Berta A - Search Results

1

Presence of Fleischer ring and prominent corneal nerves in keratoconus relatives and normal controls.

Kriszt Á, Losonczy G, Berta A, Takács L. Kriszt Á, et al. Among authors: berta a. Int J Ophthalmol. 2015 Oct 18;8(5):922-7. doi: 10.3980/j.issn.2222-3959.2015.05.12. eCollection 2015. Int J Ophthalmol. 2015. PMID: 26558202 Free PMC article.

2

Differentially expressed genes associated with human limbal epithelial phenotypes: new molecules that potentially facilitate selection of stem cell-enriched populations.

Takács L, Tóth E, Losonczy G, Szanto A, Bähr-Ivacevic T, Benes V, Berta A, Vereb G. Takács L, et al. Among authors: berta a. Invest Ophthalmol Vis Sci. 2011 Mar 10;52(3):1252-60. doi: 10.1167/iovs.10-5242. Invest Ophthalmol Vis Sci. 2011. PMID: 21071743

3

Segregation analysis suggests that keratoconus is a complex non-mendelian disease.

Kriszt A, Losonczy G, Berta A, Vereb G, Takács L. Kriszt A, et al. Among authors: berta a. Acta Ophthalmol. 2014 Nov;92(7):e562-8. doi: 10.1111/aos.12389. Epub 2014 Mar 16. Acta Ophthalmol. 2014. PMID: 24629050 Free article.

4

Myopia and Late-Onset Progressive Cone Dystrophy Associate to LVAVA/MVAVA Exon 3 Interchange Haplotypes of Opsin Genes on Chromosome X.

Orosz O, Rajta I, Vajas A, Takács L, Csutak A, Fodor M, Kolozsvári B, Resch M, Sényi K, Lesch B, Szabó V, Berta A, Balogh I, Losonczy G. Orosz O, et al. Among authors: berta a. Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1834-1842. doi: 10.1167/iovs.16-21405. Invest Ophthalmol Vis Sci. 2017. PMID: 28358949

5

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

Takács L, Losonczy G, Matesz K, Balogh I, Sohajda Z, Tóth K, Fazakas F, Vereb G, Berta A. Takács L, et al. Among authors: berta a. Mol Vis. 2007 Oct 18;13:1976-83. Mol Vis. 2007. PMID: 17982422

6

Thrombophilic screening in retinal artery occlusion patients.

Nagy V, Takacs L, Steiber Z, Pfliegler G, Berta A. Nagy V, et al. Among authors: berta a. Clin Ophthalmol. 2008 Sep;2(3):557-61. doi: 10.2147/opth.s1512. Clin Ophthalmol. 2008. PMID: 19668753 Free PMC article.

7

Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age-related macular degeneration in Hungarian patients.

Losonczy G, Fekete Á, Vokó Z, Takács L, Káldi I, Ajzner É, Kasza M, Vajas A, Berta A, Balogh I. Losonczy G, et al. Among authors: berta a. Acta Ophthalmol. 2011 May;89(3):255-62. doi: 10.1111/j.1755-3768.2009.01687.x. Acta Ophthalmol. 2011. PMID: 19845562 Free article.

8

Effect of the Gas6 c.834+7G>A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patients.

Losonczy G, Vajas A, Takács L, Dzsudzsák E, Fekete A, Márhoffer E, Kardos L, Ajzner E, Hurtado B, de Frutos PG, Berta A, Balogh I. Losonczy G, et al. Among authors: berta a. PLoS One. 2012;7(11):e50181. doi: 10.1371/journal.pone.0050181. Epub 2012 Nov 29. PLoS One. 2012. PMID: 23209669 Free PMC article.

9

Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.

Orosz O, Czeglédi M, Kántor I, Balogh I, Vajas A, Takács L, Berta A, Losonczy G. Orosz O, et al. Among authors: berta a. Mol Vis. 2015 Feb 5;21:124-30. eCollection 2015. Mol Vis. 2015. PMID: 25684977 Free PMC article.

10

Expression of betaig-h3 is lower than normal in keratoconus corneas but increases with scarring.

Takács L, Csutak A, Balázs E, Módis L Jr, Berta A. Takács L, et al. Among authors: berta a. Cornea. 1999 Sep;18(5):599-605. Cornea. 1999. PMID: 10487436

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