Sten Andréasson
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- 2006
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Mark
Developments in molecular genetics and electrophysiology in inherited retinal disorders.
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- Contribution to journal › Scientific review
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Mark
mfERG in normal and lesioned rabbit retina.
2006) Psalmernas väg In Graefe's Archive for Clinical and Experimental Ophthalmology 244(1). p.83-89(
- Contribution to journal › Article
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Mark
Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2.
(
- Contribution to journal › Article
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Mark
Multifocal electroretinography and fluorescein angiography in retinal vein occlusion.
(
- Contribution to journal › Article
- 2005
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Mark
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
(
- Contribution to journal › Article
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Mark
Multifocal visual evoked potentials-a method study of responses from small sectors of the visual field.
(
- Contribution to journal › Article
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Mark
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
(
- Contribution to journal › Article
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Mark
Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease.
(
- Contribution to journal › Article
- 2004
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Mark
Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin
(
- Contribution to journal › Article
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Mark
Macular function assessed with mfERG before and after panretinal photocoagulation in patients with proliferative diabetic retinopathy.
(
- Contribution to journal › Article