Research for Rare - Forschung für seltene Erkrankungen

Publikationen der Forschungsverbünde

Paper of the quarter

7. Oktober 2026 (Treat-ION)
KCNA2-Associated Hereditary Spastic Paraplegia: Clinical Characteristics and Rationale for Targeted Treatment

Mov Disord. 2026 Oct 7. >>Pubmed-Link<<  

Christian M Boßelmann, Martin Vyhnalek, Zuzana Blichova, Ludmila Novotna, Anna Uhrova Meszarosova, Petra Havránková, Elena Kuster, Robert J Lauerer, Ulrike B S Hedrich, Hang Lyu, Mayke Oosterloo, Michael Alber, Ludger Schöls, Karen Müller-Schlüter, Almut Turid Bischoff, Thomas Klopstock, Georgios Koutsis, Georgia Karadima, Stephanie Efthymiou, Henry Houlden, Ainara Salazar-Villacorta, Colin A Ellis, Anna Scheper, Dieter Gläser, Tobias B Haack, Matias Wagner, Michael Zech, Konrad Platzer, Pasquale Striano, Steffen Syrbe, Rebecca Schüle, Holger Lerche
network cooperation: Treat-ION, TreatHSP.net, mitoNET

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25. September 2026 (CONNECT-GENERATE)
Diagnosing autoimmune encephalitis in psychiatry: clinical recommendations and unresolved challenges from the GENERATE network

Mol Psychiatry. 2026 Sep 25. >>Nature-Link<<

Dominique Endres, Katharina von Zedtwitz, Ludger Tebartz van Elst, Katharina Domschke, Judith Weiser, Arnim J Gaebler, Thomas Frodl, Elias Wagner, Iris Jäger, Alkomiet Hasan, Josef Priller, Cora Schefft, Paul J Wirsching, Sibylle Haußleiter, Georg Juckel, Philipp Müller, David H V Vogel, Alexandra Philipsen, Timo J Faustmann, Daniel Kamp, Leonhard Schilbach, Dag Scherfeld, Milenko Kujovic, Eva Meisenzahl, Stefanie Fischer, Jonathan Repple, Udo Dannlowski, Niels Hansen, Karl Bechter, Oliver Tüscher, Heiko Paland, Daniel Luedecke, Hannah B Maier, Margarete Mattern, Michael Kluge, Alexandra Neyazi, Johann Steiner, Sebastian Walther, Ilya Ayzenberg, Manuel A Friese, Tania Kümpfel, Sven G Meuth, Kevin Rostasy, Simone C Tauber, Franziska S Thaler, Klaus-Peter Wandinger, Brigitte Wildemann, Carsten Finke, Jan Lewerenz, Christian Geis, Nico Melzer, Harald Prüss, Frank Leypoldt

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1. September 2026 (MitoNet)
Mitochondrial diabetes mellitus: real world insights from the GENOMIT registry-a multinational, longitudinal cohort study

EBioMedicine. 2026 Sep 1. >>Pubmed-Link<<  

Luisa Semmler, Boriana Büchner, Cornelia Kornblum, Marcus Deschauer, Saskia Wortmann, Chiara La Morgia, Serenella Servidei, Peter Freisinger, Alexander Mensch, Markus Schuelke, Holger Prokisch, Michelangelo Mancuso, Costanza Lamperti, Thomas Klopstock; GENOMIT study group

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