S. Andreasson

发表

Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration: A Systematic Review with Meta-Analyses

Y. Subhi, T. Sørensen, T. Forshaw, 2022, Ophthalmologica.

Full‐field electroretinography in age‐related macular degeneration: an overall retinal response

T. Kjaer, T. Sørensen, T. Forshaw, 2020, Acta ophthalmologica.

Full‐field Electroretinography in Age‐related Macular Degeneration: can retinal electrophysiology predict the subjective visual outcome of cataract surgery?

T. Kjaer, T. Sørensen, T. Forshaw, 2020, Acta ophthalmologica.

Vitreous levels of oxidative stress biomarkers and the radical-scavenger α1-microglobulin/A1M in human rhegmatogenous retinal detachment

K. Arnér, F. Ghosh, S. Andreasson, 2013, Graefe's Archive for Clinical and Experimental Ophthalmology.

Retinal function and PKC alpha expression after focal laser photocoagulation

F. Ghosh, M. Malmsjö, A. Wackenfors, 2007, Graefe's Archive for Clinical and Experimental Ophthalmology.

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

P. Sieving, S. Jacobson, R. Salati, 2022, Human mutation.

Phenotype variations within a choroideremia family lacking the entire CHM gene.

F. Cremers, H. Bokhoven, H. van Bokhoven, 1995, Ophthalmic genetics.

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.

P. Sieving, B. Ehinger, R. Ayyagari, 2000, Archives of ophthalmology.

Seasonal changes in diel activity of Cottus poecilopus and C. gobio (Pisces) at the Arctic Circle

S. Andreasson, 1973 .

Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome.

A. Wright, K. Tornqvist, R. Riise, 2009, Acta ophthalmologica Scandinavica.

Full-field electroretinograms in individuals with the Laurence-Mood-Bardet-Biedl syndrome.

K. Tornqvist, R. Riise, S. Andreasson, 2009, Acta ophthalmologica Scandinavica.

Intrafamilial variation of the phenotype in Bardet–Biedl syndrome

N. Tommerup, T. Rosenberg, A. Wright, 1997, The British journal of ophthalmology.

The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy

A. Cideciyan, S. Jacobson, B. Lorenz, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Retinal function and histopathology in rabbits treated with Topiramate

T. Eriksson, S. Kjellström, V. Ponjavic, 2006, Documenta Ophthalmologica.

Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene

E. Zrenner, A. Meindl, C. Pusch, 2002, Graefe's Archive for Clinical and Experimental Ophthalmology.

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene

U. Kjellström, S. Andreasson, Susanne Martell, 2020, Ophthalmic genetics.

Full-field electroretinograms in a family with Mohr-Tranebjaerg syndrome.

H. Lubs, L. Tranebjaerg, V. Ponjavic, 2009, Acta ophthalmologica Scandinavica.

Endovascular coiling of the ophthalmic artery in pigs to induce retinal ischemia.

Bodil Gesslein, M. Malmsjö, Håkan Morén, 2011, Investigative ophthalmology & visual science.

Ataxia-pancytopenia syndrome with SAMD9L mutations

C. Nilsson, L. Nilsson, J. Davidsson, 2017, Neurology: Genetics.

A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute

F. Ghosh, S. Crafoord, S. Andreasson, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.

M. Abrahamson, B. Ehinger, V. Ponjavic, 1997, Ophthalmic genetics.

Full-field electroretinograms in infants with hereditary tapetoretinal degeneration.

V. Ponjavic, S. Andreasson, 2009, Acta ophthalmologica Scandinavica. Supplement.

Full‐field electroretinograms in patients with central areolar choroidal dystrophy

B. Ehinger, V. Ponjavic, S. Andreasson, 1994, Acta ophthalmologica.

Electroretinographic studies of families with dominant retinitis pigmentosa

S. Andreasson, 1991, Acta ophthalmologica.

Electroretinographic diagnosis in families with X‐linked retinitis pigmentosa

B. Ehinger, S. Andreasson, 1990, Acta ophthalmologica.

Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family

G. Holmgren, O. Sandgren, T. Fagerheim, 2000, Ophthalmic genetics.

Juvenile X-Linked Retinoschisis with Normal Scotopic b-Wave in the Electroretinogram at an Early Stage of the Disease

M. Abrahamson, L. Eksandh, S. Andreasson, 2005, Ophthalmic genetics.

Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy

M. Larsen, D. Sharon, Patrik Schatz, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin

L. Gränse, S. Kjellström, V. Ponjavic, 2004, Documenta Ophthalmologica.

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

V. Ponjavic, U. Kjellström, S. Andreasson, 2014, Acta ophthalmologica.

A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration.

