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Results:
1-17
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Results: 17
Authors:
Sadowski, B
Kriegbaum, C
Apfelstedt-Sylla, E
Citation: B. Sadowski et al., Tamoxifen side effects, age-related macular degeneration (AMD) or cancer associated retinopathy (CAR)?, EUR J OPTHA, 11(3), 2001, pp. 309-312
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:
Pusch, CM
Maurer, J
Ramser, J
Tomiuk, J
Achatz, H
Pesch, K
Lichtner, P
Apfelstedt-Sylla, E
Jacobi, FK
Berger, W
Meindl, A
Wissinger, B
Citation: Cm. Pusch et al., Complete form of X-linked congenital stationary night blindness: Refined mapping and evidence of genetic homogeneity, INT J MOL M, 7(2), 2001, pp. 155-161
Authors:
Thompson, DA
Li, Y
McHenry, CL
Carlson, TJ
Ding, X
Sieving, PA
Apfelstedt-Sylla, E
Gal, A
Citation: Da. Thompson et al., Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy, NAT GENET, 28(2), 2001, pp. 123-124
Authors:
Zwaenepoel, I
Verpy, E
Blanchard, S
Meins, M
Apfelstedt-Sylla, E
Gal, A
Petit, C
Citation: I. Zwaenepoel et al., Identification of three novel mutations in the USH1C gene and detection ofthirty-one polymorphisms used for haplotype analysis, HUM MUTAT, 17(1), 2001, pp. 34-41
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:
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:
Jagle, H
Kohl, S
Apfelstedt-Sylla, E
Wissinger, B
Sharpe, LT
Citation: H. Jagle et al., Manifestations of rod monochromacy, COL RES APP, 26, 2001, pp. S96-S99
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:
Gal, A
Li, Y
Thompson, DA
Weir, J
Orth, U
Jacobson, SG
Apfelstedt-Sylla, E
Vollrath, D
Citation: A. Gal et al., Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa, NAT GENET, 26(3), 2000, pp. 270-271
Authors:
Thompson, DA
Gyurus, P
Fleischer, LL
Bingham, EL
McHenry, CL
Apfelstedt-Sylla, E
Zrenner, E
Lorenz, B
Richards, JE
Jacobson, SG
Sieving, PA
Gal, A
Citation: Da. Thompson et al., Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration, INV OPHTH V, 41(13), 2000, pp. 4293-4299
Authors:
Scholl, HPN
Kremers, J
Apfelstedt-Sylla, E
Zrenner, E
Citation: Hpn. Scholl et al., L- and M-cone driven ERGs are differently altered in Best's macular dystrophy, VISION RES, 40(22), 2000, pp. 3159-3168
Authors:
Rivera, A
White, K
Stohr, H
Steiner, K
Hemmrich, N
Grimm, T
Jurklies, B
Lorenz, B
Scholl, HPN
Apfelstedt-Sylla, E
Weber, BHF
Citation: A. Rivera et al., A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration, AM J HU GEN, 67(4), 2000, pp. 800-813
Authors:
Janecke, AR
Meins, M
Sadeghi, M
Grundmann, K
Apfelstedt-Sylla, E
Zrenner, E
Rosenberg, T
Gal, A
Citation: Ar. Janecke et al., Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome typeI: Confirmation of genetic heterogeneity, HUM MUTAT, 13(2), 1999, pp. 133-140
Authors:
Seeliger, M
Pfister, M
Gendo, K
Paasch, S
Apfelstedt-Sylla, E
Plinkert, P
Zenner, HP
Zrenner, E
Citation: M. Seeliger et al., Comparative study of visual, auditory, and olfactory function in Usher syndrome, GR ARCH CL, 237(4), 1999, pp. 301-307
Authors:
Kohl, S
Giddings, I
Besch, D
Apfelstedt-Sylla, E
Zrenner, E
Wissinger, B
Citation: S. Kohl et al., The role of the peripherin/RDS gene in retinal dystrophies, ACT ANATOM, 162(2-3), 1998, pp. 75-84
Risultati:
1-17
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