Ponjavic V - Search Results

1

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

Wittström E, Ekvall S, Schatz P, Bondeson ML, Ponjavic V, Andréasson S. Wittström E, et al. Among authors: ponjavic v. Ophthalmic Genet. 2011 Jun;32(2):83-96. doi: 10.3109/13816810.2010.535890. Epub 2010 Dec 30. Ophthalmic Genet. 2011. PMID: 21192766

2

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

Schatz P, Eriksson U, Ponjavic V, Andréasson S. Schatz P, et al. Among authors: ponjavic v. Acta Ophthalmol Scand. 2004 Aug;82(4):476-80. doi: 10.1111/j.1600-0420.2004.00277.x. Acta Ophthalmol Scand. 2004. PMID: 15291946 Free article.

3

Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.

Schatz P, Ponjavic V, Andréasson S, McGee TL, Dryja TP, Abrahamson M. Schatz P, et al. Among authors: ponjavic v. Ophthalmic Genet. 2005 Sep;26(3):119-24. doi: 10.1080/13816810500229090. Ophthalmic Genet. 2005. PMID: 16272056

4

Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2.

Schatz P, Klar J, Andréasson S, Ponjavic V, Dahl N. Schatz P, et al. Among authors: ponjavic v. Ophthalmic Genet. 2006 Jun;27(2):51-6. doi: 10.1080/13816810600677990. Ophthalmic Genet. 2006. PMID: 16754206

5

Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7).

Hugosson T, Gränse L, Ponjavic V, Andréasson S. Hugosson T, et al. Among authors: ponjavic v. Ophthalmic Genet. 2009 Mar;30(1):1-6. doi: 10.1080/13816810802454081. Ophthalmic Genet. 2009. PMID: 19172503

6

Improved retinal function after trabeculectomy in glaucoma patients.

Wittström E, Schatz P, Lövestam-Adrian M, Ponjavic V, Bergström A, Andréasson S. Wittström E, et al. Among authors: ponjavic v. Graefes Arch Clin Exp Ophthalmol. 2010 Apr;248(4):485-95. doi: 10.1007/s00417-009-1220-5. Epub 2009 Oct 29. Graefes Arch Clin Exp Ophthalmol. 2010. PMID: 19865823

7

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

Kjellström S, Vijayasarathy C, Ponjavic V, Sieving PA, Andréasson S. Kjellström S, et al. Among authors: ponjavic v. Ophthalmic Genet. 2010 Sep;31(3):114-25. doi: 10.3109/13816810.2010.482555. Ophthalmic Genet. 2010. PMID: 20569020 Free PMC article.

8

Phenotypes in defined genotypes including siblings with Usher syndrome.

Malm E, Ponjavic V, Möller C, Kimberling WJ, Andréasson S. Malm E, et al. Among authors: ponjavic v. Ophthalmic Genet. 2011 Jun;32(2):65-74. doi: 10.3109/13816810.2010.536064. Epub 2010 Dec 21. Ophthalmic Genet. 2011. PMID: 21174530

9

Anterior segment abnormalities and angle-closure glaucoma in a family with a mutation in the BEST1 gene and Best vitelliform macular dystrophy.

Wittström E, Ponjavic V, Bondeson ML, Andréasson S. Wittström E, et al. Among authors: ponjavic v. Ophthalmic Genet. 2011 Nov;32(4):217-27. doi: 10.3109/13816810.2011.567884. Epub 2011 Apr 7. Ophthalmic Genet. 2011. PMID: 21473666

10

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

Ponjavic V, Abrahamson M, Andréasson S, Van Bokhoven H, Cremers FP, Ehinger B, Fex G. Ponjavic V, et al. Ophthalmic Genet. 1995 Dec;16(4):143-50. doi: 10.3109/13816819509057855. Ophthalmic Genet. 1995. PMID: 8749050

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