O. Sandgren, P. Nilsson-ehle, M. Abrahamson, 1998, Ophthalmic genetics.

A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes

U. Kjellström, S. Andreasson, 2022, Molecular vision.

Electroretinograms in patients with achromatopsia

K. Tornqvist, S. Andreasson, 1991, Acta ophthalmologica.

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis

A. Hoischen, C. Rivolta, P. Farinelli, 2022, Frontiers in Cell and Developmental Biology.

Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.

T. L. McGee, G. Fishman, D. Sharon, 2002, Investigative ophthalmology & visual science.

F. Ghosh, V. Ponjavic, U. Kjellström, 2009, Graefe's Archive for Clinical and Experimental Ophthalmology.

Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations

B. J. Klevering, C. Klaver, B. Lorenz, 2013, Human mutation.

A cross-linked hyaluronic acid hydrogel (Healaflow ®) as a potential vitreous substitute

F. Ghosh, S. Crafoord, S. Andreasson, 2014 .

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

P. Sieving, S. Jacobson, R. Salati, 2005, European Journal of Human Genetics.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

Evaluation of viscoelastic poly(ethylene glycol) sols as vitreous substitutes in an experimental vitrectomy model in rabbits.

Christopher D. Pritchard, R. Langer, K. Arnér, 2011, Acta biomaterialia.

RETINAL FUNCTION AFTER VITRECTOMY

F. Ghosh, S. Andreasson, Karin Gjörloff Wallentén, 2008, Retina.

RECOVERY OF RETINAL FUNCTION AFTER RECENT-ONSET RHEGMATOGENOUS RETINAL DETACHMENT IN RELATION TO TYPE OF SURGERY

Patrik Schatz, S. Andreasson, 2010, Retina.

Clinical electroretinography in the dog with ganzfeld stimulation: A practical method of examining rod and cone function

P. Gouras, K. Narfström, S. Andreasson, 2005, Documenta Ophthalmologica.

Standardized full-field electroretinography in rabbits

B. Ehinger, S. Andréasson, K. Gjörloff, 2004, Documenta Ophthalmologica.

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

C. Scharfe, A. Meindl, S. Feil, 2000, Nature Genetics.

Multifocal ERG and full-field ERG in patients on long-term vigabatrin medication

S. Andréasson, V. Ponjavic, S. Andreasson, 2004, Documenta Ophthalmologica.

mfERG in normal and lesioned rabbit retina

S. Andréasson, F. Ghosh, K. Gjörloff, 2005, Graefe's Archive for Clinical and Experimental Ophthalmology.

The mutation spectrum of the bestrophin protein – functional implications

C. Wadelius, O. Sandgren, T. Rosenberg, 1999, Human Genetics.

Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia.

E. Zrenner, T. Rosenberg, B. Jurklies, 2011, Human molecular genetics.

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

S. Bolz, B. Jurklies, J. Heckenlively, 2009, Proceedings of the National Academy of Sciences.

Developments in molecular genetics and electrophysiology in inherited retinal disorders.

S. Andreasson, 2006, Acta ophthalmologica Scandinavica.

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Subhadra Jalali, Anand Swaroop, S. Jacobson, 2006, American journal of human genetics.

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

S. Jacobson, T. Strom, T. Rosenberg, 2016, PloS one.

Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene

P. Munroe, H. Eiberg, P. Uvebrant, 2000, Ophthalmic genetics.

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial.

