V. Ponjavic

发表

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

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

Multifocal electroretinogram (mfERG) in patients with diabetes mellitus and an enlarged foveal avascular zone (FAZ)

M. Lövestam-Adrian, V. Ponjavic, M. Tyrberg, 2008, Documenta Ophthalmologica.

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.

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

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

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.

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.

Retinal function and histopathology in rabbits treated with Topiramate

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

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

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

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.

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.

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.

Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

P. Nilsson-ehle, M. Abrahamson, B. Ehinger, 1998, Ophthalmic genetics.

Function and histopathology after medication with rifabutin, inhibitors of vascular endothelial growth factors, triamcinolone and adalimumab

F. Ghosh, V. Ponjavic, 2013 .

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

Thyroid-associated ophthalmopathy after treatment for Graves' hyperthyroidism with antithyroid drugs or iodine-131.

A. Taube, G. Lundell, G. Wallin, 2009, The Journal of clinical endocrinology and metabolism.

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.

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.

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.

Alteration of Rod and Cone Function in Children with Usher Syndrome

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

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 .

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.

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.

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

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

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.

Multifocal Electroretinography (mfERG) in Insulin Dependent Diabetics with and without Clinically Apparent Retinopathy

M. Lövestam-Adrian, V. Ponjavic, M. Tyrberg, 2005, Documenta Ophthalmologica.

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.

Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

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

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.

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.

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.

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

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

Improved retinal function after trabeculectomy in glaucoma patients

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

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

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

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.

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.

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.

Using multifocal electroretinography hard exudates affect macular function in eyes with diabetic retinopathy

M. Lövestam-Adrian, K. Holm, V. Ponjavic, 2010, Graefe's Archive for Clinical and Experimental Ophthalmology.

Retinal function and histopathology in rabbits treated with Topiramate

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

RIFABUTIN ACCUMULATES IN THE LENS AND REDUCES RETINAL FUNCTION IN THE RABBIT EYE

F. Ghosh, S. Kjellström, V. Ponjavic, 2009, Retina.

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

F. Ghosh, V. Ponjavic, A. C. Myers, 2012, Current eye research.