Lesch B - Search Results

1

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: lesch b. Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1834-1842. doi: 10.1167/iovs.16-21405. Invest Ophthalmol Vis Sci. 2017. PMID: 28358949

2

Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genes.

Vámos R, Külm M, Szabó V, Ahman A, Lesch B, Schneider M, Varsányi B, Nagy ZZ, Németh J, Farkas Á. Vámos R, et al. Among authors: lesch b. Eur J Ophthalmol. 2016 Jan-Feb;26(1):78-84. doi: 10.5301/ejo.5000643. Epub 2015 Jul 2. Eur J Ophthalmol. 2016. PMID: 26165328

3

Truncation of retinoschisin protein associated with a novel splice site mutation in the RS1 gene.

Lesch B, Szabó V, Kánya M, Varsányi B, Somfai GM, Hargitai J, Vámos R, Fiedler O, Farkas A. Lesch B, et al. Mol Vis. 2008 Aug 25;14:1549-58. Mol Vis. 2008. PMID: 18728755 Free PMC article.

4

Role of multifocal electroretinography in the diagnosis of idiopathic macular hole.

Tuzson R, Varsanyi B, Vince Nagy B, Lesch B, Vámos R, Németh J, Farkas A, Ferencz M. Tuzson R, et al. Among authors: lesch b. Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1666-70. doi: 10.1167/iovs.09-4375. Epub 2009 Nov 11. Invest Ophthalmol Vis Sci. 2010. PMID: 19907028

5

Optical coherence tomography of the macula in congenital achromatopsia.

Varsányi B, Somfai GM, Lesch B, Vámos R, Farkas A. Varsányi B, et al. Among authors: lesch b. Invest Ophthalmol Vis Sci. 2007 May;48(5):2249-53. doi: 10.1167/iovs.06-1173. Invest Ophthalmol Vis Sci. 2007. PMID: 17460287

6

Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.

Lesch B, Szabó V, Kánya M, Somfai GM, Vámos R, Varsányi B, Pámer Z, Knézy K, Salacz G, Janáky M, Ferencz M, Hargitai J, Papp A, Farkas A. Lesch B, et al. Mol Vis. 2008;14:2321-32. Epub 2008 Dec 12. Mol Vis. 2008. PMID: 19093009 Free PMC article.

7

Stromal Cell-Derived Factor 1 Polymorphism in Retinal Vein Occlusion.

Szigeti A, Ecsedy M, Schneider M, Lénárt L, Lesch B, Nagy ZZ, Fekete A, Récsán Z. Szigeti A, et al. Among authors: lesch b. PLoS One. 2016 Nov 10;11(11):e0166544. doi: 10.1371/journal.pone.0166544. eCollection 2016. PLoS One. 2016. PMID: 27832196 Free PMC article.

8

Functional assessment of the possible toxicity of indocyanine green dye in macular hole surgery.

Ferencz M, Somfai GM, Farkas A, Kovács I, Lesch B, Récsán Z, Nemes J, Salacz G. Ferencz M, et al. Among authors: lesch b. Am J Ophthalmol. 2006 Nov;142(5):765-70. doi: 10.1016/j.ajo.2006.05.054. Am J Ophthalmol. 2006. PMID: 17056360

9

TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness.

Maasz A, Hadzsiev K, Ripszam R, Zsigmond A, Maka E, Knezy K, Lesch B, Nemeth A, Bene J, Galik B, Gyenesei A, Melegh B. Maasz A, et al. Among authors: lesch b. Eur J Med Genet. 2022 Apr;65(4):104471. doi: 10.1016/j.ejmg.2022.104471. Epub 2022 Feb 28. Eur J Med Genet. 2022. PMID: 35240325 Free article.

10

Combining Cell-Intrinsic and -Extrinsic Resistance to HIV-1 By Engineering Hematopoietic Stem Cells for CCR5 Knockout and B Cell Secretion of Therapeutic Antibodies.

Feist WN, Luna SE, Ben-Efraim K, Filsinger Interrante MV, Amorin NA, Johnston NM, Bruun TUJ, Ghanim HY, Lesch BJ, Dudek AM, Porteus MH. Feist WN, et al. Among authors: lesch bj. bioRxiv [Preprint]. 2024 Mar 9:2024.03.08.583956. doi: 10.1101/2024.03.08.583956. bioRxiv. 2024. PMID: 38496600 Free PMC article. Preprint.

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