E. Zrenner, B. Wissinger, T. Strasser, 2017, Investigative ophthalmology & visual science.

Identification of the gene responsible for Best macular dystrophy

M. Metzker, C. Wadelius, C. Austin, 1998, Nature Genetics.

Macular function measured by binocular mfERG and compared with macular structure in healthy children

G. Holmström, E. Larsson, H. Åkerblom, 2015, Documenta Ophthalmologica.

Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene.

C. Wadelius, B. Ehinger, V. Ponjavic, 1999, Ophthalmic genetics.

Full‐field electroretinograms during general anesthesia in normal children compared to examination with topical anesthesia

B. Ehinger, K. Tornqvist, S. Andreasson, 1993, Acta ophthalmologica.

Genomic Organization of Human DLG4, the Gene Encoding Postsynaptic Density 95

P. Bryant, O. Sandgren, N. Udar, 1999, Journal of neurochemistry.

Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene

M. Votruba, L. Gränse, S. Andréasson, 2003, Ophthalmic genetics.

A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.

T. Rosenberg, S. Bhattacharya, H. Eiberg, 2002, Investigative ophthalmology & visual science.

Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy

M. Bondeson, V. Ponjavic, Elisabeth Wittström, 2011, Ophthalmic genetics.

Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.

G. Abecasis, A. Swaroop, D. Breuer, 2009, American journal of human genetics.

Reduction of Rod and Cone Function in 6.5-Year-Old Children Born Extremely Preterm

G. Holmström, E. Larsson, H. Åkerblom, 2017, JAMA ophthalmology.

Macular function in preterm children at school age

G. Holmström, H. Åkerblom, S. Andreasson, 2016, Documenta Ophthalmologica.

Photoreceptor Function in School-Aged Children is Affected by Preterm Birth.

G. Holmström, E. Larsson, H. Åkerblom, 2014, Translational vision science & technology.

Reduced full-field electroretinogram (ERG) in a patient treated with methotrexate.

L. Gränse, S. Andréasson, V. Ponjavic, 2004, Acta ophthalmologica Scandinavica.

Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility.

C. Klaver, C. Rivolta, P. Farinelli, 2016, Human molecular genetics.

Macular dysfunction in drusen maculopathy assessed with multifocal electroretinogram and optical coherence tomography

J. Ruiz-Moreno, M. Lövestam-Adrian, K. Holm, 2008, Clinical ophthalmology.

Most patients with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency develop pathological or subnormal retinal function

Y. Liu, A. Nordenström, G. Holmström, 2016, Acta paediatrica.

Alteration of Rod and Cone Function in Children with Usher Syndrome

C. Möller, W. Kimberling, E. Stone, 2011, European journal of ophthalmology.

Dexamethasone eye-drops for treatment of retinopathy of prematurity.

L. Gränse, H. Öhnell, S. Andreasson, 2021, Ophthalmology. Retina.

Null RPGRIP1 alleles in patients with Leber congenital amaurosis.

T. L. McGee, J. Grimsby, T. Dryja, 2001, American journal of human genetics.

Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.

Silvio Alessandro Di Gioia, Y. Arsenijévic, R. Roepman, 2016, American journal of human genetics.

Genotype-phenotype Correlations, and Retinal Function and Structure in von Hippel-Lindau Disease

M. Nordling, Elisabeth Wittström, S. Andreasson, 2014, Ophthalmic genetics.

Distribution of Cottus poecilopus Heckel and C. gobio L (Pisces) in Scandinavia

S. Andreasson, 1972 .

Locomotory Activity Patterns of Cottus poecilopus Heckel and C. gobio L. (Pisces)

S. Andreasson, 1969 .

Full‐field electroretinogram in a patient with cutaneous melanoma‐associated retinopathy

B. Ehinger, V. Ponjavic, S. Andreasson, 1993, Acta ophthalmologica.

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

R. Stevenson, C. Schwartz, D. Barker, 1995, Journal of medical genetics.

Xq 22 . fractures , and mental deficiency is linked to syndrome with blindness , dystonia , A new X linked recessive deafness

R. Stevenson, C. Schwartz, H. Lubs, 2022 .

Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene.

