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A new mutation in enhanced S-cone syndrome.
Termühlen J, Alex AF, Glöckle N, Kellner U, Fiedler B, Eter N, Uhlig CE. Termühlen J, et al. Among authors: kellner u. Acta Ophthalmol. 2018 Jun;96(4):e539-e540. doi: 10.1111/aos.13205. Epub 2016 Aug 29. Acta Ophthalmol. 2018. PMID: 27573156 Free article. No abstract available.
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
Weisschuh N, Mayer AK, Strom TM, Kohl S, Glöckle N, Schubach M, Andreasson S, Bernd A, Birch DG, Hamel CP, Heckenlively JR, Jacobson SG, Kamme C, Kellner U, Kunstmann E, Maffei P, Reiff CM, Rohrschneider K, Rosenberg T, Rudolph G, Vámos R, Varsányi B, Weleber RG, Wissinger B. Weisschuh N, et al. Among authors: kellner u. PLoS One. 2016 Jan 14;11(1):e0145951. doi: 10.1371/journal.pone.0145951. eCollection 2016. PLoS One. 2016. PMID: 26766544 Free PMC article.
[Clinical findings and diagnostics of cone dystrophy].
Kellner U, Kellner S. Kellner U, et al. Among authors: kellner s. Ophthalmologe. 2009 Feb;106(2):99-108. doi: 10.1007/s00347-008-1863-3. Ophthalmologe. 2009. PMID: 19190919 Review. German.
Selective cone dystrophy with protan genotype.
Kellner U, Sadowski B, Zrenner E, Foerster MH. Kellner U, et al. Invest Ophthalmol Vis Sci. 1995 Nov;36(12):2381-7. Invest Ophthalmol Vis Sci. 1995. PMID: 7591627
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, Swaroop A. Wright AF, et al. Among authors: kellner u. Hum Mutat. 2004 Nov;24(5):439. doi: 10.1002/humu.9285. Hum Mutat. 2004. PMID: 15459973
275 results