S. Andréasson

发表

Multifocal Visual Evoked Potentials (mfVEP) in Diabetic Patients with and without Polyneuropathy

M. Lövestam-Adrian, L. Gränse, G. Andersson, 2012, The open ophthalmology journal.

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.

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.

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.

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.

Longitudinal Changes of Macular Curvature in Patients with Retinitis Pigmentosa

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

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.

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.

Fixation stability and implication for multifocal electroretinography in patients with neovascular age-related macular degeneration after anti-VEGF treatment

A. Sjølie, S. Andréasson, K. B. Pedersen, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

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.

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

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

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.

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.

MULTIFOCAL ELECTRORETINOGRAPHY AND FLUORESCEIN ANGIOGRAPHY IN RETINAL VEIN OCCLUSION

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

mfERG in normal and lesioned rabbit retina

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

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

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

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

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

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

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

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.

Multifocal electroretinogram in branch retinal vein occlusion.

S. Andréasson, J. Larsson, C. Hvarfner, 2003, American journal of ophthalmology.

Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin.

L. Gränse, S. Andréasson, V. Ponjavic, 2002, Acta ophthalmologica Scandinavica.

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

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

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

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

Standardized full-field electroretinography in rabbits

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

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.

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

Marie Bengtsson, G. Andersson, S. Andréasson, 2005, Clinical Neurophysiology.

Locomotory activity patterns of Cottus poecilopus Heckel

S. Andréasson, S. Andreasson, 1969 .

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.

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.

Region but Splice Defects in Two Families

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