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- 2004
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Mark
Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy.
(
- Contribution to journal › Article
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Mark
Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.
(
- Contribution to journal › Article
- 2003
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Mark
Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes
(
- Contribution to journal › Article
-
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
-
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
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Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
(
- Contribution to journal › Article
- 2001
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Mark
Electrophysiologic findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene
(
- Contribution to journal › Article
- 1999
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Mark
Digenic inheritance of a ROM1 gene mutation with a peripherin/RDS or rhodopsin mutation in families with retinitis pigmentosa
(
- Contribution to journal › Article
- 1998
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Mark
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration
(
- Contribution to journal › Article
-
Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
(
- Contribution to journal › Article