Clinical research in families with inherited retinal degeneration
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- 2024
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Ophthalmological outcome of 6.5 years children treated for retinopathy of prematurity : A Swedish register study
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- Contribution to journal › Article
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Treatment for retinopathy of prematurity in Sweden 2008–2021 : Reduced gestational age of treated infants and remaining differences in treatment type and recurrence rates between hospitals
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- Contribution to journal › Article
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Ophthalmic manifestations in children with tuberous sclerosis complex
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- Contribution to journal › Article
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The impact of COVID-19 on aflibercept treatment of neovascular AMD in Sweden – data from the Swedish Macula Register
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- Contribution to journal › Article
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The prevalence of visual axis opacification in the Swedish Pediatric Cataract Register
2024) In Acta Ophthalmologica(
- Contribution to journal › Article
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Maculopathy and adult-onset ataxia in patients with biallelic MFSD8 variants
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- Contribution to journal › Article
- 2023
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Validation of DIGIROP models and decision support tool for prediction of treatment for retinopathy of prematurity on a contemporary Swedish cohort
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- Contribution to journal › Article
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Co-occurrence of CLCN2-related leukoencephalopathy and SPG56
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- Contribution to journal › Article
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Case report : Bilateral damage to the immature optic radiation and secondary massive loss of retinal ganglion cells causing tunnel vision
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- Contribution to journal › Article
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Prognostic Value of Parenteral Nutrition Duration on Risk of Retinopathy of Prematurity : Development and Validation of the Revised DIGIROP Clinical Decision Support Tool
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- Contribution to journal › Article
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Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
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- Contribution to journal › Article
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Visual outcome at 2.5 years of age in ω-3 and ω-6 long-chain polyunsaturated fatty acid supplemented preterm infants : a follow-up of a randomized controlled trial
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- Contribution to journal › Article
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A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing
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- Contribution to journal › Article
- 2022
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Low fraction of fetal haemoglobin is associated with retinopathy of prematurity in the very preterm infant
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- Contribution to journal › Article
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Abnormal Appearance of the Area Centralis in Labrador Retrievers With an ABCA4 Loss-of-function Mutation
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- Contribution to journal › Article
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Electrophysiological evaluation and 18-month follow-up of two regimens with aflibercept for neovascular age-related macular degeneration
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- Contribution to journal › Article
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A novel phenotype associated with the R162W variant in the KCNJ13 gene
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- Contribution to journal › Article
- 2021
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Association of Docosahexaenoic Acid and Arachidonic Acid Serum Levels with Retinopathy of Prematurity in Preterm Infants
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- Contribution to journal › Article
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Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene
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- Contribution to journal › Article
- 2020
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New modifications of Swedish ROP guidelines based on 10-year data from the SWEDROP register
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- Contribution to journal › Article
- 2019
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Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
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- Contribution to journal › Letter
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Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene
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- Contribution to journal › Article
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A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa
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- Contribution to journal › Article
- 2018
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Electrophysiology - when nothing is seen
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- Thesis › Doctoral thesis (compilation)
- 2017
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The clinical phenotype of CNGA3-related achromatopsia : Pretreatment characterization in preparation of a gene replacement therapy trial
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- Contribution to journal › Article
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Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome
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- Contribution to journal › Article
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Central retinal vein occlusion in younger Swedish adults : Case reports and review of the literature
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- Contribution to journal › Article
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Ataxia-pancytopenia syndrome with SAMD9L mutations
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- Contribution to journal › Article
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Reduction of rod and cone function in 6.5-year-old children born extremely preterm
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- Contribution to journal › Article
- 2009
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Rifabutin accumulates in the lens and reduces retinal function in the rabbit eye
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- Contribution to journal › Article
- 2004
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Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin
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- Contribution to journal › Article