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- 2016
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Mark
Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
(
- Contribution to journal › Article
- 2014
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Mark
Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab.
(
- Contribution to journal › Article
-
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.
(
- Contribution to journal › Article
- 2013
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Mark
Intravitreal Injection of Triamcinolone Acetonide into Healthy Rabbit Eyes Alters Retinal Function and Morphology
(
- Contribution to journal › Article
- 2012
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Mark
Retinal function and morphology in rabbit after intravitreal injection of VEGF inhibitors.
(
- Contribution to journal › Article
- 2011
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Mark
Electrophysiological studies in newly onset type 2 diabetes without visible vascular retinopathy.
(
- Contribution to journal › Article
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Mark
Alteration of rod and cone function in children with Usher syndrome.
(
- Contribution to journal › Article
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Mark
Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy.
(
- Contribution to journal › Article
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Mark
Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
(
- Contribution to journal › Article
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Mark
Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome.
(
- Contribution to journal › Article
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Mark
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
(
- Contribution to journal › Article
- 2010
-
Mark
Using multifocal electroretinography hard exudates affect macular function in eyes with diabetic retinopathy
(
- Contribution to journal › Article
-
Mark
Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open-angle glaucoma and neovascular glaucoma.
(
- Contribution to journal › Article
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Mark
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
(
- Contribution to journal › Article
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Mark
Long-term 12 year follow-up of X-linked congenital retinoschisis.
(
- Contribution to journal › Article
-
Mark
Improved retinal function after trabeculectomy in glaucoma patients.
(
- Contribution to journal › Article
- 2009
-
Mark
Dose-related changes in retinal function and PKC-alpha expression in rabbits on vigabatrin medication : Effect of vigabatrin in the rabbit eye.
(
- Contribution to journal › Article
-
Mark
Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)
(
- Contribution to journal › Article
-
Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
(
- Contribution to journal › Article
-
Mark
Thyroid-Associated Ophthalmopathy after Treatment for Graves' Hyperthyroidism with Antithyroid Drugs or Iodine-131.
(
- Contribution to journal › Article
-
Mark
Rifabutin accumulates in the lens and reduces retinal function in the rabbit eye
(
- Contribution to journal › Article
- 2008
-
Mark
Multifocal electroretinogram (mfERG) in patients with diabetes mellitus and an enlarged foveal avascular zone (FAZ)
(
- Contribution to journal › Article
-
Mark
Full-field electroretinography in young patients with Usher syndrome ( Abstracts of the XXXVIII Nordic Congress of Ophthalmology 14-17 June 2008)
(
- Contribution to journal › Published meeting abstract
-
Mark
Full-field electroretinography and marked variability in clinical phenotype of Alström syndrome.
(
- Contribution to journal › Article
-
Mark
Full-field ERG and visual fields in patients 5 years after discontinuing vigabatrin therapy.
(
- Contribution to journal › Article
- 2006
-
Mark
Retinal function and histopathology in rabbits treated with Topiramate.
(
- Contribution to journal › Article
-
Mark
Retinal function in rabbits does not improve 4-5 months after terminating treatment with vigabatrin.
(
- Contribution to journal › Article
-
Mark
Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2.
(
- Contribution to journal › Article
- 2005
-
Mark
Multifocal electroretinography (mfERG) in insulin dependent diabetics with and without clinically apparent retinopathy
(
- Contribution to journal › Article
-
Mark
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
(
- Contribution to journal › Article
- 2004
-
Mark
Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin
(
- Contribution to journal › Article
-
Mark
Macular function assessed with mfERG before and after panretinal photocoagulation in patients with proliferative diabetic retinopathy.
(
- Contribution to journal › Article
-
Mark
Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.
(
- Contribution to journal › Article
-
Mark
Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy.
(
- Contribution to journal › Article
-
Mark
Reduced full-field electroretinogram (ERG) in a patient treated with methotrexate.
(
- Contribution to journal › Article
- 2003
-
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
-
Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
(
- Contribution to journal › Article
- 2001
-
Mark
Electrophysiologic findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene
(
- Contribution to journal › Article
- 1999
-
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
-
Mark
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS
(
- Contribution to journal › Article
-
Mark
Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system
(
- Contribution to journal › Article
-
Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
(
- Contribution to journal › Article
-
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
- 1997
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
(
- Contribution to journal › Article
-
Mark
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
(
- Contribution to journal › Article
-
Mark
Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
(
- Contribution to journal › Article
- 1995
-
Mark
Phenotype variation within a choroideremia family lacking the entire CHM gene
(
- Contribution to journal › Article