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Publications by Scholl, H P N

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Jump to: 2005 | 2002 | 2001 | 2000
Number of items: 5.

2005

Scholl, H P N, Weber, Bernhard H. F. , Nöthen, M M, Wienker, T and Holz, F G (2005) Y402H-Polymorphismus im Komplementfaktor H und altersabhängige Makuladegeneration (AMD) -- Y402H polymorphism in complement factor H and age-related macula degeneration (AMD). Der Ophthalmologe 102 (11), pp. 1029-1035. Fulltext not available.

2002

Scholl, H P N, Besch, D, Vonthein, R, Weber, Bernhard H. F. and Apfelstedt-Sylla, E (2002) Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1 (STGD1). Investigative ophthalmology and visual science 43 (4), pp. 1248-1256.

2001

Scholl, H P N, Langrova, H, Weber, Bernhard H. F. , Zrenner, E and Apfelstedt-Sylla, E (2001) Clinical electrophysiology of two rod pathways: normative values and clinical application. Graefe's Archive for Clinical and Experimental Ophthalmology 239 (2), pp. 71-80. Fulltext not available.

Scholl, H P N, Kremers, J, Vonthein, R, White, K and Weber, Bernhard H. F. (2001) L- and M-Cone–Driven Electroretinograms in Stargardt’s Macular Dystrophy–Fundus Flavimaculatus. Investigative ophthalmology and visual science 42, pp. 1380-1389.

2000

Rivera, A, White, K, Stöhr, H, Steiner, K, Hemmrich, N, Grimm, T, Jurklies, B, Lorenz, B, Scholl, H P N, Apfelstedt-Sylla, E and Weber, Bernhard H. F. (2000) A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration. The American Journal of Human Genetics 67 (4), pp. 800-813. Fulltext not available.

This list was generated on Tue Feb 25 20:27:15 2020 CET.
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