Clinical research in families with inherited retinal degeneration
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- 2022
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Mark
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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Mark
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
- 2021
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Mark
Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene
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- Contribution to journal › Article
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Mark
Association of Docosahexaenoic Acid and Arachidonic Acid Serum Levels with Retinopathy of Prematurity in Preterm Infants
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- Contribution to journal › Article
- 2020
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Mark
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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Mark
A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa
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- Contribution to journal › Article
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Mark
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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Mark
Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
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- Contribution to journal › Letter
- 2018
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Mark
Electrophysiology - when nothing is seen
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- Thesis › Doctoral thesis (compilation)
- 2017
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Mark
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