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  5. Arnim, Bettina von [Composer]; Lang, Josephine [Composer]; Egloffstein, Caroline von [Composer]; Kinkel, Johanna [Composer]; Schumann, Clara [Composer]; Anna Amalia Sachsen-Weimar-Eisenach, Herzogin [Composer]; Schröter, Corona [Composer]; Mertens-Schaaffhausen, Sibylle [Composer]; Droste-Hülshoff, Annette von [Composer]; Liebmann, Helene [Composer]; Reichardt, Louise [Composer]; Müller, Elise [Composer]; Bürde, Jeannette [Composer]; Hensel, Fanny [Composer] ; Lemke, Ann Willison [Editor]

    Von Goethe inspiriert : Lieder von Komponistinnen des 18. und 19. Jahrhunderts = Inspired by Goethe

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    Kassel: Furore-Verl., 1999

    Published in: Furore-Edition ; 630

  7. Reif-Leonhard, Christine; Lemke, Dorothea; Holz, Franziska; Ahrens, Kira F.; Fehr, Christoph; Steffens, Markus; Grube, Michael; Freitag, Christine M.; Kölzer, Sarah C.; Schlitt, Sabine; Gebhardt, Rebekka; Gädeke, Theresa; Schmidt, Helga; Gerlach, Ferdinand M.; Wolff, Kira; Stäblein, Michael; Hauschild, Nora; Beig, Inga; Wagner, Louisa; Müller, Juliane; Verhoff, Marcel A.; Schlang, Christiane; Reif, Andreas

    Changes in the pattern of suicides and suicide attempt admissions in relation to the COVID-19 pandemic

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    Springer Science and Business Media LLC, 2023

    Published in: European Archives of Psychiatry and Clinical Neuroscience, 273 (2023) 2, Seite 357-365

  8. Senderek, Jan; Bergmann, Carsten; Stendel, Claudia; Kirfel, Jutta; Verpoorten, Nathalie; De Jonghe, Peter; Timmerman, Vincent; Chrast, Roman; Verheijen, Mark H.G.; Lemke, Greg; Battaloglu, Esra; Parman, Yesim; Erdem, Sevim; Tan, Ersin; Topaloglu, Haluk; Hahn, Andreas; Müller-Felber, Wolfgang; Rizzuto, Nicolò; Fabrizi, Gian Maria; Stuhrmann, Manfred; Rudnik-Schöneborn, Sabine; Züchner, Stephan; Michael Schröder, J.; Buchheim, Eckhard; [...]

    Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

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    Elsevier BV, 2003

    Published in: The American Journal of Human Genetics, 73 (2003) 5, Seite 1106-1119

  9. Johannesen, Katrine M; Liu, Yuanyuan; Koko, Mahmoud; Gjerulfsen, Cathrine E; Sonnenberg, Lukas; Schubert, Julian; Fenger, Christina D; Eltokhi, Ahmed; Rannap, Maert; Koch, Nils A; Lauxmann, Stephan; Krüger, Johanna; Kegele, Josua; Canafoglia, Laura; Franceschetti, Silvana; Mayer, Thomas; Rebstock, Johannes; Zacher, Pia; Ruf, Susanne; Alber, Michael; Sterbova, Katalin; Lassuthová, Petra; Vlckova, Marketa; Lemke, Johannes R; [...]

    Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

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    Oxford University Press (OUP), 2022

    Published in: Brain, 145 (2022) 9, Seite 2991-3009

  10. Schmidt, Axel; Danyel, Magdalena; Grundmann, Kathrin; Brunet, Theresa; Klinkhammer, Hannah; Hsieh, Tzung-Chien; Engels, Hartmut; Peters, Sophia; Knaus, Alexej; Moosa, Shahida; Averdunk, Luisa; Boschann, Felix; Sczakiel, Henrike Lisa; Schwartzmann, Sarina; Mensah, Martin Atta; Pantel, Jean Tori; Holtgrewe, Manuel; Bösch, Annemarie; Weiß, Claudia; Weinhold, Natalie; Suter, Aude-Annick; Stoltenburg, Corinna; Neugebauer, Julia; Kallinich, Tillmann; [...]

    Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

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    Springer Science and Business Media LLC, 2024

    Published in: Nature Genetics (2024)