P. Veiga-Crespo, P. Ekström, U. Kjellström, 2016, Investigative ophthalmology & visual science.

Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1).

M. Abrahamson, S. Andréasson, L. Eksandh, 2001, Acta ophthalmologica Scandinavica.

Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

C. Möller, F. Cremers, A. Puschmann, 2019, Parkinsonism & related disorders.

Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).

M. Abrahamson, V. Ponjavic, Patrik Schatz, 2003, Acta ophthalmologica Scandinavica.

Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene

M. Abrahamson, L. Gränse, V. Ponjavic, 2001, Ophthalmic genetics.

Experimental vitreous tamponade using polyalkylimide hydrogel

F. Ghosh, S. Crafoord, S. Andreasson, 2011, Graefe's Archive for Clinical and Experimental Ophthalmology.

Successful Management of Secondary Iris Cysts With Viscoelastic-Assisted Endophotocoagulation

F. Ghosh, C. Vijayasarathy, S. Kjellstrom, 2016 .

Alteration of vitreal retinoschisin level in human primary retinal detachment.

F. Ghosh, C. Vijayasarathy, S. Kjellström, 2014, JAMA ophthalmology.

Long-term 12 year follow-up of X-linked congenital retinoschisis

P. Sieving, S. Andréasson, C. Vijayasarathy, 2010, Ophthalmic genetics.

Full-field ERG and visual fields in patients 5 years after discontinuing vigabatrin therapy

M. Lövestam-Adrian, V. Ponjavic, U. Kjellström, 2008, Documenta Ophthalmologica.

Electrophysiological evaluation of retinal function in children receiving vigabatrin medication.

V. Ponjavic, U. Kjellström, S. Andreasson, 2011, Journal of pediatric ophthalmology and strabismus.

Retinal Function in Rabbits Does Not Improve 4–5 Months after Terminating Treatment with Vigabatrin

S. Kjellström, V. Ponjavic, U. Kjellström, 2006, Documenta Ophthalmologica.

Full-field electroretinography and marked variability in clinical phenotype of Alström syndrome.

J. Naggert, C. Möller, P. Nishina, 2008, Archives of ophthalmology.

Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients.

T. Rosenberg, F. Cremers, H. Ropers, 1994, Human molecular genetics.

Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial.

B. Wilhelm, E. Zrenner, T. Rosenberg, 2020, JAMA ophthalmology.

Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1

S. Ekvall, M. Bondeson, V. Ponjavic, 2011, Ophthalmic genetics.

Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy

S. Berland, D. Austeng, C. Bredrup, 2016, Ophthalmic genetics.

Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2

N. Dahl, J. Klar, V. Ponjavic, 2006, Ophthalmic genetics.

Best’s vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene

C. Wadelius, S. Andréasson, L. Eksandh, 2001, Ophthalmic genetics.

Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.

M. Larsen, D. Sharon, S. Andréasson, 2010, Investigative ophthalmology & visual science.

Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)

L. Gränse, V. Ponjavic, T. Hugosson, 2009, Ophthalmic genetics.

Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open‐angle glaucoma and neovascular glaucoma

M. Lövestam-Adrian, J. Larsson, V. Ponjavic, 2010, Acta ophthalmologica.

Fluorescein angiography versus ERG for predicting the prognosis in central retinal vein occlusion.

J. Larsson, B. Bauer, S. Andreasson, 1998, Acta ophthalmologica Scandinavica.

Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.

A. Swaroop, R. Fujita, M. Abrahamson, 1997, American journal of ophthalmology.

Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

C. Möller, M. Koenig, D. Lacombe, 2017, Neurobiology of Disease.

Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

C. Möller, W. Kimberling, V. Ponjavic, 2011, Ophthalmic genetics.

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

P. Sieving, S. Jacobson, A. Swaroop, 1997, American journal of human genetics.

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.

P. Sieving, S. Jacobson, A. Swaroop, 1997, American journal of human genetics.

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.

