Effect of High‐Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis von Ludolph, Albert C., Dorst, Johannes, Dreyhaupt, Jens, Weishaupt, Jochen H., Kassubek, Jan, Weiland, Ulrike, Meyer, Thomas, Petri, Susanne, Hermann, Andreas, Emmer, Alexander, Grosskreutz, Julian, Grehl, Torsten, Zeller, Daniel, Boentert, Matthias, Schrank, Bertold, Prudlo, Johannes, Winkler, Andrea S., Gorbulev, Stanislav, Roselli, Francesco, Schuster, Joachim, Dupuis, Luc

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Mutation in TACO1 , encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome von Chevrette, Mario, Antonicka, Hana, Weraarpachai, Woranontee, Sasarman, Florin, Shoubridge, Eric A, Schrank, Bertold, Kaufman, Brett A, Kolesar, Jill E, Lochmüller, Hanns, Horvath, Rita, Seeger, Jürgen

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Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study von Dorst, Johannes, Dupuis, Luc, Petri, Susanne, Kollewe, Katja, Abdulla, Susanne, Wolf, Joachim, Weber, Markus, Czell, David, Burkhardt, Christian, Hanisch, Frank, Vielhaber, Stefan, Meyer, Thomas, Frisch, Gabriele, Kettemann, Dagmar, Grehl, Torsten, Schrank, Bertold, Ludolph, Albert C.

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A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosis von Dupuis, Luc, Dengler, Reinhard, Heneka, Michael T, Meyer, Thomas, Zierz, Stephan, Kassubek, Jan, Fischer, Wilhelm, Steiner, Franziska, Lindauer, Eva, Otto, Markus, Dreyhaupt, Jens, Grehl, Torsten, Hermann, Andreas, Winkler, Andrea S, Bogdahn, Ulrich, Benecke, Reiner, Schrank, Bertold, Wessig, Carsten, Grosskreutz, Julian, Ludolph, Albert C

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Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy von Winter, Yaroslav, Schepelmann, Karsten, Spottke, Annika E., Claus, Detlef, Grothe, Christoph, Schröder, Rolf, Heuss, Dieter, Vielhaber, Stefan, Tackenberg, Björn, Mylius, Veit, Reese, Jens-Peter, Kiefer, Reinhard, Schrank, Bertold, Oertel, Wolfgang H., Dodel, Richard

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Socioeconomic burden of amyotrophic lateral sclerosis, myasthenia gravis and facioscapulohumeral muscular dystrophy von Schepelmann, Karsten, Winter, Yaroslav, Spottke, Annika E., Claus, Detlef, Grothe, Christoph, Schröder, Rolf, Heuss, Dieter, Vielhaber, Stefan, Mylius, Veit, Kiefer, Reinhard, Schrank, Bertold, Oertel, Wolfgang H., Dodel, Richard

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Inactivation of the Survival Motor Neuron Gene, a Candidate Gene for Human Spinal Muscular Atrophy, Leads to Massive Cell Death in Early Mouse Embryos von Schrank, Bertold, Gotz, Rudolf, Gunnersen, Jennifer M., Ure, Janice M., Toyka, Klaus V., Smith, Austin G., Sendtner, Michael

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Interaction Between a Putative Mechanosensory Membrane Channel and a Collagen von Liu, Jingdong, Schrank, Bertold, Waterston, Robert H.

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End of life perspectives: a systematic survey of patients with amyotrophic lateral sclerosis von Eickhoff, Clemens, Schöne-Seifert, Bettina, Kettemann, Dagmar, Bormann, Eike, Grehl, Torsten, Boentert, Matthias, Koch, Jan C, Schmitt, Carolina, Schrank, Bertold, Schröter, Carsten, Meyer, Thomas

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Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease von Keller, Natalie, Paketci, Cem, Altmueller, Janine, Fuhrmann, Nico, Wunderlich, Gilbert, Schrank, Bertold, Unver, Olcay, Yilmaz, Sanem, Boostani, Reza, Karimiani, Ehsan Ghayoor, Motameny, Susanne, Thiele, Holger, Nürnberg, Peter, Maroofian, Reza, Yis, Uluc, Wirth, Brunhilde, Karakaya, Mert

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Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies von Dohrn, Maike F., Glöckle, Nicola, Mulahasanovic, Lejla, Heller, Corina, Mohr, Julia, Bauer, Christine, Riesch, Erik, Becker, Andrea, Battke, Florian, Hörtnagel, Konstanze, Hornemann, Thorsten, Suriyanarayanan, Saranya, Blankenburg, Markus, Schulz, Jörg B., Claeys, Kristl G., Gess, Burkhard, Katona, Istvan, Ferbert, Andreas, Vittore, Debora, Grimm, Alexander, Wolking, Stefan, Schöls, Ludger, Lerche, Holger, Korenke, G. Christoph, Fischer, Dirk, Schrank, Bertold, Kotzaeridou, Urania, Kurlemann, Gerhard, Dräger, Bianca, Schirmacher, Anja, Young, Peter, Schlotter‐Weigel, Beate, Biskup, Saskia

