Berta A - Search Results

1

Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma.

Losonczy G, Fazakas F, Pfliegler G, Komáromi I, Balázs E, Pénzes K, Berta A. Losonczy G, et al. Among authors: berta a. BMC Med Genet. 2013 Jan 8;14:3. doi: 10.1186/1471-2350-14-3. BMC Med Genet. 2013. PMID: 23298237 Free PMC article.

2

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

3

Bilateral central retinal vein occlusion caused by malignant hypertension in a young patient.

Balogh Z, Berta A, Pfliegler G, Nagy V. Balogh Z, et al. Among authors: berta a. Clin Exp Hypertens. 2011;33(1):53-5. doi: 10.3109/10641963.2010.503304. Epub 2010 Dec 19. Clin Exp Hypertens. 2011. PMID: 21166599 Free article.

4

Hemodynamic changes after ruthenium irradiation of Hippel's angiomatosis.

Balázs E, Berta A, Rózsa L, Kolozsvári L, Rigó G. Balázs E, et al. Among authors: berta a. Ophthalmologica. 1990;200(3):128-32. doi: 10.1159/000310093. Ophthalmologica. 1990. PMID: 2189085

5

Activated protein C resistance in anterior ischaemic optic neuropathy.

Nagy V, Facsko A, Takacs L, Balazs E, Berta A, Balogh I, Edes I, Czuriga I, Pfliegler G. Nagy V, et al. Among authors: berta a. Acta Ophthalmol Scand. 2004 Apr;82(2):140-3. doi: 10.1111/j.1600-0420.2004.00226.x. Acta Ophthalmol Scand. 2004. PMID: 15043529 Free article.

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

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.

8

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.

9

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.

10

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.

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