Losonczy G - Search Results

1

Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombasthenia.

Losonczy G, Rosenberg N, Boda Z, Vereb G, Kappelmayer J, Hauschner H, Bereczky Z, Muszbek L. Losonczy G, et al. Haematologica. 2007 May;92(5):698-701. doi: 10.3324/haematol.10847. Haematologica. 2007. PMID: 17488698 Free article.

2

A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.

Losonczy G, Rosenberg N, Kiss C, Kappelmayer J, Vereb G, Kerényi A, Balogh I, Muszbek L. Losonczy G, et al. Thromb Haemost. 2005 May;93(5):904-9. doi: 10.1160/TH04-12-0848. Thromb Haemost. 2005. PMID: 15886807

3

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: losonczy g. Mol Vis. 2007 Oct 18;13:1976-83. Mol Vis. 2007. PMID: 17982422

4

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: losonczy g. Acta Ophthalmol. 2014 Nov;92(7):e562-8. doi: 10.1111/aos.12389. Epub 2014 Mar 16. Acta Ophthalmol. 2014. PMID: 24629050 Free article.

5

Cultivation of Human Oral Mucosal Explants on Contact Lenses.

Zsebik B, Ujlaky-Nagy L, Losonczy G, Vereb G, Takács L. Zsebik B, et al. Among authors: losonczy g. Curr Eye Res. 2017 Aug;42(8):1094-1099. doi: 10.1080/02713683.2017.1279635. Epub 2017 Mar 24. Curr Eye Res. 2017. PMID: 28339301

6

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: losonczy g. Invest Ophthalmol Vis Sci. 2011 Mar 10;52(3):1252-60. doi: 10.1167/iovs.10-5242. Invest Ophthalmol Vis Sci. 2011. PMID: 21071743

7

High frequency of factor V Leiden mutation and prothrombin 20210A variant in Romanies of Eastern Hungary.

Balogh I, Póka R, Losonczy G, Muszbek L. Balogh I, et al. Among authors: losonczy g. Thromb Haemost. 1999 Nov;82(5):1555-6. Thromb Haemost. 1999. PMID: 10595655 No abstract available.

8

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. BMC Med Genet. 2013 Jan 8;14:3. doi: 10.1186/1471-2350-14-3. BMC Med Genet. 2013. PMID: 23298237 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: losonczy g. Mol Vis. 2015 Feb 5;21:124-30. eCollection 2015. Mol Vis. 2015. PMID: 25684977 Free PMC article.

10

Relative anterior microphthalmos in oculodentodigital dysplasia.

Orosz O, Fodor M, Balogh I, Losonczy G. Orosz O, et al. Among authors: losonczy g. Indian J Ophthalmol. 2018 Feb;66(2):334-336. doi: 10.4103/ijo.IJO_756_17. Indian J Ophthalmol. 2018. PMID: 29380799 Free PMC article.

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