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Targeted sequencing with expanded gene profile enables high diagnostic yield in non‐5q‐spinal muscular atrophies von Karakaya, Mert, Storbeck, Markus, Strathmann, Eike A., Delle Vedove, Andrea, Hölker, Irmgard, Altmueller, Janine, Naghiyeva, Leyla, Schmitz‐Steinkrüger, Lea, Vezyroglou, Katharina, Motameny, Susanne, Alawbathani, Salem, Thiele, Holger, Polat, Ayse Ipek, Okur, Derya, Boostani, Reza, Karimiani, Ehsan Ghayoor, Wunderlich, Gilbert, Ardicli, Didem, Topaloglu, Haluk, Kirschner, Janbernd, Schrank, Bertold, Maroofian, Reza, Magnusson, Olafur, Yis, Uluc, Nürnberg, Peter, Heller, Raoul, Wirth, Brunhilde

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Prognostic factors in ALS: a comparison between Germany and China von Dorst, Johannes, Chen, Lu, Rosenbohm, Angela, Dreyhaupt, Jens, Hübers, Annemarie, Schuster, Joachim, Weishaupt, Jochen H., Kassubek, Jan, Gess, Burkhard, Meyer, Thomas, Weyen, Ute, Hermann, Andreas, Winkler, Jürgen, Grehl, Torsten, Hagenacker, Tim, Lingor, Paul, Koch, Jan C., Sperfeld, Anne, Petri, Susanne, Großkreutz, Julian, Metelmann, Moritz, Wolf, Joachim, Winkler, Andrea S., Klopstock, Thomas, Boentert, Matthias, Johannesen, Siw, Storch, Alexander, Schrank, Bertold, Zeller, Daniel, Liu, Xiao-lu, Tang, Lu, Fan, Dong-Sheng, Ludolph, Albert C.

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De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation von Mendoza-Ferreira, Natalia, Karakaya, Mert, Cengiz, Nur, Beijer, Danique, Brigatti, Karlla W., Gonzaga-Jauregui, Claudia, Fuhrmann, Nico, Hölker, Irmgard, Thelen, Maximilian P., Zetzsche, Sebastian, Rombo, Roman, Puffenberger, Erik G., De Jonghe, Peter, Deconinck, Tine, Zuchner, Stephan, Strauss, Kevin A., Carson, Vincent, Schrank, Bertold, Wunderlich, Gilbert, Baets, Jonathan, Wirth, Brunhilde

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Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency von Schrank, Bertold, Schoser, Benedikt, Klopstock, Thomas, Schneiderat, Peter, Horvath, Rita, Abicht, Angela, Holinski-Feder, Elke, Augustis, Sarunas

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Effect of High-Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis (Nov, 10.1002/ana.25661, 2019 von Ludolph, Albert C., Dorst, Johannes, Dreyhaupt, Jens, Weishaupt, Jochen H., Kassubek, Jan, Weiland, Ulrike, Meyer, Thomas, Petri, Susanne, Hermann, Andreas, Jordan, Berit, Grosskreutz, Julian, Grehl, Torsten, Zeller, Daniel, Boentert, Matthias, Schrank, Bertold, Prudlo, Johannes, Winkler, Andrea S., Gorbulev, Stanislav, Roselli, Francesco, Schuster, Joachim, Dupuis, Luc

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Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial von Walter, Maggie C, Reilich, Peter, Thiele, Simone, Schessl, Joachim, Schreiber, Herbert, Reiners, Karlheinz, Kress, Wolfram, Müller-Reible, Clemens, Vorgerd, Matthias, Urban, Peter, Schrank, Bertold, Deschauer, Marcus, Schlotter-Weigel, Beate, Kohnen, Ralf, Lochmüller, Hanns

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Novel variants broaden the phenotypic spectrum of PLEKHG5‐associated neuropathies von Chen, Zhongbo, Maroofian, Reza, Başak, A. Nazlı, Shingavi, Leena, Karakaya, Mert, Efthymiou, Stephanie, Gustavsson, Emil K., Meier, Leyla, Polavarapu, Kiran, Vengalil, Seena, Preethish‐Kumar, Veeramani, Nandeesh, Bevinahalli N., Gökçe Güneş, Nalan, Akan, Onur, Candan, Fatma, Schrank, Bertold, Zuchner, Stephan, Murphy, David, Kapoor, Mahima, Ryten, Mina, Wirth, Brunhilde, Reilly, Mary M., Nalini, Atchayaram, Houlden, Henry, Sarraf, Payam

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Muscle MRI findings in limb girdle muscular dystrophy type 2L von Sarkozy, Anna, Deschauer, Marcus, Carlier, Robert-Yves, Schrank, Bertold, Seeger, Jürgen, Walter, Maggie C, Schoser, Benedikt, Reilich, Peter, Leturq, France, Radunovic, Aleksandar, Behin, Anthony, Laforet, Pascal, Eymard, Bruno, Schreiber, Herbert, Hicks, Debbie, Vaidya, Sujit S, Gläser, Dieter, Carlier, Pierre G, Bushby, Kate, Lochmüller, Hanns, Straub, Volker

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Different Patterns of Autoantibody Secretion by Peripheral Blood Mononuclear Cells in Autoimmune Nodopathies von Rohrbacher, Sophia, Seefried, Sabine, Hartmannsberger, Beate, Annabelle, Rosa, Appeltshauser, Luise, Arlt, Friederike A, Brämer, Dirk, Dresel, Christian, Dorst, Johannes, Elmas, Zeynep, Franke, Christiana, Geis, Christian, Högen, Tobias, Krause, Sabine, Marziniak, Martin, Mäurer, Mathias, Prüss, Harald, Schoeberl, Florian, Schrank, Bertold, Steen, Claudia, Teichtinger, Helena, Thieme, Andrea, Wessely, Lena, Zernecke, Alma, Sommer, Claudia, Doppler, Kathrin

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