Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

275 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Evidence-based diagnostic approach to inherited retinal dystrophies 2009].
Kellner U, Kellner S, Renner AB, Fiebig BS, Weinitz S, Weber BH. Kellner U, et al. Among authors: kellner s. Klin Monbl Augenheilkd. 2009 Dec;226(12):999-1011. doi: 10.1055/s-0028-1109684. Epub 2009 Sep 15. Klin Monbl Augenheilkd. 2009. PMID: 19757352 Review. German.
[Inherited retinal or optic nerve disorders – five steps to diagnosis].
Kellner U, Kellner S, Weinitz S, Farmand G, Weber BH, Stöhr H. Kellner U, et al. Among authors: kellner s. Klin Monbl Augenheilkd. 2015 Mar;232(3):250-8. doi: 10.1055/s-0034-1396211. Epub 2015 Mar 24. Klin Monbl Augenheilkd. 2015. PMID: 25803554 Review. German.
[Hereditary Macular Dystrophies].
Renner AB, Kellner U. Renner AB, et al. Among authors: kellner u. Klin Monbl Augenheilkd. 2016 Oct;233(10):1124-1141. doi: 10.1055/s-0042-100474. Epub 2016 Jul 6. Klin Monbl Augenheilkd. 2016. PMID: 27385259 Review. German.
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Schulz HL, Grassmann F, Kellner U, Spital G, Rüther K, Jägle H, Hufendiek K, Rating P, Huchzermeyer C, Baier MJ, Weber BH, Stöhr H. Schulz HL, et al. Among authors: kellner u. Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):394-403. doi: 10.1167/iovs.16-19936. Invest Ophthalmol Vis Sci. 2017. PMID: 28118664 Free PMC article.
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Khan M, Cornelis SS, Pozo-Valero MD, Whelan L, Runhart EH, Mishra K, Bults F, AlSwaiti Y, AlTalbishi A, De Baere E, Banfi S, Banin E, Bauwens M, Ben-Yosef T, Boon CJF, van den Born LI, Defoort S, Devos A, Dockery A, Dudakova L, Fakin A, Farrar GJ, Sallum JMF, Fujinami K, Gilissen C, Glavač D, Gorin MB, Greenberg J, Hayashi T, Hettinga YM, Hoischen A, Hoyng CB, Hufendiek K, Jägle H, Kamakari S, Karali M, Kellner U, Klaver CCW, Kousal B, Lamey TM, MacDonald IM, Matynia A, McLaren TL, Mena MD, Meunier I, Miller R, Newman H, Ntozini B, Oldak M, Pieterse M, Podhajcer OL, Puech B, Ramesar R, Rüther K, Salameh M, Salles MV, Sharon D, Simonelli F, Spital G, Steehouwer M, Szaflik JP, Thompson JA, Thuillier C, Tracewska AM, van Zweeden M, Vincent AL, Zanlonghi X, Liskova P, Stöhr H, Roach JN, Ayuso C, Roberts L, Weber BHF, Dhaenens CM, Cremers FPM. Khan M, et al. Among authors: kellner u. Genet Med. 2020 Jul;22(7):1235-1246. doi: 10.1038/s41436-020-0787-4. Epub 2020 Apr 20. Genet Med. 2020. PMID: 32307445 Free article.
275 results