Berger W - Search Results

1

ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotype.

Poloschek CM, Bach M, Lagrèze WA, Glaus E, Lemke JR, Berger W, Neidhardt J. Poloschek CM, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2010 Aug;51(8):4253-65. doi: 10.1167/iovs.09-4655. Epub 2010 Mar 24. Invest Ophthalmol Vis Sci. 2010. PMID: 20335603 Free article.

2

Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene.

Ruether K, van de Pol D, Jaissle G, Berger W, Tornow RP, Zrenner E. Ruether K, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 1997 Mar;38(3):710-8. Invest Ophthalmol Vis Sci. 1997. PMID: 9071226

3

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W. Zeitz C, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4328-35. doi: 10.1167/iovs.05-0526. Invest Ophthalmol Vis Sci. 2005. PMID: 16249515

4

Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.

Neidhardt J, Barthelmes D, Farahmand F, Fleischhauer JC, Berger W. Neidhardt J, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1630-5. doi: 10.1167/iovs.05-1317. Invest Ophthalmol Vis Sci. 2006. PMID: 16565402

5

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: berger w. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3523-30. doi: 10.1167/iovs.06-0271. Invest Ophthalmol Vis Sci. 2006. PMID: 16877424

6

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: berger w. 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.

7

Identification and characterization of a novel RPGR isoform in human retina.

Neidhardt J, Glaus E, Barthelmes D, Zeitz C, Fleischhauer J, Berger W. Neidhardt J, et al. Among authors: berger w. Hum Mutat. 2007 Aug;28(8):797-807. doi: 10.1002/humu.20521. Hum Mutat. 2007. PMID: 17405150

8

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.

Zeitz C, Gross AK, Leifert D, Kloeckener-Gruissem B, McAlear SD, Lemke J, Neidhardt J, Berger W. Zeitz C, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):4105-14. doi: 10.1167/iovs.08-1717. Epub 2008 May 16. Invest Ophthalmol Vis Sci. 2008. PMID: 18487375

9

Syndromic choroideremia: sublocalization of phenotypes associated with Martin-Probst deafness mental retardation syndrome.

Poloschek CM, Kloeckener-Gruissem B, Hansen LL, Bach M, Berger W. Poloschek CM, et al. Among authors: berger w. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):4096-104. doi: 10.1167/iovs.08-2044. Epub 2008 May 16. Invest Ophthalmol Vis Sci. 2008. PMID: 18487380

10

Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled-4.

Luhmann UF, Neidhardt J, Kloeckener-Gruissem B, Schäfer NF, Glaus E, Feil S, Berger W. Luhmann UF, et al. Among authors: berger w. Eur J Neurosci. 2008 May;27(10):2619-28. doi: 10.1111/j.1460-9568.2008.06237.x. Eur J Neurosci. 2008. PMID: 18547247 Free article.

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