Wissinger B - Search Results

1

A clinical and molecular genetic study of German patients with primary congenital glaucoma.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Among authors: wissinger b. Am J Ophthalmol. 2009 Apr;147(4):744-53. doi: 10.1016/j.ajo.2008.11.008. Epub 2009 Feb 4. Am J Ophthalmol. 2009. PMID: 19195637

2

Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients.

Weisschuh N, Neumann D, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Among authors: wissinger b. Mol Vis. 2005 Apr 18;11:284-7. Mol Vis. 2005. PMID: 15851979 Free article.

3

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.

Schuster A, Weisschuh N, Jägle H, Besch D, Janecke AR, Zierler H, Tippmann S, Zrenner E, Wissinger B. Schuster A, et al. Among authors: wissinger b. Br J Ophthalmol. 2005 Oct;89(10):1258-64. doi: 10.1136/bjo.2004.063933. Br J Ophthalmol. 2005. PMID: 16170112 Free PMC article.

4

Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.

Weisschuh N, Dressler P, Schuettauf F, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Among authors: wissinger b. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3846-52. doi: 10.1167/iovs.06-0343. Invest Ophthalmol Vis Sci. 2006. PMID: 16936096

5

Variations in the WDR36 gene in German patients with normal tension glaucoma.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Among authors: wissinger b. Mol Vis. 2007 May 16;13:724-9. Mol Vis. 2007. PMID: 17563723 Free PMC article.

6

Identification of genes that are linked with optineurin expression using a combined RNAi--microarray approach.

Weisschuh N, Alavi MV, Bonin M, Wissinger B. Weisschuh N, et al. Among authors: wissinger b. Exp Eye Res. 2007 Oct;85(4):450-61. doi: 10.1016/j.exer.2007.06.012. Epub 2007 Jun 27. Exp Eye Res. 2007. PMID: 17663987

7

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T. Wissinger B, et al. Invest Ophthalmol Vis Sci. 2008 Feb;49(2):751-7. doi: 10.1167/iovs.07-0471. Invest Ophthalmol Vis Sci. 2008. PMID: 18235024

8

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: wissinger b. 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.

9

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Among authors: wissinger b. Clin Genet. 2008 Nov;74(5):476-80. doi: 10.1111/j.1399-0004.2008.01025.x. Epub 2008 May 21. Clin Genet. 2008. PMID: 18498376

10

Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma.

Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N. Wolf C, et al. Among authors: wissinger b. J Glaucoma. 2010 Feb;19(2):136-41. doi: 10.1097/IJG.0b013e31819f9330. J Glaucoma. 2010. PMID: 19373106

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