AAAAAA
Results: 1-25/62
Authors:
Pesch, K
Tomiuk, J
Broghammer, M
Zrenner, E
Apfelstedt-Sylla, E
Jacobi, FK
Wissinger, B
Pusch, CM
Citation: K. Pesch et al., Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders, INT J MOL M, 8(1), 2001, pp. 53-58
Authors:
Seeliger, MW
Grimm, C
Stahlberg, F
Friedburg, C
Jaissle, G
Zrenner, E
Guo, H
Reme, CE
Humphries, P
Hofmann, F
Biel, M
Fariss, RN
Redmond, TM
Wenzel, A
Citation: Mw. Seeliger et al., New views on RPE65 deficiency: the rod system is the source of vision in amouse model of Leber congenital amaurosis, NAT GENET, 29(1), 2001, pp. 70-74
Authors:
Pesch, UEA
Leo-Kottler, B
Mayor, S
Jurklies, B
Kellner, U
Apfelstedt-Sylla, E
Zrenner, E
Alexander, C
Wissinger, B
Citation: Uea. Pesch et al., OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance, HUM MOL GEN, 10(13), 2001, pp. 1359-1368
Authors:
Rejdak, R
Zarnowski, T
Turski, WA
Okuno, E
Kocki, T
Zagorski, Z
Kohler, K
Guenther, E
Zrenner, E
Citation: R. Rejdak et al., Presence of kynurenic acid and kynurenine aminotransferases in the inner retina, NEUROREPORT, 12(17), 2001, pp. 3675-3678
Authors:
Zrenner, E
Ruther, K
Citation: E. Zrenner et K. Ruther, Dosage of vitamin-A derivatives in hereditary retinal degeneration. Current recommendations, OPHTHALMOLO, 98(6), 2001, pp. 526-528
Authors:
Zrenner, E
Gekeler, F
Gabel, VP
Graf, HG
Graf, M
Guenther, E
Haemmerle, H
Hoefflinger, B
Kobuch, K
Kohler, K
Nisch, W
Sachs, H
Schlosshauer, B
Schubert, M
Schwahn, H
Stelzle, M
Stett, A
Troeger, B
Weiss, S
Citation: E. Zrenner et al., Subretinal microphotodiode arrays to replace degenerated photoreceptors?, OPHTHALMOLO, 98(4), 2001, pp. 357-363
Authors:
Kohler, K
Hartmann, JA
Werts, D
Zrenner, E
Citation: K. Kohler et al., Retinal degeneration and biocompatibility of subretinal implants: a histological analysis, OPHTHALMOLO, 98(4), 2001, pp. 364-368
Authors:
Eckhorn, R
Stett, A
Schanze, T
Gekeler, F
Schwahn, H
Zrenner, E
Wilms, M
Eger, M
Hesse, L
Citation: R. Eckhorn et al., Physiological testing of function of retinal implants with animal models, OPHTHALMOLO, 98(4), 2001, pp. 369-375
Authors:
Jurklies, B
Weismann, M
Kellner, U
Zrenner, E
Bornfeld, N
Citation: B. Jurklies et al., Clinical findings in autosomal recessive enhanced S-cone sensitivity syndrome, OPHTHALMOLO, 98(3), 2001, pp. 285-293
Authors:
Scholl, HPN
Langrova, H
Weber, BHF
Zrenner, E
Apfelstedt-Sylla, E
Citation: Hpn. Scholl et al., Clinical electrophysiology of two rod pathways: normative values and clinical application, GR ARCH CL, 239(2), 2001, pp. 71-80
Authors:
Erb, C
Voelker, W
Adler, M
Wohlrab, M
Zrenner, E
Citation: C. Erb et al., Color-vision disturbances in patients with coronary artery disease, COL RES APP, 26, 2001, pp. S288-S291
Authors:
Rizzo, JF
Wyatt, J
Humayun, M
de Juan, E
Liu, WT
Chow, A
Eckmiller, R
Zrenner, E
Yagi, T
Abrams, G
Citation: Jf. Rizzo et al., Retinal prosthesis - An encouraging first decade with major challenges ahead, OPHTHALMOL, 108(1), 2001, pp. 13-14
Authors:
Wenzel, A
