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Ophthalmic Genetics|June 1, 1996
Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease geneU Kellner, S Fuchs, N Bornfeld, et al.
German Journal of Ophthalmology|April 1, 1993
Variation of temporal stimulus characteristics to evaluate visual function prior to pars plana vitrectomyM H Foerster, U Kellner, A Beyer, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 2, 2004
[Molecular genetic findings in patients with congenital cone dysfunction. Mutations in the CNGA3, CNGB3, or GNAT2 genes]U Kellner, B Wissinger, S Kohl, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Refined mapping of the gene encoding the p127 kDa UV-damaged DNA-binding protein (DDB1) within 11q12-q13.1 and its exclusion in Best's vitelliform macular dystrophyH Stöhr, A Marquardt, A Rivera, et al.
German Journal of Ophthalmology|May 1, 1995
Natural course of retinal development in preterm infants without threshold retinopathyC Jandeck, U Kellner, H Helbig, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 1, 1994
[Varicella zoster virus infections of the retina in patients with and without immune suppression]H Helbig, N Bornfeld, N E Bechrakis, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 7, 2004
[Clinical diagnostic prerequisites for adult vitelliform macular dystrophy]A B Renner, H Tillack, H Kraus, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|May 26, 2001
[Vitrectomy in advanced Coats disease]L Krause, K M Kreusel, C Jandeck, et al.
Der Pathologe|September 6, 2008
[YB-1 as a potential target in cancer therapy]H Lage, P Surowiak, P S Holm
The British Journal of Ophthalmology|November 3, 1998
Electrophysiological evaluation of visual loss in Müller cell sheen dystrophyU Kellner, H Kraus, H Heimann, et al.
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