Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis von Weydt, Patrick, Oeckl, Patrick, Huss, André, Müller, Kathrin, Volk, Alexander E., Kuhle, Jens, Knehr, Antje, Andersen, Peter M., Prudlo, Johannes, Steinacker, Petra, Weishaupt, Jochen H., Ludolph, Albert C., Otto, Markus

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Impaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients von Yazar, Volkan, Kühlwein, Julia K., Knehr, Antje, Grozdanov, Veselin, Ekici, Arif B., Ludolph, Albert C., Danzer, Karin M.

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Eye movement alterations in presymptomatic C9orf72 expansion gene carriers von Behler, Anna, Knehr, Antje, Finsel, Julia, Kunz, Martin S., Lang, Christina, Müller, Kathrin, Müller, Hans-Peter, Pinkhardt, Elmar H., Ludolph, Albert C., Lulé, Dorothée, Kassubek, Jan

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FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees von Brenner, David, Müller, Kathrin, Lattante, Serena, Yilmaz, Rüstem, Knehr, Antje, Freischmidt, Axel, Ludolph, Albert C., Andersen, Peter M., Weishaupt, Jochen H.

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Quadruple genetic variants in a sporadic ALS patient von Yilmaz, Rüstem, Weishaupt, Kanchi, Valkadinov, Ivan, Knehr, Antje, Brenner, David, Weishaupt, Jochen H.

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Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder von Lulé, Dorothée E., Müller, Hans-Peter, Finsel, Julia, Weydt, Patrick, Knehr, Antje, Winroth, Ivar, Andersen, Peter M., Weishaupt, Jochen, Uttner, Ingo, Kassubek, Jan, Ludolph, Albert C.

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Hot-spot KIF5A mutations cause familial ALS von Brenner, David, Yilmaz, Rüstem, Müller, Kathrin, Grehl, Torsten, Petri, Susanne, Meyer, Thomas, Grosskreutz, Julian, Weydt, Patrick, Ruf, Wolfgang, Neuwirth, Christoph, Weber, Markus, Pinto, Susana, Claeys, Kristl G, Schrank, Berthold, Jordan, Berit, Knehr, Antje, Günther, Kornelia, Hübers, Annemarie, Zeller, Daniel, Kubisch, Christian, Jablonka, Sibylle, Sendtner, Michael, Klopstock, Thomas, de Carvalho, Mamede, Sperfeld, Anne, Borck, Guntram, Volk, Alexander E, Dorst, Johannes, Weis, Joachim, Otto, Markus, Schuster, Joachim, Del Tredici, Kelly, Braak, Heiko, Danzer, Karin M, Freischmidt, Axel, Meitinger, Thomas, Strom, Tim M, Ludolph, Albert C, Andersen, Peter M, Weishaupt, Jochen H

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Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells von Ruf, Wolfgang P., Hannon, Eilis, Freischmidt, Axel, Grozdanov, Veselin, Brenner, David, Müller, Kathrin, Knehr, Antje, Günther, Kornelia, Dorst, Johannes, Ammerpohl, Ole, Danzer, Karin M., Mill, Jonathan, Ludolph, Albert C., Weishaupt, Jochen H.

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Clinical characterization of common pathogenic variants of SOD1-ALS in Germany von Wiesenfarth, Maximilian, Forouhideh-Wiesenfarth, Yalda, Elmas, Zeynep, Parlak, Özlem, Weiland, Ulrike, Herrmann, Christine, Schuster, Joachim, Freischmidt, Axel, Müller, Kathrin, Siebert, Reiner, Günther, Kornelia, Fröhlich, Elke, Knehr, Antje, Simak, Tatiana, Bachhuber, Franziska, Regensburger, Martin, Petri, Susanne, Klopstock, Thomas, Reilich, Peter, Schöberl, Florian, Schumann, Peggy, Körtvélyessy, Peter, Meyer, Thomas, Ruf, Wolfgang P., Witzel, Simon, Tumani, Hayrettin, Brenner, David, Dorst, Johannes, Ludolph, Albert C.

