Zrenner E - Search Results

1

Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects.

Besch D, Jägle H, Scholl HP, Seeliger MW, Zrenner E. Besch D, et al. Among authors: zrenner e. Vision Res. 2003 Dec;43(28):3095-108. doi: 10.1016/j.visres.2003.09.020. Vision Res. 2003. PMID: 14611947 Free article. Review.

2

Quantifying fixation in patients with Stargardt disease.

Reinhard J, Messias A, Dietz K, Mackeben M, Lakmann R, Scholl HP, Apfelstedt-Sylla E, Weber BH, Seeliger MW, Zrenner E, Trauzettel-Klosinski S. Reinhard J, et al. Among authors: zrenner e. Vision Res. 2007 Jul;47(15):2076-85. doi: 10.1016/j.visres.2007.04.012. Epub 2007 Jun 11. Vision Res. 2007. PMID: 17562343 Free article.

3

Mapping of retinal function in Best macular dystrophy using multifocal electroretinography.

Scholl HP, Schuster AM, Vonthein R, Zrenner E. Scholl HP, et al. Among authors: zrenner e. Vision Res. 2002 Apr;42(8):1053-61. doi: 10.1016/s0042-6989(02)00034-2. Vision Res. 2002. PMID: 11934455 Free article.

4

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E. Langrová H, et al. Among authors: zrenner e. Vision Res. 2002 May;42(11):1475-83. doi: 10.1016/s0042-6989(02)00068-8. Vision Res. 2002. PMID: 12044753 Free article.

5

Spatial cone activity distribution in diseases of the posterior pole determined by multifocal electroretinography.

Kretschmann U, Seeliger M, Ruether K, Usui T, Zrenner E. Kretschmann U, et al. Among authors: zrenner e. Vision Res. 1998 Dec;38(23):3817-28. doi: 10.1016/s0042-6989(98)00071-6. Vision Res. 1998. PMID: 9893810 Free article.

6

L- and M-cone driven ERGs are differently altered in Best's macular dystrophy.

Scholl HP, Kremers J, Apfelstedt-Sylla E, Zrenner E. Scholl HP, et al. Among authors: zrenner e. Vision Res. 2000;40(22):3159-68. doi: 10.1016/s0042-6989(00)00160-7. Vision Res. 2000. PMID: 10996618 Free article.

7

Rod and cone function in patients with KCNV2 retinopathy.

Zobor D, Kohl S, Wissinger B, Zrenner E, Jägle H. Zobor D, et al. Among authors: zrenner e. PLoS One. 2012;7(10):e46762. doi: 10.1371/journal.pone.0046762. Epub 2012 Oct 15. PLoS One. 2012. PMID: 23077521 Free PMC article.

8

Subretinal Visual Implant Alpha IMS--Clinical trial interim report.

Stingl K, Bartz-Schmidt KU, Besch D, Chee CK, Cottriall CL, Gekeler F, Groppe M, Jackson TL, MacLaren RE, Koitschev A, Kusnyerik A, Neffendorf J, Nemeth J, Naeem MA, Peters T, Ramsden JD, Sachs H, Simpson A, Singh MS, Wilhelm B, Wong D, Zrenner E. Stingl K, et al. Among authors: zrenner e. Vision Res. 2015 Jun;111(Pt B):149-60. doi: 10.1016/j.visres.2015.03.001. Epub 2015 Mar 23. Vision Res. 2015. PMID: 25812924 Free article. Clinical Trial.

9

Prevention and therapy in hereditary retinal degenerations.

Besch D, Zrenner E. Besch D, et al. Among authors: zrenner e. Doc Ophthalmol. 2003 Jan;106(1):31-5. doi: 10.1023/a:1022427813898. Doc Ophthalmol. 2003. PMID: 12675483 Review.

10

Progressive cone dystrophy with deutan genotype and phenotype.

Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H. Scholl HP, et al. Among authors: zrenner e. Graefes Arch Clin Exp Ophthalmol. 2006 Feb;244(2):183-91. doi: 10.1007/s00417-005-0022-7. Epub 2005 Aug 5. Graefes Arch Clin Exp Ophthalmol. 2006. PMID: 16082559

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