Search Results - Cropp, Elke

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  1. 1
    Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations

    Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations by Renner, Agnes B, Fiebig, Britta S, Weber, Bernhard H.F, Wissinger, Bernd, Andreasson, Sten, Gal, Andreas, Cropp, Elke, Kohl, Susanne, Kellner, Ulrich

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  2. 2
    ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT

    ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT by Renner, Agnes B., Kellner, Ulrich, Fiebig, Britta, Cropp, Elke, Foerster, Michael H., Weber, Bernhard H. F.

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  3. 3
    Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram

    Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram by Renner, Agnes B, Kellner, Ulrich, Cropp, Elke, Foerster, Michael H

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  4. 4
    ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT: Retinal Imaging and Electrophysiology in the Assessment of Retinal Diseases

    ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT: Retinal Imaging and E... by RENNER, Agnes B, KELLNER, Ulrich, FIEBIG, Britta, CROPP, Elke, FOERSTER, Michael H, WEBER, Bernhard H. F

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