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A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification von Forouhideh, Yalda, Müller, Kathrin, Ruf, Wolfgang, Assi, Muhannad, Şeker, Tuncay, Tunca, Ceren, Knehr, Antje, Strom, Tim M, Gorges, Martin, Schradt, Falk, Meitinger, Thomas, Ludolph, Albert C, Pinkhardt, Elmar H, Başak, A Nazlı, Kassubek, Jan, Uttner, Ingo, Weishaupt, Jochen H

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Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriers von Dorst, Johannes, Weydt, Patrick, Brenner, David, Witzel, Simon, Kandler, Katharina, Huss, André, Herrmann, Christine, Wiesenfarth, Maximilian, Knehr, Antje, Günther, Kornelia, Müller, Kathrin, Weishaupt, Jochen H., Prudlo, Johannes, Forsberg, Karin, Andersen, Peter M., Rosenbohm, Angela, Schuster, Joachim, Roselli, Francesco, Dupuis, Luc, Mayer, Benjamin, Tumani, Hayrettin, Kassubek, Jan, Ludolph, Albert C.

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Effects of tofersen treatment in patients with SOD1-ALS in a “real-world” setting – a 12-month multicenter cohort study from the German early access program von Wiesenfarth, Maximilian, Dorst, Johannes, Brenner, David, Elmas, Zeynep, Parlak, Özlem, Uzelac, Zeljko, Kandler, Katharina, Mayer, Kristina, Weiland, Ulrike, Herrmann, Christine, Schuster, Joachim, Freischmidt, Axel, Müller, Kathrin, Siebert, Reiner, Bachhuber, Franziska, Simak, Tatiana, Günther, Kornelia, Fröhlich, Elke, Knehr, Antje, Regensburger, Martin, German, Alexander, Petri, Susanne, Grosskreutz, Julian, Klopstock, Thomas, Reilich, Peter, Schöberl, Florian, Hagenacker, Tim, Weyen, Ute, Günther, René, Vidovic, Maximilian, Jentsch, Martin, Haarmeier, Thomas, Weydt, Patrick, Valkadinov, Ivan, Hesebeck-Brinckmann, Jasper, Conrad, Julian, Weishaupt, Jochen Hans, Schumann, Peggy, Körtvélyessy, Peter, Meyer, Thomas, Ruf, Wolfgang Philipp, Witzel, Simon, Senel, Makbule, Tumani, Hayrettin, Ludolph, Albert Christian

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DNA Methylation Analysis in Monozygotic Twins Discordant for ALS in Blood Cells von Yazar, Volkan, Ruf, Wolfgang P, Knehr, Antje, Günther, Kornelia, Ammerpohl, Ole, Danzer, Karin M, Ludolph, Albert C

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Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase von Oeckl, Patrick, Weydt, Patrick, Steinacker, Petra, Anderl-Straub, Sarah, Nordin, Frida, Volk, Alexander E, Diehl-Schmid, Janine, Andersen, Peter M, Kornhuber, Johannes, Danek, Adrian, Fassbender, Klaus, Fliessbach, Klaus, Jahn, Holger, Lauer, Martin, Mueller, Kathrin, Knehr, Antje, Prudlo, Johannes, Schneider, Anja, Thal, Dietmar R, Yilmazer-Hanke, Deniz, Weishaupt, Jochen H, Ludolph, Albert C, Otto, Markus

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Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis von Ruf, Wolfgang P, Boros, Matej, Freischmidt, Axel, Brenner, David, Grozdanov, Veselin, de Meirelles, Joao, Meyer, Thomas, Grehl, Torsten, Petri, Susanne, Grosskreutz, Julian, Weyen, Ute, Guenther, Rene, Regensburger, Martin, Hagenacker, Tim, Koch, Jan C, Emmer, Alexander, Roediger, Annekathrin, Steinbach, Robert, Wolf, Joachim, Weishaupt, Jochen H, Lingor, Paul, Deschauer, Marcus, Cordts, Isabell, Klopstock, Thomas, Reilich, Peter, Schoeberl, Florian, Schrank, Berthold, Zeller, Daniel, Hermann, Andreas, Knehr, Antje, Günther, Kornelia, Dorst, Johannes, Schuster, Joachim, Siebert, Reiner, Ludolph, Albert C, Müller, Kathrin

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Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriersResearch in context von Johannes Dorst, Patrick Weydt, David Brenner, Simon Witzel, Katharina Kandler, André Huss, Christine Herrmann, Maximilian Wiesenfarth, Antje Knehr, Kornelia Günther, Kathrin Müller, Jochen H. Weishaupt, Johannes Prudlo, Karin Forsberg, Peter M. Andersen, Angela Rosenbohm, Joachim Schuster, Francesco Roselli, Luc Dupuis, Benjamin Mayer, Hayrettin Tumani, Jan Kassubek, Albert C. Ludolph

