G. Losonczy

发表

Effects of aging on corneal parameters measured with Pentacam in healthy subjects

G. Nemeth, Z. Hassan, G. Vitályos, 2019, Scientific Reports.

Tear Mediators NGF along with IL-13 Predict Keratoconus Progression

P. Gogolák, Z. Hassan, G. Vitályos, 2020, Ocular immunology and inflammation.

Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene

A. Berta, I. Balogh, Attila Vajas, 2015, Molecular vision.

Femtosecond laser-assisted keratoplasty combined with cataract extraction in a patient with keratoconus and oculocutaneous albinism

B. Kolozsvári, G. Losonczy, Dorottya Pásztor, 2016, Indian journal of ophthalmology.

ADAMTS9 locus associates with increased risk of wet AMD

I. Immonen, M. Uusitupa, M. Hiltunen, 2014, Acta ophthalmologica.

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

G. Vereb, N. Rosenberg, H. Hauschner, 2007, Haematologica.

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

A. Berta, G. Losonczy, L. Takács, 2015, International journal of ophthalmology.

Detection of factor XIII‐A is a valuable tool for distinguishing dendritic cells and tissue macrophages in granuloma annulare and necrobiosis lipoidica

R. Ádány, É. Remenyik, B. Dezső, 2014, Journal of the European Academy of Dermatology and Venereology : JEADV.

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

G. Vereb, A. Berta, I. Balogh, 2007, Molecular vision.

Segregation analysis suggests that keratoconus is a complex non‐mendelian disease

G. Vereb, A. Berta, G. Losonczy, 2014, Acta ophthalmologica.

Correction of irregular and induced regular corneal astigmatism with toric IOL after posterior segment surgery: a case series

B. Kolozsvári, G. Losonczy, Dorottya Pásztor, 2017, BMC Ophthalmology.

Cultivation of Human Oral Mucosal Explants on Contact Lenses

G. Vereb, G. Losonczy, B. Zsebik, 2017, Current eye research.

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

I. Komáromi, E. Balázs, A. Berta, 2013, BMC Medical Genetics.

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

V. Beneš, G. Vereb, A. Berta, 2011, Investigative ophthalmology & visual science.

Nivolumab-Induced Ulcerative Keratitis—A Case Report

R. Nuijts, G. Losonczy, M. Gijs, 2020, Cornea.

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

I. Rajta, M. Resch, A. Berta, 2017, Investigative ophthalmology & visual science.

Effect of the Gas6 c.834+7G>A Polymorphism and the Interaction of Known Risk Factors on AMD Pathogenesis in Hungarian Patients

Á. Fekete, A. Berta, É. Ajzner, 2012, PloS one.

Low prevalence of spectacle use in the Hungarian Roma population indicates unmet health needs

B. J. Klevering, R. Ádány, J. Sándor, 2022, Scientific Reports.

Unmet Health Need Among Roma: Visual Acuity and the Use of Vision Correcting Aids in the Hungarian Roma Population

B. J. Klevering, R. Ádány, J. Sándor, 2022 .

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

Á. Fekete, A. Berta, É. Ajzner, 2011, Acta ophthalmologica.