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Year Number of Results
2002 2
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Page 1
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.
Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, Pennesi ME, van den Born LI, Varsányi B, Szabó V, Sharon D, Banin E, Ben-Yosef T, Roosing S, Koenekoop RK, Rivolta C. Han JH, et al. Among authors: knezy k. Genet Med. 2024 Jun;26(6):101106. doi: 10.1016/j.gim.2024.101106. Epub 2024 Feb 28. Genet Med. 2024. PMID: 38420906 Free article.
[Staging of aniridia-associated keratopathy].
Náray A, Fries FN, Csidey M, Kéki-Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Csorba A, Kormányos K, Szabó D, Corton M, Tory K, Nagy ZZ, Maka E, Szentmáry N. Náray A, et al. Among authors: knezy k. Orv Hetil. 2023 Jul 9;164(27):1063-1069. doi: 10.1556/650.2023.32803. Print 2023 Jul 9. Orv Hetil. 2023. PMID: 37422887 Hungarian.
[Congenital aniridia - Hungarian data of a spectrum disease].
Náray A, Csidey M, Kéki-Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Csorba A, Kormányos K, Szabó D, Stachon T, Corton M, Tory K, Nagy ZZ, Maka E, Szentmáry N. Náray A, et al. Among authors: knezy k. Orv Hetil. 2023 Jan 29;164(4):148-155. doi: 10.1556/650.2023.32697. Print 2023 Jan 29. Orv Hetil. 2023. PMID: 36709437 Hungarian.
[Congenital aniridia patients' experience on their visual impairment in Hungary.].
Csidey M, Grupcheva C, Stachon T, Hecker D, Náray A, Kéki-Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Csorba A, Kormányos K, Szabó D, Corton M, Tory K, Nagy ZZ, Lagali N, Maka E, Szentmáry N. Csidey M, et al. Among authors: knezy k. Orv Hetil. 2023 Aug 27;164(34):1342-1349. doi: 10.1556/650.2023.32845. Print 2023 Aug 27. Orv Hetil. 2023. PMID: 37634154 Free article. Hungarian.
Examination of Subbasal Nerve Plexus and Central Corneal Stromal Microstructure in Subjects With Congenital Aniridia, Using in Vivo Confocal Laser Scanning Microscopy.
Csorba A, Kormányos K, Csidey M, Náray A, Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Szabó D, Corton M, Tory K, Nagy ZZ, Langenbucher A, Maka E, Szentmáry N. Csorba A, et al. Among authors: knezy k. Curr Eye Res. 2024 Jun;49(6):582-590. doi: 10.1080/02713683.2024.2320779. Epub 2024 Mar 5. Curr Eye Res. 2024. PMID: 38444179
Insights into eye genetics and recent advances in ocular gene therapy.
Szabó V, Varsányi B, Barboni M, Takács Á, Knézy K, Molnár MJ, Nagy ZZ, György B, Rivolta C. Szabó V, et al. Among authors: knezy k. Mol Cell Probes. 2025 Jan 18;79:102008. doi: 10.1016/j.mcp.2025.102008. Online ahead of print. Mol Cell Probes. 2025. PMID: 39805344 Free article. Review.
Examination of the Corneal Endothelium in Patients With Congenital Aniridia With a PAX6 Mutation Using In Vivo Confocal Laser Scanning Microscopy.
Csidey M, Csorba A, Kormányos K, Náray A, Kéki-Kovács K, Németh O, Knézy K, Bausz M, Szigeti A, Szabó D, Corton M, Tory K, Jávorszky E, Nagy ZZ, Maka E, Langenbucher A, Sperlich K, Stachs O, Winter K, Szentmáry N. Csidey M, et al. Among authors: knezy k. Cornea. 2024 Dec 12. doi: 10.1097/ICO.0000000000003779. Online ahead of print. Cornea. 2024. PMID: 39670973
17 results