Response to: ‘JAK inhibition in STING-associated interferonopathy’ by Crow et al von Tüngler, Victoria, König, Nadja, Günther, Claudia, Engel, Kerstin, Fiehn, Christoph, Smitka, Martin, von der Hagen, Maja, Berner, Reinhard, Lee-Kirsch, Min Ae

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Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis von Hölzer, Hans Thomas, Boschann, Felix, Hennermann, Julia B., Hahn, Gabriele, Hermann, Andreas, von der Hagen, Maja, Tüngler, Victoria

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Troponin T is elevated in a relevant proportion of patients with 5q-associated spinal muscular atrophy von Lapp, Hanna Sophie, Freigang, Maren, Friese, Johannes, Bernsen, Sarah, Tüngler, Victoria, von der Hagen, Maja, Weydt, Patrick, Günther, René

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Serum neurofilament light chain in pediatric spinal muscular atrophy patients and healthy children von Nitz, Elisa, Smitka, Martin, Schallner, Jens, Akgün, Katja, Ziemssen, Tjalf, Hagen, Maja, Tüngler, Victoria

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Single-stranded nucleic acids promote SAMHD1 complex formation von Tüngler, Victoria, Staroske, Wolfgang, Kind, Barbara, Dobrick, Manuela, Kretschmer, Stefanie, Schmidt, Franziska, Krug, Claudia, Lorenz, Mike, Chara, Osvaldo, Schwille, Petra, Lee-Kirsch, Min Ae

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Naturally Occurring Genetic Variants of Human Caspase-1 Differ Considerably in Structure and the Ability to Activate Interleukin-1[beta] von Luksch, Hella, Romanowski, Michael J, Chara, Osvaldo, Tungler, Victoria, Caffarena, Ernesto R, Heymann, Michael C, Lohse, Peter, Aksentijevich, Ivona, Remmers, Elaine F, Flecks, Silvana, Quoos, Nadine, Gramatte, Johannes, Petzold, Cathleen, Hofmann, Sigrun R, Winkler, Stefan, Pessler, Frank, Kallinich, Tilmann, Ganser, Gerd, Nimtz-Talaska, Antje, Baumann, Ulrich, Runde, Volker, Grimbacher, Bodo, Birmelin, Jennifer, Gahr, Manfred, Roesler, Joachim, Rosen-Wolff, Angela

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Management of external small bowel fistulae: Challenges and controversies confronting the general surgeon von Wainstein, Daniel E, Tüngler, Victoria, Ravazzola, Constanza, Chara, Osvaldo

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Defective removal of ribonucleotides from DNA promotes systemic autoimmunity von Günther, Claudia, Kind, Barbara, Reijns, Martin A M, Berndt, Nicole, Martinez-Bueno, Manuel, Wolf, Christine, Tüngler, Victoria, Chara, Osvaldo, Lee, Young Ae, Hübner, Norbert, Bicknell, Louise, Blum, Sophia, Krug, Claudia, Schmidt, Franziska, Kretschmer, Stefanie, Koss, Sarah, Astell, Katy R, Ramantani, Georgia, Bauerfeind, Anja, Morris, David L, Cunninghame Graham, Deborah S, Bubeck, Doryen, Leitch, Andrea, Ralston, Stuart H, Blackburn, Elizabeth A, Gahr, Manfred, Witte, Torsten, Vyse, Timothy J, Melchers, Inga, Mangold, Elisabeth, Nöthen, Markus M, Aringer, Martin, Kuhn, Annegret, Lüthke, Kirsten, Unger, Leonore, Bley, Annette, Lorenzi, Alice, Isaacs, John D, Alexopoulou, Dimitra, Conrad, Karsten, Dahl, Andreas, Roers, Axel, Alarcon-Riquelme, Marta E, Jackson, Andrew P, Lee-Kirsch, Min Ae

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Neurofilament light protein as a biomarker for spinal muscular atrophy: a review and reference ranges von Bayoumy, Sherif, Verberk, Inge M.W., Vermunt, Lisa, Willemse, Eline, den Dulk, Ben, van der Ploeg, Ans T., Pajkrt, Dasja, Nitz, Elisa, van den Hout, Johanna M.P., van der Post, Julie, Wolf, Nicole I., Beerepoot, Shanice, Groen, Ewout J.N., Tüngler, Victoria, Teunissen, Charlotte E.

