Resultados de procura - Barbara Käsmann‐Kellner

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  1. 1
    Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4

    Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4 por Uta Rundshagen, Christine Zühlke, Sven Opitz, E. Schwinger, Barbara Käsmann‐Kellner

    Publicado 2004
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  2. 2
    Biomechanical profile of the cornea in primary congenital glaucoma

    Biomechanical profile of the cornea in primary congenital glaucoma por Zisis Gatzioufas, Georgios Labiris, Oliver Stachs, Marine Hovakimyan, A Schnaidt, Arne Viestenz, Barbara Käsmann‐Kellner, Berthold Seitz

    Publicado 2012
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  3. 3
    PAX6 Mutational Status Determines Aniridia-Associated Keratopathy Phenotype

    PAX6 Mutational Status Determines Aniridia-Associated Keratopathy Phenotype por Neil Lagali, Bogumił Wowra, Fabian N. Fries, Lorenz Latta, Kayed Moslemani, Tor Paaske Utheim, Edward Wylęgała, Berthold Seitz, Barbara Käsmann‐Kellner

    Publicado 2019
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  4. 4
    Early phenotypic features of aniridia-associated keratopathy and association with PAX6 coding mutations

    Early phenotypic features of aniridia-associated keratopathy and association with PAX6 coding mutations por Neil Lagali, Bogumił Wowra, Fabian N. Fries, Lorenz Latta, Kayed Moslemani, Tor Paaske Utheim, Edward Wylęgała, Berthold Seitz, Barbara Käsmann‐Kellner

    Publicado 2019
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  5. 5
    Systemic Diseases in Patients with Congenital Aniridia: A Report from the Homburg Registry for Congenital Aniridia

    Systemic Diseases in Patients with Congenital Aniridia: A Report from the Homburg Registry for Congenital Aniridia por Jessica Obst, Fabian N. Fries, Maryam Amini, Annamária Náray, Cristian Munteanu, Tanja Stachon, Shweta Suiwal, Neil Lagali, Berthold Seitz, Barbara Käsmann‐Kellner, Nóra Szentmáry

    Publicado 2025
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  6. 6
    Abnormal neovascular and proliferative conjunctival phenotype in limbal stem cell deficiency is associated with altered microRNA and gene expression modulated by PAX6 mutational status in congenital aniridia

    Abnormal neovascular and proliferative conjunctival phenotype in limbal stem cell deficiency is associated with altered microRNA and gene expression modulated by PAX6 mutational st... por Lorenz Latta, Nicole Ludwig, Lena Krammes, Tanja Stachon, Fabian N. Fries, Anthony Mukwaya, Nóra Szentmáry, Berthold Seitz, Bogumił Wowra, Mustafa Kahraman, Andreas Keller, Eckart Meese, Neil Lagali, Barbara Käsmann‐Kellner

    Publicado 2020
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