Klaus Rohrschneider
Klaus Rohrschneider
Leiter Ophthalmologische Rehabilitation und seltene Augenerkrankungen, Universitätsaugenklinik
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Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis
AI den Hollander, RK Koenekoop, S Yzer, I Lopez, ML Arends, ...
The American Journal of Human Genetics 79 (3), 556-561, 2006
Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR
FPM Cremers, DJR van de Pol, M van Driel, AI den Hollander, ...
Human molecular genetics 7 (3), 355-362, 1998
Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers
FE Kruse, K Rohrschneider, HE Völcker
Ophthalmology 106 (8), 1504-1511, 1999
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene
AI den Hollander, JR Heckenlively, LI van den Born, YJM de Kok, ...
The American Journal of Human Genetics 69 (1), 198-203, 2001
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy
A Maugeri, BJ Klevering, K Rohrschneider, A Blankenagel, HG Brunner, ...
The American Journal of Human Genetics 67 (4), 960-966, 2000
Reproducibility of the optic nerve head topography with a new laser tomographic scanning device
K Rohrschneider, ROW Burk, FE Kruse, HE Völcker
Ophthalmology 101 (6), 1044-1049, 1994
The 2588G→ C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with …
A Maugeri, MA van Driel, DJR van de Pol, BJ Klevering, FJJ van Haren, ...
The American Journal of Human Genetics 64 (4), 1024-1035, 1999
Cryopreserved human amniotic membrane for ocular surface reconstruction
FE Kruse, AM Joussen, K Rohrschneider, L You, B Sinn, J Baumann, ...
Graefe's archive for clinical and experimental ophthalmology 238, 68-75, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular …
F Krämer, K White, D Pauleikhoff, A Gehrig, L Passmore, A Rivera, ...
European Journal of Human Genetics 8 (4), 286-292, 2000
Use of fundus perimetry (microperimetry) to quantify macular sensitivity
K Rohrschneider, S Bültmann, C Springer
Progress in retinal and eye research 27 (5), 536-548, 2008
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
LM Astuto, JM Bork, MD Weston, JW Askew, RR Fields, DJ Orten, ...
The American Journal of Human Genetics 71 (2), 262-275, 2002
Thalidomide inhibits corneal angiogenesis induced by vascular endothelial growth factor
FE Kruse, AM Joussen, K Rohrschneider, MD Becker, HE Völcker
Graefe's archive for clinical and experimental ophthalmology 236, 461-466, 1998
Fundus autofluorescence and fundus perimetry in the junctional zone of geographic atrophy in patients with age-related macular degeneration
S Schmitz-Valckenberg, S Bültmann, J Dreyhaupt, A Bindewald, ...
Investigative ophthalmology & visual science 45 (12), 4470-4476, 2004
Microperimetry—comparison between the micro perimeter 1 and scanning laser ophthalmoscope—fundus perimetry
K Rohrschneider, C Springer, S Bültmann, HE Vö
American journal of ophthalmology 139 (1), 125-134, 2005
Autologous translocation of the choroid and retinal pigment epithelium in age-related macular degeneration
AM Joussen, FMA Heussen, S Joeres, H Llacer, B Prinz, K Rohrschneider, ...
American journal of ophthalmology 142 (1), 17-30. e8, 2006
Determination of the location of the fovea on the fundus
K Rohrschneider
Investigative ophthalmology & visual science 45 (9), 3257-3258, 2004
Fundus perimetry with the Micro Perimeter 1 in normal individuals: comparison with conventional threshold perimetry
C Springer, S Bültmann, HE Völcker, K Rohrschneider
Ophthalmology 112 (5), 848-854, 2005
A novel nonsense mutation in CEP290 induces exon skipping and leads to a relatively mild retinal phenotype
KW Littink, JWR Pott, RWJ Collin, HY Kroes, JBGM Verheij, EAW Blokland, ...
Investigative ophthalmology & visual science 51 (7), 3646-3652, 2010
IQCB1 mutations in patients with leber congenital amaurosis
A Estrada-Cuzcano, RK Koenekoop, F Coppieters, S Kohl, I Lopez, ...
Investigative ophthalmology & visual science 52 (2), 834-839, 2011
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa
BJ Klevering, S Yzer, K Rohrschneider, M Zonneveld, R Allikmets, L Born, ...
European journal of human genetics 12 (12), 1024-1032, 2004
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