Bücherbesprechungen by Zieger, Teichmann, Gerlach, Walther, Dänzer, Hermann, Krebs, Adolf, Knöll, Ostwald, Wo, Rudder, Thierbach, Steger, W., Haas, J. R., Miekeley

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Hot-spot KIF5A mutations cause familial ALS by 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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CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency by Brockmann, Sarah J, Freischmidt, Axel, Oeckl, Patrick, Müller, Kathrin, Ponna, Srinivas K, Helferich, Anika M, Paone, Christoph, Reinders, Jörg, Kojer, Kerstin, Orth, Michael, Jokela, Manu, Auranen, Mari, Udd, Bjarne, Hermann, Andreas, Danzer, Karin M, Lichtner, Peter, Walther, Paul, Ludolph, Albert C, Andersen, Peter M, Otto, Markus, Kursula, Petri, Just, Steffen, Weishaupt, Jochen H

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SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden by Yilmaz, Rüstem, Müller, Kathrin, Brenner, David, Volk, Alexander E., Borck, Guntram, Hermann, Andreas, Meitinger, Thomas, Strom, Tim M., Danzer, Karin M., Ludolph, Albert C., Andersen, Peter M., Weishaupt, Jochen H., Weyen, Ute, Hermann, Andreas, Regensburger, Martin, Winkler, Jürgen, Linker, Ralf, Winner, Beate, Hagenacker, Tim, Koch, Jan Christoph, Lingor, Paul, Göricke, Bettina, Zierz, Stephan, Jordan, Berit, Baum, Petra, Wolf, Joachim, Winkler, Andrea, Young, Peter, Bogdahn, Ulrich, Prudlo, Johannes, Kassubek, Jan

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A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis by Freischmidt, Axel, Goswami, Anand, Limm, Katharina, Zimyanin, Vitaly L, Demestre, Maria, Glaß, Hannes, Holzmann, Karlheinz, Helferich, Anika M, Brockmann, Sarah J, Tripathi, Priyanka, Yamoah, Alfred, Poser, Ina, Oefner, Peter J, Böckers, Tobias M, Aronica, Eleonora, Ludolph, Albert C, Andersen, Peter M, Hermann, Andreas, Weis, Joachim, Reinders, Jörg, Danzer, Karin M, Weishaupt, Jochen H

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Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations by 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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