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- 2023
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Mark
A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing
(
- Contribution to journal › Article
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Mark
Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis
(
- Contribution to journal › Article
- 2022
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Mark
Dexamethasone eye-drops for treatment of retinopathy of prematurity
(
- Contribution to journal › Article
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Mark
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy
(
- Contribution to journal › Article
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Mark
Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration : A Systematic Review with Meta-Analyses
(
- Contribution to journal › Scientific review
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Mark
A novel phenotype associated with the R162W variant in the KCNJ13 gene
(
- Contribution to journal › Article
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Mark
A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes
(
- Contribution to journal › Article
- 2021
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Mark
Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene
(
- Contribution to journal › Article
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Mark
Full-field electroretinography in age-related macular degeneration : an overall retinal response
(
- Contribution to journal › Article
- 2020
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Mark
Clinical phenotype and course of PDE6A-associated retinitis pigmentosa disease, characterized in preparation for a gene supplementation trial
(
- Contribution to journal › Article
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Mark
Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Longitudinal changes of macular curvature in patients with retinitis pigmentosa
(
- Contribution to journal › Article
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Mark
Long-term effects of hyperbaric oxygen therapy on visual acuity and retinopathy
(
- Contribution to journal › Article
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Mark
Full-field Electroretinography in Age-related Macular Degeneration : can retinal electrophysiology predict the subjective visual outcome of cataract surgery?
(
- Contribution to journal › Article
- 2019
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Mark
Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
(
- Contribution to journal › Letter
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Mark
A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa
(
- Contribution to journal › Article
- 2018
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Mark
Presence of chronic diabetic foot ulcers is associated with more frequent and more advanced retinopathy
(
- Contribution to journal › Article
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Mark
Cerebral Functional Magnetic Resonance Imaging and Multifocal Visual Evoked Potentials in a Patient with Unexplained Impairment of Visual Function : A Case Report
(
- Contribution to journal › Article
- 2017
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Mark
Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome
(
- Contribution to journal › Article
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Mark
The clinical phenotype of CNGA3-related achromatopsia : Pretreatment characterization in preparation of a gene replacement therapy trial
(
- Contribution to journal › Article
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Mark
Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC
(
- Contribution to journal › Article
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Mark
An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS
(
- Contribution to journal › Article
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Mark
Reduction of rod and cone function in 6.5-year-old children born extremely preterm
(
- Contribution to journal › Article
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Mark
Ataxia-pancytopenia syndrome with SAMD9L mutations
(
- Contribution to journal › Article
- 2016
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Mark
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
(
- Contribution to journal › Article
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Mark
A cross-linked hyaluronic acid hydrogel (Healaflow(®)) as a novel vitreous substitute.
2016) In Graefe's Archive for Clinical and Experimental Ophthalmology(
- Contribution to journal › Article
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Mark
Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy.
2016) In Ophthalmology(
- Contribution to journal › Article
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Mark
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility
(
- 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
(
- Contribution to journal › Article
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Mark
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
(
- Contribution to journal › Article
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Mark
Macular function in preterm children at school age
(
- Contribution to journal › Article
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Mark
Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function
(
- Contribution to journal › Article
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Mark
Fixation stability and implication for multifocal electroretinography in patients with neovascular age-related macular degeneration after anti-VEGF treatment
(
- Contribution to journal › Article
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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
- 2015
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Mark
Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy.
2015) In Graefe's Archive for Clinical and Experimental Ophthalmology(
- Contribution to journal › Article
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Mark
Macular function measured by binocular mfERG and compared with macular structure in healthy children.
(
- Contribution to journal › Article
- 2014
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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.
(
- Contribution to journal › Article
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Mark
Cone implicit time as a predictor of visual outcome in macular hole surgery.
(
- Contribution to journal › Article
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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
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Mark
Alteration of Vitreal Retinoschisin Level in Human Primary Retinal Detachment.
(
- Contribution to journal › Letter
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Mark
Genotype-phenotype Correlations, and Retinal Function and Structure in von Hippel-Lindau Disease.
(
- Contribution to journal › Article
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Mark
Photoreceptor Function in School-Aged Children is Affected by Preterm Birth.
(
- Contribution to journal › Article
- 2013
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Mark
Vitreous levels of oxidative stress biomarkers and the radical-scavenger α(1)-microglobulin/A1M in human rhegmatogenous retinal detachment.
(
- Contribution to journal › Article
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Mark
Angiography and mfERG show that blood supply to the pig retina may be both ipsilateral and contralateral.
(
- Contribution to journal › Article
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Mark
Intravitreal Injection of Triamcinolone Acetonide into Healthy Rabbit Eyes Alters Retinal Function and Morphology
(
- Contribution to journal › Article
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Mark
Macular dysfunction in drusen maculopathy assessed with multifocal electroretinogram and optical coherence tomography.
(
- Contribution to journal › Article
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Mark
Transcutaneous Oximetry but not Arterial Toe Blood Pressure or Ankle-Brachial Index is related to Macular Thickness in Patients with Chronic Diabetic Foot Ulcers
(
- Contribution to journal › Article
- 2012
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Mark
Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease
(
- Contribution to journal › Article
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Mark
Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy.
(
- Contribution to journal › Article
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Mark
Retinal function and morphology in rabbit after intravitreal injection of VEGF inhibitors.
(
- Contribution to journal › Article
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Mark
Clinical and electrophysiologic outcome in patients with neovascular glaucoma treated with and without bevacizumab.