Grimm, C
Seeliger, MW
Jaissle, G
Hafezi, F
Kretschmer, R
Zrenner, E
Reme, CE
Citation: A. Wenzel et al., Prevention of photoreceptor apoptosis by activation of the glucocorticoid receptor, INV OPHTH V, 42(7), 2001, pp. 1653-1659
Authors:
Jacobi, FK
Leo-Kottler, B
Mittelviefhaus, K
Zrenner, E
Meyer, J
Pusch, CM
Wissinger, B
Citation: Fk. Jacobi et al., Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy, INV OPHTH V, 42(6), 2001, pp. 1208-1214
Authors:
Jaissle, GB
May, CA
Reinhard, J
Kohler, K
Fauser, S
Lutjen-Drecoll, E
Zrenner, E
Seeliger, MW
Citation: Gb. Jaissle et al., Evaluation of the rhodopsin knockout mouse as a model of pure cone function, INV OPHTH V, 42(2), 2001, pp. 506-513
Authors:
Seeliger, MW
Zrenner, E
Apfelstedt-Sylla, E
Jaissle, GB
Citation: Mw. Seeliger et al., Identification of Usher syndrome subtypes by ERG implicit time, INV OPHTH V, 42(12), 2001, pp. 3066-3071
Authors:
Scholl, HPN
Langrova, H
Pusch, CM
Wissinger, B
Zrenner, E
Apfelstedt-Sylla, E
Citation: Hpn. Scholl et al., Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene, INV OPHTH V, 42(11), 2001, pp. 2728-2736
Authors:
Wilhelm, B
Ludtke, H
Peters, T
Schmid, R
Wilhelm, H
Zrenner, E
Citation: B. Wilhelm et al., Automated swinging flashlight test in patients with optic nerve disorders, KLIN MONATS, 218(1), 2001, pp. 21-25
Authors:
Wissinger, B
Gamer, D
Jagle, H
Giorda, R
Marx, T
Mayer, S
Tippmann, S
Broghammer, M
Jurklies, B
Rosenberg, T
Jacobson, SG
Sener, EC
Tatlipinar, S
Hoyng, CB
Castellan, C
Bitoun, P
Andreasson, S
Rudolph, G
Kellner, U
Lorenz, B
Wolff, G
Verellen-Dumoulin, C
Schwartz, M
Cremers, FPM
Apfelstedt-ylla, E
Zrenner, E
Salati, R
Sharpe, LT
Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
Authors:
Kohl, S
Baumann, B
Broghammer, M
Jagle, H
Sieving, P
Kellner, U
Spegal, R
Anastasi, M
Zrenner, E
Sharpe, LT
Wissinger, B
Citation: S. Kohl et al., Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21, HUM MOL GEN, 9(14), 2000, pp. 2107-2116
Authors:
Konig, HH
Barry, JC
Leidl, R
Zrenner, E
Citation: Hh. Konig et al., Test-effectiveness of orthoptic mass screening in kindergarten for early detection of visual development disorders, GESUNDHEITS, 62(4), 2000, pp. 196-206
Authors:
Erb, C
Teistler, F
Kohler, K
Guenther, E
Zrenner, E
Thiel, HJ
Citation: C. Erb et al., Evaluation of the applanation tonometer ProTon in rabbits, OPHTHALMOLO, 97(11), 2000, pp. 788-791
Authors:
Besch, D
Wissinger, B
Zrenner, E
Leo-Kottler, B
Citation: D. Besch et al., A case of liver optic neuropathy with a new point mutation in the cytochrome b gene, OPHTHALMOLO, 97(1), 2000, pp. 27-32
Authors:
Jacobi, FK
Broghammer, M
Pesch, K
Zrenner, E
Berger, W
Meindl, A
Pusch, CM
Citation: Fk. Jacobi et al., Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1, HUM GENET, 107(1), 2000, pp. 89-91
Authors:
Wilhelm, H
Neitzel, J
Wilhelm, B
Beuel, S
Ludtke, H
Kretschmann, U
Zrenner, E
Citation: H. Wilhelm et al., Pupil perimetry using M-sequence stimulation technique, INV OPHTH V, 41(5), 2000, pp. 1229-1238