Výsledky vyhledávání - Moritz Tacke

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  1. 1
    Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center

    Impact on Clinical Decision Making of Next-Generation Sequencing in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center Autor Hannes Hoelz, Christian Herdl, Lucia Gerstl, Moritz Tacke, Katharina Vill, Celina von Stuelpnagel, Imma Rost, Konstanze Hoertnagel, Angela Abicht, Sebastian Hollizeck, Line H.G. Larsen, Ingo Borggraefe

    Vydáno 2019
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  2. 2
    First detected geographical cluster of BoDV-1 encephalitis from same small village in two children: therapeutic considerations and epidemiological implications

    First detected geographical cluster of BoDV-1 encephalitis from same small village in two children: therapeutic considerations and epidemiological implications Autor Leonie Grosse, Victoria Lieftüchter, Yannik Vollmuth, Florian Hoffmann, Martin Olivieri, Karl Reiter, Moritz Tacke, Florian Heinen, Ingo Borggraefe, Andreas Osterman, Maria Forstner, Johannes Hübner, Ulrich von Both, Lena Birzele, Meino Rohlfs, Adrian Schomburg, Merle M. Böhmer, Viktoria Ruf, Dániel Cadar, Birgit Muntau, Kirsten Pörtner, Dennis Tappe

    Vydáno 2023
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  3. 3
    Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy

    Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy Autor Matias Wagner, Géza Berecki, Walid Fazeli, Claudia Nußbaum, Andreas W. Flemmer, Silvana Frizzo, F. Heer, Florian Heinen, Robert Horton, Henry Jacotin, WILLIAM G. MOTEL, Brian D. Spar, Christoph Klein, Corinna Siegel, Christoph Hübener, Sophia Stöcklein, Marco Paolini, Martin Staudt, Moritz Tacke, Markus Wolff, Steven Petrou, Marcio Souza, Ingo Borggraefe

    Vydáno 2025
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  4. 4
    5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2

    5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2 Autor Katharina Vill, Moritz Tacke, Anna König, Matthias Baumann, Manuela Baumgärtner, Robert Steinbach, Guenther Bernert, Astrid Blaschek, Marcus Deschauer, Marina Flotats‐Bastardas, Johannes Friese, Susanne Goldbach, Martin Groß, René Günther, Andreas Hahn, Tim Hagenacker, Erwin Hauser, Veronka Horber, Sabine Illsinger, Jessika Johannsen, Christoph Kamm, Jan Christoph Koch, H. Koelbel, Cornelia Koehler, Kirsten Kolzter, Hanns Lochmüller, Albert C. Ludolph, Alexander Mensch, Gerd Meyer zu Hoerste, Monika Mueller, Wolfgang Mueller‐Felber, Christoph Neuwirth, Susanne Petri, Kristina Probst-Schendzielorz, Manuel Pühringer, Robert Steinbach, Ulrike Schara‐Schmidt, Mareike Schimmel, Bertold Schrank, Oliver Schwartz, Kurt Schlachter, Annette Schwerin-Nagel, Gudrun Schreiber, Martin Smitka, Raffi Topakian, Regina Trollmann, Matthias Tuerk, Manuela Theophil, Christian Rauscher, Mathias Vorgerd, Maggie C. Walter, Markus Weiler, Claudia Weiß, Ekkehard Wilichowski, Claudia D. Wurster, Gilbert Wunderlich, Daniel Zeller, Andreas Ziegler, Janbernd Kirschner, Astrid Pechmann

    Vydáno 2024
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