P. Sieving, S. Schwartz, S. Jacobson, 2012, Investigative ophthalmology & visual science.

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

A. Swaroop, D. Breuer, B. Yashar, 2003, Ophthalmic genetics.

X-Linked Retinitis Pigmentosa: Current Status

P. Sieving, S. Jacobson, A. Swaroop, 2001 .

Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135-Trp). Disease phenotype in a Swedish family.

M. Abrahamson, B. Ehinger, V. Ponjavic, 2009, Acta ophthalmologica Scandinavica.

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

M. Abrahamson, B. Ehinger, G. Fex, 1992, Ophthalmic paediatrics and genetics.

Serum retinoids in retinitis pigmentosa patients treated with vitamin A

B. Ehinger, G. Fex, S. Andreasson, 1996, Graefe's Archive for Clinical and Experimental Ophthalmology.

X-linked retinitis pigmentosa: New map studies of XLRP2, and a possible human centromere effect

M. Warburg, T. Kruse, U. Friedrich, 1992, Human Genetics.

Genetic mapping of loci for X‐linked retinitis pigmentosa

M. Sundvall, U. Pettersson, M. Anvret, 1991, Clinical genetics.

Clinical Phenotype in a Swedish Family with a Mutation in the IMPDH1 Gene

T. L. McGee, T. Dryja, M. Abrahamson, 2005, Ophthalmic genetics.

Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system.

P. Nilsson-ehle, M. Abrahamson, B. Ehinger, 1998, Molecular pathology : MP.

Region but Splice Defects in Two Families

P. Sieving, S. Jacobson, R. Fujita, 2006 .

Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR gene.

A. Swaroop, R. Fujita, M. Abrahamson, 1998, Investigative ophthalmology & visual science.

Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.

A. Swaroop, R. Fujita, M. Abrahamson, 1998, Ophthalmic genetics.

Autoantibodies against bestrophin in a patient with vitelliform paraneoplastic retinopathy and a metastatic choroidal malignant melanoma.

G. Adamus, S. Andreasson, L. Eksandh, 2008, Archives of ophthalmology.

Improved retinal function after trabeculectomy in glaucoma patients

M. Lövestam-Adrian, V. Ponjavic, Patrik Schatz, 2009, Graefe's Archive for Clinical and Experimental Ophthalmology.

Photopic 30 Hz flicker ERG as a predictor for rubeosis in central retinal vein occlusion

J. Larsson, S. Andreasson, 2001, British Journal of Ophthalmology.

Multifocal electroretinogram for functional evaluation of retinal injury following ischemia–reperfusion in pigs

S. Andréasson, Bodil Gesslein, M. Malmsjö, 2009, Graefe's Archive for Clinical and Experimental Ophthalmology.

RETINAL FUNCTION AFTER SCLERAL BUCKLING FOR RECENT ONSET RHEGMATOGENOUS RETINAL DETACHMENT: Assessment With Electroretinography and Optical Coherence Tomography

K. Holm, Patrik Schatz, S. Andreasson, 2007, Retina.

Clinical and Electrophysiologic Outcome in Patients with Neovascular Glaucoma Treated with and without Bevacizumab

H. Holmberg, C. Hvarfner, Elisabeth Wittström, 2012, European journal of ophthalmology.

The porcine retinal vasculature accessed using an endovascular approach: a new experimental model for retinal ischemia.

Bodil Gesslein, M. Malmsjö, Håkan Morén, 2009, Investigative ophthalmology & visual science.

MULTIFOCAL ELECTRORETINOGRAPHY AND FLUORESCEIN ANGIOGRAPHY IN RETINAL VEIN OCCLUSION

S. Andréasson, J. Larsson, C. Hvarfner, 2006, Retina.

The 30-Hz flicker cone ERG for monitoring the early course of central retinal vein occlusion.

J. Larsson, B. Bauer, S. Andreasson, 2000, Acta ophthalmologica Scandinavica.

Cone b-wave implicit time as an early predictor of rubeosis in central retinal vein occlusion.

