Feil S - Search Results

1

Genotype-phenotype spectrum in isolated and syndromic nanophthalmos.

Lang E, Koller S, Atac D, Pfäffli OA, Hanson JVM, Feil S, Bähr L, Bahr A, Kottke R, Joset P, Fasler K, Barthelmes D, Steindl K, Konrad D, Wille DA, Berger W, Gerth-Kahlert C. Lang E, et al. Among authors: feil s. Acta Ophthalmol. 2021 Jun;99(4):e594-e607. doi: 10.1111/aos.14615. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996714 Free article.

2

Intrafamilial variability of the ocular phenotype in a Polish family with a missense mutation (A63D) in the Norrie disease gene.

Zaremba J, Feil S, Juszko J, Myga W, van Duijnhoven G, Berger W. Zaremba J, et al. Among authors: feil s. Ophthalmic Genet. 1998 Sep;19(3):157-64. doi: 10.1076/opge.19.3.157.2184. Ophthalmic Genet. 1998. PMID: 9810571

3

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2).

Rosenberg T, Schwahn U, Feil S, Berger W. Rosenberg T, et al. Among authors: feil s. Ophthalmic Genet. 1999 Sep;20(3):161-72. doi: 10.1076/opge.20.3.161.2278. Ophthalmic Genet. 1999. PMID: 10520237

4

NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.

Zeitz C, Scherthan H, Freier S, Feil S, Suckow V, Schweiger S, Berger W. Zeitz C, et al. Among authors: feil s. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4184-91. doi: 10.1167/iovs.03-0251. Invest Ophthalmol Vis Sci. 2003. PMID: 14507859 Free article.

5

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

Zeitz C, Minotti R, Feil S, Mátyás G, Cremers FP, Hoyng CB, Berger W. Zeitz C, et al. Among authors: feil s. Mol Vis. 2005 Mar 2;11:179-83. Mol Vis. 2005. PMID: 15761389 Free article.

6

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.

Wycisk KA, Budde B, Feil S, Skosyrski S, Buzzi F, Neidhardt J, Glaus E, Nürnberg P, Ruether K, Berger W. Wycisk KA, et al. Among authors: feil s. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3523-30. doi: 10.1167/iovs.06-0271. Invest Ophthalmol Vis Sci. 2006. PMID: 16877424

7

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.

Wycisk KA, Zeitz C, Feil S, Wittmer M, Forster U, Neidhardt J, Wissinger B, Zrenner E, Wilke R, Kohl S, Berger W. Wycisk KA, et al. Among authors: feil s. Am J Hum Genet. 2006 Nov;79(5):973-7. doi: 10.1086/508944. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033974 Free PMC article.

8

Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.

Neidhardt J, Glaus E, Lorenz B, Netzer C, Li Y, Schambeck M, Wittmer M, Feil S, Kirschner-Schwabe R, Rosenberg T, Cremers FP, Bergen AA, Barthelmes D, Baraki H, Schmid F, Tanner G, Fleischhauer J, Orth U, Becker C, Wegscheider E, Nürnberg G, Nürnberg P, Bolz HJ, Gal A, Berger W. Neidhardt J, et al. Among authors: feil s. Mol Vis. 2008 Jun 6;14:1081-93. Mol Vis. 2008. PMID: 18552978 Free PMC article.

9

Differential gene expression in Ndph-knockout mice in retinal development.

Schäfer NF, Luhmann UF, Feil S, Berger W. Schäfer NF, et al. Among authors: feil s. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):906-16. doi: 10.1167/iovs.08-1731. Epub 2008 Oct 31. Invest Ophthalmol Vis Sci. 2009. PMID: 18978344 Free article.

10

Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgrounds.

Brunner S, Skosyrski S, Kirschner-Schwabe R, Knobeloch KP, Neidhardt J, Feil S, Glaus E, Luhmann UF, Rüther K, Berger W. Brunner S, et al. Among authors: feil s. Invest Ophthalmol Vis Sci. 2010 Feb;51(2):1106-15. doi: 10.1167/iovs.08-2742. Epub 2009 Dec 10. Invest Ophthalmol Vis Sci. 2010. PMID: 20007830 Free article.

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