Lesch B - Search Results

1

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.

2

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.

3

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

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

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

6

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

7

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

8

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.

9

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.

10

Dual α-globin-truncated erythropoietin receptor knockin restores hemoglobin production in α-thalassemia-derived erythroid cells.

Chu SN, Soupene E, Sharma D, Sinha R, McCreary T, Hernandez B, Shen H, Wienert B, Bowman C, Yin H, Lesch BJ, Jia K, Romero KA, Kostamo Z, Zhang Y, Tran T, Cordero M, Homma S, Hampton JP, Gardner JM, Conklin BR, MacKenzie TC, Sheehan VA, Porteus MH, Cromer MK. Chu SN, et al. Among authors: lesch bj. Cell Rep. 2025 Jan 3;44(1):115141. doi: 10.1016/j.celrep.2024.115141. Online ahead of print. Cell Rep. 2025. PMID: 39754719 Free article.

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