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Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations von Brenner, David, Rosenbohm, Angela, Yilmaz, Rüstem, Müller, Kathrin, Grehl, Torsten, Petri, Susanne, Meyer, Thomas, Grosskreutz, Julian, Weydt, Patrick, Ruf, Wolfgang, Neuwirth, Christoph, Weber, Markus, Pinto, Susana, Claeys, Kristl G, Schrank, Berthold, Jordan, Berit, Knehr, Antje, Günther, Kornelia, Hübers, Annemarie, Zeller, Daniel, Kubisch, Christian, Jablonka, Sibylle, Sendtner, Michael, Klopstock, Thomas, de Carvalho, Mamede, Sperfeld, Anne, Borck, Guntram, Volk, Alexander E, Dorst, Johannes, Weis, Joachim, Otto, Markus, Schuster, Joachim, Del Tredici, Kelly, Braak, Heiko, Danzer, Karin M, Freischmidt, Axel, Meitinger, Thomas, Ludolph, Albert C, Andersen, Peter M, Weishaupt, Jochen H

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Effects of tofersen treatment in patients with SOD1-ALS in a “real-world” setting – a 12-month multicenter cohort study from the German early access programResearch in context... von Maximilian Wiesenfarth, Johannes Dorst, David Brenner, Zeynep Elmas, Özlem Parlak, Zeljko Uzelac, Katharina Kandler, Kristina Mayer, Ulrike Weiland, Christine Herrmann, Joachim Schuster, Axel Freischmidt, Kathrin Müller, Reiner Siebert, Franziska Bachhuber, Tatiana Simak, Kornelia Günther, Elke Fröhlich, Antje Knehr, Martin Regensburger, Alexander German, Susanne Petri, Julian Grosskreutz, Thomas Klopstock, Peter Reilich, Florian Schöberl, Tim Hagenacker, Ute Weyen, René Günther, Maximilian Vidovic, Martin Jentsch, Thomas Haarmeier, Patrick Weydt, Ivan Valkadinov, Jasper Hesebeck-Brinckmann, Julian Conrad, Jochen Hans Weishaupt, Peggy Schumann, Peter Körtvélyessy, Thomas Meyer, Wolfgang Philipp Ruf, Simon Witzel, Makbule Senel, Hayrettin Tumani, Albert Christian Ludolph

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Effects of tofersen treatment in patients with SOD1-ALS in a real-world setting - a 12-month multicenter cohort study from the German early access program von Wiesenfarth, Maximilian, Dorst, Johannes, Brenner, David, Elmas, Zeynep, Parlak, Oezlem, Uzelac, Zeljko, Kandler, Katharina, Mayer, Kristina, Weiland, Ulrike, Herrmann, Christine, Schuster, Joachim, Freischmidt, Axel, Mueller, Kathrin, Siebert, Reiner, Bachhuber, Franziska, Simak, Tatiana, Guenther, Kornelia, Froehlich, Elke, Knehr, Antje, Regensburger, Martin, German, Alexander, Petri, Susanne, Grosskreutz, Julian, Klopstock, Thomas, Reilich, Peter, Schoeberl, Florian, Hagenacker, Tim, Weyen, Ute, Guenther, Rene, Vidovic, Maximilian, Jentsch, Martin, Haarmeier, Thomas, Weydt, Patrick, Valkadinov, Ivan, Hesebeck-Brinckmann, Jasper, Conrad, Julian, Weishaupt, Jochen Hans, Schumann, Peggy, Koertvelyessy, Peter, Meyer, Thomas, Ruf, Wolfgang Philipp, Witzel, Simon, Senel, Makbule, Tumani, Hayrettin, Ludolph, Albert Christian

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A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification von Forouhideh, Yalda, Mueller, Kathrin, Ruf, Wolfgang, Assi, Muhannad, Seker, Tuncay, Tunca, Ceren, Knehr, Antje, Strom, Tim M, Gorges, Martin, Schradt, Falk, Meitinger, Thomas, Ludolph, Albert C, Pinkhardt, Elmar H, Basak, A. Nazli, Kassubek, Jan, Uttner, Ingo, Weishaupt, Jochen H

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