Sten Andréasson
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- 2003
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Mark
Multifocal electroretinogram in branch retinal vein occlusion.
(
- Contribution to journal › Article
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Mark
Mutation screening of patients with Leber congenital amaurosis or the enhanced S-cone syndrome reveals a lack of sequence variations in the NRL gene
(
- Contribution to journal › Article
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Mark
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene
(
- Contribution to journal › Article
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Mark
Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).
(
- Contribution to journal › Article
- 2002
-
Mark
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy
(
- Contribution to journal › Article
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Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
(
- Contribution to journal › Article
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Mark
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene
(
- Contribution to journal › Article
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Mark
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases
(
- Contribution to journal › Article
- 2001
-
Mark
Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)
(
- Contribution to journal › Article
-
Mark
Electrophysiologic findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene
(
- Contribution to journal › Article