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Results: 1-9 |
Results: 9
A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I
Authors: Otterstedde, CR Spandau, U Blankenagel, A Kimberling, WJ Reisser, C
Citation: Cr. Otterstedde et al., A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I, LARYNGOSCOP, 111(1), 2001, pp. 84-86
Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene
Authors: den Hollander, AI Heckenlively, JR van den Born, LI de Kok, YJM van der Velde-Visser, SD Kellner, U Jurklies, B van Schooneveld, MJ Blankenagel, A Rohrschneider, K Wissinger, B Cruysberg, JRM Deutman, AF Brunner, HG Apfeldstedt-Sylla, E Hoyng, CB Cremers, FPM
Citation: Ai. Den Hollander et al., Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene, AM J HU GEN, 69(1), 2001, pp. 198-203
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 degeneration
Authors: Kramer, F White, K Pauleikhoff, D Gehrig, A Passmore, L Rivera, A Rudolph, G Kellner, U Andrassi, M Lorenz, B Rohrschneider, K Blankenagel, A Jurklies, B Schilling, H Schutt, F Holz, FG Weber, BHF
Citation: F. Kramer et al., 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 degeneration, EUR J HUM G, 8(4), 2000, pp. 286-292
Legal reforms in Russia: Visible steps, obvious gaps, and an invisible hand?
Authors: Blankenagel, A
Citation: A. Blankenagel, Legal reforms in Russia: Visible steps, obvious gaps, and an invisible hand?, J I THEOR E, 156(1), 2000, pp. 99-119
Use of a new night vision enhancement device (DAVIS)
Authors: Rohrschneider, K Spandau, U Wechsler, S Blankenagel, A
Citation: K. Rohrschneider et al., Use of a new night vision enhancement device (DAVIS), KLIN MONATS, 217(2), 2000, pp. 88-93
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy
Authors: Maugeri, A Klevering, BJ Rohrschneider, K Blankenagel, A Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM
Citation: A. Maugeri et al., Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy, AM J HU GEN, 67(4), 2000, pp. 960-966
Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg
Authors: Rohrschneider, K Bruder, I Blankenagel, A
Citation: K. Rohrschneider et al., Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg, OPHTHALMOLO, 96(9), 1999, pp. 611-616
The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease
Authors: Maugeri, A van Driel, MA van de Pol, DJR Klevering, BJ van Haren, FJJ Tijmes, N Bergen, AAB Rohrschneider, K Blankenagel, A Pinckers, AJLG Dahl, N Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM
Citation: A. Maugeri et al., The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease, AM J HU GEN, 64(4), 1999, pp. 1024-1035
Analysis of aniridia patients for mutations in the PAX6 gene
Authors: Wolf, M Zabel, B Lorenz, B Blankenagel, A Ghorbani, MB Schwenn, O Wildhardt, G
Citation: M. Wolf et al., Analysis of aniridia patients for mutations in the PAX6 gene, OPHTHALMOLO, 95(12), 1998, pp. 828-830
Risultati: 1-9 |