Wilke R - Search Results

1

CERKL mutations and associated phenotypes in seven Spanish families with autosomal recessive retinitis pigmentosa.

Avila-Fernandez A, Riveiro-Alvarez R, Vallespin E, Wilke R, Tapias I, Cantalapiedra D, Aguirre-Lamban J, Gimenez A, Trujillo-Tiebas MJ, Ayuso C. Avila-Fernandez A, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2709-13. doi: 10.1167/iovs.07-0865. Invest Ophthalmol Vis Sci. 2008. PMID: 18515597

2

Mutation screening of 299 Spanish families with retinal dystrophies by Leber congenital amaurosis genotyping microarray.

Vallespin E, Cantalapiedra D, Riveiro-Alvarez R, Wilke R, Aguirre-Lamban J, Avila-Fernandez A, Lopez-Martinez MA, Gimenez A, Trujillo-Tiebas MJ, Ramos C, Ayuso C. Vallespin E, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5653-61. doi: 10.1167/iovs.07-0007. Invest Ophthalmol Vis Sci. 2007. PMID: 18055816

3

Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa.

Riveiro-Alvarez R, Vallespin E, Wilke R, Garcia-Sandoval B, Cantalapiedra D, Aguirre-Lamban J, Avila-Fernandez A, Gimenez A, Trujillo-Tiebas MJ, Ayuso C. Riveiro-Alvarez R, et al. Among authors: wilke r. Mol Vis. 2008 Feb 4;14:262-7. Mol Vis. 2008. PMID: 18334942 Free PMC article.

4

Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.

Kitiratschky VB, Wilke R, Renner AB, Kellner U, Vadalà M, Birch DG, Wissinger B, Zrenner E, Kohl S. Kitiratschky VB, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2008 Nov;49(11):5015-23. doi: 10.1167/iovs.08-1901. Epub 2008 May 16. Invest Ophthalmol Vis Sci. 2008. PMID: 18487367 Free PMC article.

5

Correlation between macular morphology and sensitivity in patients with retinitis pigmentosa and hyperautofluorescent ring.

Lenassi E, Troeger E, Wilke R, Hawlina M. Lenassi E, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2012 Jan 3;53(1):47-52. doi: 10.1167/iovs.11-8048. Invest Ophthalmol Vis Sci. 2012. PMID: 22110079

6

The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.

Schuster A, Janecke AR, Wilke R, Schmid E, Thompson DA, Utermann G, Wissinger B, Zrenner E, Gal A. Schuster A, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2007 Apr;48(4):1824-31. doi: 10.1167/iovs.06-0628. Invest Ophthalmol Vis Sci. 2007. PMID: 17389517

7

Positioning of electronic subretinal implants in blind retinitis pigmentosa patients through multimodal assessment of retinal structures.

Kusnyerik A, Greppmaier U, Wilke R, Gekeler F, Wilhelm B, Sachs HG, Bartz-Schmidt KU, Klose U, Stingl K, Resch MD, Hekmat A, Bruckmann A, Karacs K, Nemeth J, Suveges I, Zrenner E. Kusnyerik A, et al. Among authors: wilke r. Invest Ophthalmol Vis Sci. 2012 Jun 20;53(7):3748-55. doi: 10.1167/iovs.11-9409. Invest Ophthalmol Vis Sci. 2012. PMID: 22562517

8

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: wilke r. 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.

9

Two truncating USH3A mutations, including one novel, in a German family with Usher syndrome.

Ebermann I, Wilke R, Lauhoff T, Lübben D, Zrenner E, Bolz HJ. Ebermann I, et al. Among authors: wilke r. Mol Vis. 2007 Aug 30;13:1539-47. Mol Vis. 2007. PMID: 17893653

10

Basic quantitative assessment of visual performance in patients with very low vision.

Bach M, Wilke M, Wilhelm B, Zrenner E, Wilke R. Bach M, et al. Among authors: wilke r, wilke m. Invest Ophthalmol Vis Sci. 2010 Feb;51(2):1255-60. doi: 10.1167/iovs.09-3512. Epub 2009 Oct 22. Invest Ophthalmol Vis Sci. 2010. PMID: 19850846

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