检索结果 - Käsmann‐Kellner, Barbara

Doppelbilder bei einem 60-jährigen Patienten 由 Maamri, Amine, Suffo, Shady, Käsmann-Kellner, Barbara, Seitz, Berthold

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Retinal Nerve Fibre Layer Thinning in Patients with Clinically Isolated Optic Neuritis and Early Treatment with Interferon-Beta 由 Sühs, Kurt-Wolfram, Hein, Katharina, Pehlke, Jens R., Käsmann-Kellner, Barbara, Diem, Ricarda

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Keratin 12 mRNA expression could serve as an early corneal marker for limbal explant cultures 由 Shi, Lei, Stachon, Tanja, Käsmann-Kellner, Barbara, Seitz, Berthold, Szentmáry, Nóra, Latta, Lorenz

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A Novel Likely Pathogenic Variant in the BLOC1S5 Gene Associated with Hermansky-Pudlak Syndrome Type 11 and an Overview of Human BLOC-1 Deficiencies 由 Boeckelmann, Doris, Wolter, Mira, Käsmann-Kellner, Barbara, Koehler, Udo, Schieber-Nakamura, Lea, Zieger, Barbara

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Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging 由 Schmitz, Bernd, Käsmann‐Kellner, Barbara, Schäfer, Torsten, Krick, Christoph M., Grön, Georg, Backens, Martin, Reith, Wolfgang

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Hermansky-Pudlak Syndrome: Identification of Novel Variants in the Genes HPS3, HPS5, and DTNBP1 (HPS-7) 由 Boeckelmann, Doris, Wolter, Mira, Neubauer, Katharina, Sobotta, Felix, Lenz, Antonia, Glonnegger, Hannah, Käsmann-Kellner, Barbara, Mann, Jasmin, Ehl, Stephan, Zieger, Barbara

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Similarities in DSG1 and KRT3 Downregulation through Retinoic Acid Treatment and PAX6 Knockdown Related Expression Profiles: Does PAX6 Affect RA Signaling in Limbal Epithelial Cell... 由 Latta, Lorenz, Knebel, Igor, Bleil, Constanze, Stachon, Tanja, Katiyar, Priya, Zussy, Claire, Fries, Fabian Norbert, Käsmann-Kellner, Barbara, Seitz, Berthold, Szentmáry, Nóra

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Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia 由 Lowndes, Rebecca, Molz, Barbara, Warriner, Lucy, Herbik, Anne, de Best, Pieter B., Raz, Noa, Gouws, Andre, Ahmadi, Khazar, McLean, Rebecca J., Gottlob, Irene, Kohl, Susanne, Choritz, Lars, Maguire, John, Kanowski, Martin, Käsmann-Kellner, Barbara, Wieland, Ilse, Banin, Eyal, Levin, Netta, Hoffmann, Michael B., Morland, Antony B., Baseler, Heidi A.

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Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia 由 Molz, Barbara, Herbik, Anne, Baseler, Heidi A., de Best, Pieter B., Vernon, Richard W., Raz, Noa, Gouws, Andre D., Ahmadi, Khazar, Lowndes, Rebecca, McLean, Rebecca J., Gottlob, Irene, Kohl, Susanne, Choritz, Lars, Maguire, John, Kanowski, Martin, Käsmann-Kellner, Barbara, Wieland, Ilse, Banin, Eyal, Levin, Netta, Hoffmann, Michael B., Morland, Antony B.

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Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome 由 Epting, Daniel, Senaratne, Lokuliyange D. S., Ott, Elisabeth, Holmgren, Asbjørn, Sumathipala, Dulika, Larsen, Selma M., Wallmeier, Julia, Bracht, Diana, Frikstad, Kari‐Anne M., Crowley, Suzanne, Sikiric, Alma, Barøy, Tuva, Käsmann‐Kellner, Barbara, Decker, Eva, Decker, Christian, Bachmann, Nadine, Patzke, Sebastian, Phelps, Ian G., Katsanis, Nicholas, Giles, Rachel, Schmidts, Miriam, Zucknick, Manuela, Lienkamp, Soeren S., Omran, Heymut, Davis, Erica E., Doherty, Dan, Strømme, Petter, Frengen, Eirik, Bergmann, Carsten, Misceo, Doriana

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