J. Larsson, B. Bauer, S. Andreasson, 1998, American journal of ophthalmology.

Intravitreal Injection of Triamcinolone Acetonide into Healthy Rabbit Eyes Alters Retinal Function and Morphology

F. Ghosh, V. Ponjavic, A. C. Myers, 2013, Current eye research.

Transcutaneous oximetry but not arterial toe blood pressure or ankle-brachial index is related to macular thickness in patients with chronic diabetic foot ulcers

M. Löndahl, P. Katzman, S. Andreasson, 2013 .

Longitudinal Changes of Macular Curvature in Patients with Retinitis Pigmentosa

S. Andréasson, H. Terasaki, S. Ueno, 2020, Translational vision science & technology.

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

P. Sieving, G. Fishman, B. Yashar, 1999, Human mutation.

Electrophysiological studies in newly onset type 2 diabetes without visible vascular retinopathy

U. Lindblad, A. Melander, M. Lövestam-Adrian, 2011, Documenta Ophthalmologica.

An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS

D. Nickerson, M. Bamshad, C. Möller, 2017, Genes.

Presence of chronic diabetic foot ulcers is associated with more frequent and more advanced retinopathy

M. Löndahl, P. Katzman, S. Andreasson, 2018, Diabetic medicine : a journal of the British Diabetic Association.

Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.

P. Sieving, S. Jacobson, A. Swaroop, 2003, Molecular vision.

Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.

B. Weber, B. Wissinger, S. Andréasson, 2009, American journal of ophthalmology.

Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.

A. Swaroop, J. Friedman, M. Abrahamson, 2010, Archives of ophthalmology.

Macular function assessed with mfERG before and after panretinal photocoagulation in patients with proliferative diabetic retinopathy

M. Lövestam-Adrian, V. Ponjavic, S. Andreasson, 2004, Documenta Ophthalmologica.

Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa

S. Andréasson, V. Ponjavic, U. Kjellström, 2016, Molecular vision.

A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing

L. Gränse, S. Kjellström, U. Kjellström, 2023, Genes.

Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?

T. Säll, A. Puschmann, Efthymia Kafantari, 2020, Parkinsonism & related disorders.

Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy.

S. Andréasson, U. Eriksson, V. Ponjavic, 2004, Acta ophthalmologica Scandinavica.

Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.

L. Gränse, V. Ponjavic, S. Andreasson, 2004, Acta ophthalmologica Scandinavica.

ELECTROPHYSIOLOGICAL ASSESSMENT OF RETINAL FUNCTION DURING 6 MONTHS OF BEVACIZUMAB TREATMENT IN NEOVASCULAR AGE-RELATED MACULAR DEGENERATION

A. Sjølie, S. Andréasson, K. B. Pedersen, 2010, Retina.

Full-field electroretinograms in patients with the carbohydrate-deficient glycoprotein syndrome.

B. Ehinger, K. Strömland, G. Blennow, 1991, American journal of ophthalmology.

Angiography and multifocal electroretinography show that blood supply to the pig retina may be both ipsilateral and contralateral.

Bodil Gesslein, M. Malmsjö, Håkan Morén, 2013, Investigative ophthalmology & visual science.

Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab

F. Ghosh, V. Ponjavic, A. C. Myers, 2014, Current eye research.

A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa

C. Rivolta, P. Farinelli, A. Superti-Furga, 2019, Ophthalmic genetics.

Retinal function and histopathology in rabbits treated with Topiramate

T. Eriksson, V. Ponjavic, S. Kjellstrom, 2006, Documenta Ophthalmologica.

Genotype and Phenotype in an unusual form of Laurence–Moon–Bardet–Biedl syndrome

T. Strom, N. Weisschuh, S. Andreasson, 2016, Acta ophthalmologica.

Multifocal electroretinogram in branch retinal vein occlusion.

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Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.

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Locomotory activity patterns of Cottus poecilopus Heckel

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Retinal Function and Morphology in Rabbit After Intravitreal Injection of VEGF Inhibitors

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A novel phenotype associated with the R162W variant in the KCNJ13 gene

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Cerebral Functional Magnetic Resonance Imaging and Multifocal Visual Evoked Potentials in a Patient with Unexplained Impairment of Visual Function: A Case Report

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Multifocal visual evoked potentials—a method study of responses from small sectors of the visual field

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Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.

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