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Meeting Abstract (7)
Journal Articles (2)

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Investigative Ophthalmology & Visual Science (8)
Translational Vision Science & Technology (1)

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ARVO Annual Meeting Abstract (7)
Articles (1)
Retina (1)

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Eye Anatomy and Disorders (2)
Genetics (2)
Retina (2)
Biochemistry and Molecular Biology (1)
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mutation (2)
abca4 gene (1)
autosomal recessive inheritance (1)
cyclic gmp (1)
dog, domestic (1)
electroretinography (1)
family (1)
fovea centralis (1)
genes (1)
homozygote (1)

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ARVO Annual Meeting Abstract June 2024

Natural history study of PRPF31-mediated retinal dystrophy

Josephine Prener Holtan; Kathrine Eriksen; ulrika kjellstrom; Jon Roger Eidet; Morten C Moe; Jørn-Ove Schjølberg; Mirta Mittelstedt Leal de Sousa; Magnar Bjørås; Ragnheidur Bragadóttir

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3107.

Articles February 2022

Abnormal Appearance of the Area Centralis in Labrador Retrievers With an ABCA4 Loss-of-function Mutation

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Björn Ekesten; Suvi Mäkeläinen; Stuart Ellis; Ulrika Kjellström; Tomas F. Bergström
TAGS: abca4 gene, dog, domestic, fovea centralis, likelihood ratio, loss of function mutation, mutation, ophthalmoscopy
Trans. Vis. Sci. Tech.. 2022; 11(2):36. https://doi.org/10.1167/tvst.11.2.36

ARVO Annual Meeting Abstract June 2020

Fundus autofluorescence and foveal appearance in Labrador Retriever dogs with an ABCA4 loss-of-function mutation.

Bjorn Ekesten; Suvi Mäkeläinen; Ulrika Kjellstrom; Tomas F Bergström

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):665.

ARVO Annual Meeting Abstract June 2020

Electrophysiological and morphological evaluation during 18 months follow-up of two regimens using Aflibercept for neovascular age-related macular degeneration (nAMD).

Marion Schroeder; Ulrika Kjellstrom; Monica Karin Loevestam-Adrian

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2641.

Retina November 2016

Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene

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Ulrika Kjellström; Patricia Veiga-Crespo; Sten Andréasson; Per Ekström
TAGS: cyclic gmp, family, genes, homozygote, mutation, plasma, retinitis pigmentosa, autosomal recessive inheritance, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2016; 57(14):6048-6057. https://doi.org/10.1167/iovs.16-19861

ARVO Annual Meeting Abstract September 2016

Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy

Konstantinos Nikopoulos; Pietro Farinelli; Beryl Royer-Bertrand; Nicola Bedoni; Ulrika Kjellström; Sten Andreasson; Miltiadis K Tsilimbaris; Chrysanthi Tsika; Stella Blazaki; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12)

ARVO Annual Meeting Abstract June 2013

Visual Prognosis and Association Between Geno - and Phenotype in Families with ABCA4 Mutations

Ulrika Kjellstrom; Sten Andreasson

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1327.

ARVO Annual Meeting Abstract March 2012

Characterization Of Macular Function And Morphology In Two Swedish Families With Genetically Identified Autosomal Dominant Retinitis Pigmentosa Prpf31 And Rho135/gucy2d

Wissam A. Aboud, Sr.; Ulrika Kjellstrom; Sten Andreasson; Vesna Ponjavic

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4592.

ARVO Annual Meeting Abstract April 2011

Optical Coherence Tomography as a Promising Method in the Follow-up of Patients Exposed to Vigabatrin Medication

Ulrika Kjellstrom; Vesna Ponjavic; Sten Andreasson

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5633.

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Online ISSN: 2164-2591

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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