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Neurofilament light protein as a biomarker for spinal muscular atrophy: A review and reference ranges von Bayoumy, Sherif, Verberk, Inge M.W, Vermunt, Lisa, Willemse, Eline, Den Dulk, Ben, Van Der Ploeg, Ans T, Pajkrt, Dasja, Nitz, Elisa, Van Den Hout, Johanna M.P, Van Der Post, Julie, Wolf, Nicole I, Beerepoot, Shanice, Groen, Ewout J.N, Tüngler, Victoria, Teunissen, Charlotte E

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Therapeutic Approaches to Type I Interferonopathies von Bienias, Marc, Brück, Normi, Griep, Constanze, Wolf, Christine, Kretschmer, Stefanie, Kind, Barbara, Tüngler, Victoria, Berner, Reinhard, Lee-Kirsch, Min Ae

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High association of MOG-IgG antibodies in children with bilateral optic neuritis von Wendel, Eva-Maria, Baumann, Matthias, Barisic, Nina, Blaschek, Astrid, Coelho de Oliveira Koch, Eliana, Della Marina, Adela, Diepold, Katharina, Hackenberg, Annette, Hahn, Andreas, von Kalle, Thekla, Karenfort, Michael, Kornek, Barbara, Lechner, Christian, Leiz, Steffen, Merkenschlager, Andreas, Nosadini, Margherita, Sartori, Stefano, Schanda, Kathrin, Schimmel, Mareike, Seemann, Larissa, Tüngler, Victoria, Waltz, Stephan, Wegener-Panzer, Andreas, Wiegand, Gert, Reindl, Markus, Rostásy, Kevin

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Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene von Schmelzer, Lisa, Smitka, Martin, Wolf, Christine, Lucas, Nadja, Tüngler, Victoria, Hahn, Gabriele, Tzschach, Andreas, Di Donato, Nataliya, Lee-Kirsch, Min Ae, von der Hagen, Maja

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Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome von Wendel, Eva Maria, Thonke, Helen Sophie, Bertolini, Annikki, Baumann, Matthias, Blaschek, Astrid, Merkenschlager, Andreas, Karenfort, Michael, Kornek, Barbara, Lechner, Christian, Pohl, Daniela, Pritsch, Martin, Schanda, Kathrin, Schimmel, Mareike, Thiels, Charlotte, Waltz, Stephan, Wiegand, Gert, Anlar, Banu, Barisic, Nina, Blank, Christian, Breu, Markus, Broser, Philip, Della Marina, Adela, Diepold, Katharina, Eckenweiler, Matthias, Eisenkölbl, Astrid, Freilinger, Michael, Gruber-Sedlmayr, Ursula, Hackenberg, Annette, Iff, Tobias, Knierim, Ellen, Koch, Johannes, Kutschke, Georg, Leiz, Steffen, Lischetzki, Grischa, Nosadini, Margherita, Pschibul, Alexander, Reiter-Fink, Edith, Rohrbach, Doris, Salandin, Michela, Sartori, Stefano, Schlump, Jan-Ulrich, Stoffels, Johannes, Strautmanis, Jurgis, Tibussek, Daniel, Tüngler, Victoria, Utzig, Norbert, Reindl, Markus, Rostásy, Kevin

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High association of MOG-IgG antibodies in children with bilateral optic neuritis von Wendel, Eva-Maria, Baumann, Matthias, Barisic, Nina, Blaschek, Astrid, Coelho de Oliveira Koch, Eliana, Della Marina, Adela, Diepold, Katharina, Hackenberg, Annette, Hahn, Andreas, von Kalle, Thekla, Karenfort, Michael, Kornek, Barbara, Lechner, Christian, Leiz, Steffen, Merkenschlager, Andreas, Nosadini, Margherita, Sartori, Stefano, Schanda, Kathrin, Schimmel, Mareike, Seemann, Larissa, Tüngler, Victoria, Waltz, Stephan, Wegener-Panzer, Andreas, Wiegand, Gert, Reindl, Markus, Rostásy, Kevin

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Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation von Tüngler, Victoria, Doebler-Neumann, Marion, Salandin, Michaela, Kaufmann, Peter, Wolf, Christine, Lucas, Nadja, Harmuth, Florian, Reichbauer, Jennifer, Krägeloh-Mann, Ingeborg, Schüle, Rebecca, Lee-Kirsch, Min Ae

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Naturally Occurring Genetic Variants of Human Caspase-1 Differ Considerably in Structure and the Ability to Activate Interleukin-1β von Luksch, Hella, Romanowski, Michael J., Chara, Osvaldo, Tüngler, Victoria, Caffarena, Ernesto R., Heymann, Michael C., Lohse, Peter, Aksentijevich, Ivona, Remmers, Elaine F., Flecks, Silvana, Quoos, Nadine, Gramatté, Johannes, Petzold, Cathleen, Hofmann, Sigrun R., Winkler, Stefan, Pessler, Frank, Kallinich, Tilmann, Ganser, Gerd, Nimtz-Talaska, Antje, Baumann, Ulrich, Runde, Volker, Grimbacher, Bodo, Birmelin, Jennifer, Gahr, Manfred, Roesler, Joachim, Rösen-Wolff, Angela

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Thymulin-Based Gene Therapy and Pituitary Function in Animal Models of Aging von Reggiani, Paula C., Poch, Brenda, Cónsole, Gloria M., Rimoldi, Omar J., Schwerdt, Jose I., Tüngler, Victoria, Garcia-Bravo, Margarita M., Dardenne, Mireille, Goya, Rodolfo G.

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Progesterone's activity in the central nervous system von Tüngler, Victoria

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Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T RNASEH2B Mutation von Tüngler, Victoria, Schmidt, Franziska, Hieronimus, Steve, Reyes-Velasco, Claudio, Lee-Kirsch, Min Ae

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