Ulrika Kjellström
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- 2017
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Mark
An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS
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- Contribution to journal › Article
- 2016
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Mark
Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
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- Contribution to journal › Article
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Mark
Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene
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- Contribution to journal › Article
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Mark
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
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- Contribution to journal › Article
- 2015
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Mark
Reduced macular function in ABCA4 carriers.
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- Contribution to journal › Article
- 2014
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Mark
Association between genotype and phenotype in families with mutations in the ABCA4 gene.
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- Contribution to journal › Article
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Mark
Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full-field electroretinography in patients exposed to vigabatrin medication.
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- Contribution to journal › Article
- 2011
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Mark
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
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- Contribution to journal › Article
- 2010
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Mark
Ocular function and morphology in humans and rabbits exposed to vigabatrin medication
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- Thesis › Doctoral thesis (compilation)
- 2009
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Mark
Dose-related changes in retinal function and PKC-alpha expression in rabbits on vigabatrin medication : Effect of vigabatrin in the rabbit eye.
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- Contribution to journal › Article