosenberg, Thomas, Tümer, Zeynep, Kessel, Line

    Published in Ophthalmic genetics (01-08-2021)
    “…Oliver McFarlane syndrome is a rare syndrome. Clinical presentations include trichomegaly, chorioretinal degeneration, pituitary hormone deficits, and…”
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    Journal Article
  4. 4

    Oligocone trichromacy: clinical and molecular genetic investigations by Andersen, Mette K G, Christoffersen, Nynne L B, Sander, Birgit, Edmund, Carsten, Larsen, Michael, Grau, Tanja, Wissinger, Bernd, Kohl, Susanne, Rosenberg, Thomas

    “…To describe the phenotype and genotype of patients with a diagnosis of oligocone trichromacy (OT). Six unrelated patients had a detailed ophthalmic examination…”
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    Journal Article
  5. 5

    Oliver McFarlane syndrome: two new cases and a review of the literature by Lisbjerg, Kristian, Andersen, Mette K. G., Bertelsen, Mette, Brost, Agnes G., Buchvald, Frederik F., Jensen, Rikke B., Bisgaard, Anne-Marie, Rosenberg, Thomas, Tümer, Zeynep, Kessel, Line

    Published in Ophthalmic Genetics (04-07-2021)
    “…Oliver McFarlane syndrome is a rare syndrome. Clinical presentations include trichomegaly, chorioretinal degeneration, pituitary hormone deficits, and…”
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