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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1975 1
1976 1
1977 1
1986 2
1991 1
1992 4
1993 4
1994 5
1995 3
1996 1
1997 4
1998 3
1999 4
2001 3
2002 2
2003 1
2004 2
2005 4
2006 3
2007 5
2008 3
2009 7
2010 6
2011 4
2012 1
2013 4
2014 4
2015 4
2016 1
2017 2
2018 1
2019 2
2020 3
2021 1
2022 3
2023 1
2024 0

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93 results

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Page 1
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: ruther k. 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: ruther k. 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.
[Hereditary Optic Neuropathies].
Rüther K. Rüther K. Klin Monbl Augenheilkd. 2018 Jun;235(6):747-763. doi: 10.1055/a-0583-6290. Epub 2018 Feb 28. Klin Monbl Augenheilkd. 2018. PMID: 29490390 Review. German.
[Pseudotumor cerebri syndrome].
Rüther K. Rüther K. Ophthalmologe. 2014 Apr;111(4):383-94. doi: 10.1007/s00347-014-3055-7. Ophthalmologe. 2014. PMID: 24756190 German.
[Non-Arteritic Ischemic Optic Neuropathy (NAION)].
Wilhelm H, Beisse F, Rüther K. Wilhelm H, et al. Among authors: ruther k. Klin Monbl Augenheilkd. 2015 Nov;232(11):1260-9. doi: 10.1055/s-0035-1558170. Epub 2015 Nov 17. Klin Monbl Augenheilkd. 2015. PMID: 26575534 Review. German.
[Developments in ophthalmologic electrophysiology].
Rüther K, Zrenner E. Rüther K, et al. Klin Monbl Augenheilkd. 1993 Feb;202(2):140-5. doi: 10.1055/s-2008-1045575. Klin Monbl Augenheilkd. 1993. PMID: 8487470 Review. German.
[Current recommendations on optic neuritis].
Beisse F, Beisse C, Lagrèze WA, Rüther K, Schiefer U, Wilhelm H. Beisse F, et al. Among authors: ruther k. Ophthalmologe. 2014 Aug;111(8):722-6. doi: 10.1007/s00347-013-2983-y. Ophthalmologe. 2014. PMID: 25113867 German.
93 results