(
- Contribution to journal › Article
- 2011
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Mark
Experimental vitreous tamponade using polyalkylimide hydrogel
(
- Contribution to journal › Article
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Mark
Endovascular Coiling of the Ophthalmic Artery in Pigs to Induce Retinal Ischemia
(
- Contribution to journal › Article
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Mark
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia
(
- Contribution to journal › Article
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Mark
Evaluation of viscoelastic poly(ethylene glycol) sols as vitreous substitutes in an experimental vitrectomy model in rabbits
(
- 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
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
Alteration of rod and cone function in children with Usher syndrome.
(
- Contribution to journal › Article
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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
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
(
- Contribution to journal › Article
- 2010
-
Mark
Identification of Retinal Autoantigens in a Young Patient with Osteosarcoma and a Paraneoplastic Retinitis
2010) 39th Annual Meeting of the Scandinavian-Society-for-Immunology/Baltic-Immunological-Society Meeting In Scandinavian Journal of Immunology 71(6). p.479-479(
- Contribution to journal › Published meeting abstract
-
Mark
Evaluation of Macular Structure and Function by OCT and Electrophysiology in Patients with Vitelliform Macular Dystrophy Due to Mutations in BEST1
(
- Contribution to journal › Article
-
Mark
Electrophysiological Assessment of Retinal Function During 6 Months of Bevacizumab Treatment in Neovascular Age-Related Macular Degeneration
(
- Contribution to journal › Article
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Mark
Treatments for all RP-patients?
(
- Contribution to journal › Published meeting abstract
-
Mark
Macular disorder in defined genotype in inherent retinal degeneration measured by OCT and mfERG
(
- Contribution to journal › Published meeting abstract
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Mark
Transcutaneous Oximetry But Not Arterial Toe Blood Pressure Predicts Macular Thickness In Patients With Chronic Diabetic Foot Ulcers
(
- Contribution to journal › Published meeting abstract
-
Mark
Improved retinal function after trabeculectomy in glaucoma patients.
(
- Contribution to journal › Article
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Mark
Long-term 12 year follow-up of X-linked congenital retinoschisis.
(
- 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
Multifocal electroretinogram for functional evaluation of retinal injury following ischemia-reperfusion in pigs.
(
- Contribution to journal › Article
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Mark
RECOVERY OF RETINAL FUNCTION AFTER RECENT-ONSET RHEGMATOGENOUS RETINAL DETACHMENT IN RELATION TO TYPE OF SURGERY.
(
- Contribution to journal › Article
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Mark
Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open-angle glaucoma and neovascular glaucoma.
(
- Contribution to journal › Article
- 2009
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Mark
Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)
(
- Contribution to journal › Article
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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.
(
- Contribution to journal › Article
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Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
(
- Contribution to journal › Article
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Mark
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene
(
- Contribution to journal › Article
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Mark
The porcine retinal vasculature can be accessed using an endovascular approach, a new experimental model for retinal ischemia.
(
- Contribution to journal › Article
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Mark
Rifabutin accumulates in the lens and reduces retinal function in the rabbit eye
(
- Contribution to journal › Article
- 2008
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Mark
Retinal Function after Vitrectomy
(
- Contribution to journal › Article
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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
Autosomal dominant inheritance in pericentral retinal dystrophy, an atypical form of retinitis pigmentosa (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
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Mark
Autoantibodies against bestrophin in a patient with vitelliform paraneoplastic retinopathy and a metastatic choroidal malignant melanoma.
(
- Contribution to journal › Article
- 2007
-
Mark
Retinal function after scleral buckling for recent onset rhegmatogenous retinal detachment: assessment with electroretinography and optical coherence tomography.
(
- Contribution to journal › Article
-
Mark
Retinal function and PKC alpha expression after focal laser photocoagulation.
(
- Contribution to journal › Article
- 2006
-
Mark
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration
(
- Contribution to journal › Article
-
Mark
Developments in molecular genetics and electrophysiology in inherited retinal disorders.
(
- Contribution to journal › Scientific review
-
Mark
Retinal function in rabbits does not improve 4-5 months after terminating treatment with vigabatrin.
(
- Contribution to journal › Article
-
Mark
Retinal function and histopathology in rabbits treated with Topiramate.
(
- Contribution to journal › Article
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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
-
Mark
Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2.
(
- Contribution to journal › Article
-
Mark
Multifocal electroretinography and fluorescein angiography in retinal vein occlusion.
(
- Contribution to journal › Article
- 2005
-
Mark
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
(
- Contribution to journal › Article
-
Mark
Multifocal visual evoked potentials-a method study of responses from small sectors of the visual field.
(
- Contribution to journal › Article
-
Mark
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
(
- Contribution to journal › Article
-
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
-
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
Reduced full-field electroretinogram (ERG) in a patient treated with methotrexate.
(
- Contribution to journal › Article
-
Mark
Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy.
(
- Contribution to journal › Article
-
Mark
Standardized full-field electroretinography in rabbits.
(
- 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
Multifocal electroretinogram in branch retinal vein occlusion.
(
- Contribution to journal › Article
-
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
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
-
Mark
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy
(
- Contribution to journal › Article
-
Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
(
- Contribution to journal › Article
-
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
- 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
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS
(
- Contribution to journal › Article
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Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
(
- 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
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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
Gör balansprov på alla döva småbarn! : Tidig upptäckt av Ushers syndrom ökar möjligheterna till kommunikation vid senare dövblindhet
(
- Contribution to journal › Article
- 1997
-
Mark
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region, but splice defects in two families
(
- 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
-
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
- 1995
-
Mark
Phenotype variation within a choroideremia family lacking the entire CHM gene
(
- Contribution to journal › Article
- 1992
-
Mark
A six generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135–leucine)
(
- Contribution to journal › Article