Personality factors in patients with myasthenia gravis: A prospective study von Jordan, Berit, Förster, Luise, Buchholz, Theresa, Sperfeld, Anne‐Dorte, Zierz, Stephan

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Whole brain-based analysis of regional white matter tract alterations in rare motor neuron diseases by diffusion tensor imaging von Unrath, Alexander, Müller, Hans-Peter, Riecker, Axel, Ludolph, Albert C., Sperfeld, Anne-Dorte, Kassubek, Jan

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Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue von Treiber, Nicolai, Maity, Pallab, Singh, Karmveer, Kohn, Matthias, Keist, Alexander F., Ferchiu, Florentina, Sante, Lea, Frese, Sebastian, Bloch, Wilhelm, Kreppel, Florian, Kochanek, Stefan, Sindrilaru, Anca, Iben, Sebastian, Högel, Josef, Ohnmacht, Michael, Claes, Lutz E., Ignatius, Anita, Chung, Jin H., Lee, Min J., Kamenisch, York, Berneburg, Mark, Nikolaus, Thorsten, Braunstein, Kerstin, Sperfeld, Anne‐Dorte, Ludolph, Albert C., Briviba, Karlis, Wlaschek, Meinhard, Scharffetter‐Kochanek, Karin

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Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD von Münch, Christoph, Rosenbohm, Angela, Sperfeld, Anne-Dorte, Uttner, Ingo, Reske, Sven, Krause, Bernd J., Sedlmeier, Reinhard, Meyer, Thomas, Hanemann, Clemens O., Stumm, Gabriele, Ludolph, Albert C.

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Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approach von Yilmaz, Ali, Gdynia, Hans-Jürgen, Baccouche, Hannibal, Mahrholdt, Heiko, Meinhardt, Gabriel, Basso, Cristina, Thiene, Gaetano, Sperfeld, Anne-Dorte, Ludolph, Albert C, Sechtem, Udo

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Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosis von Riecker, Axel, Kühnlein, Peter, Gdynia, Hans-Jürgen, Sperfeld, Anne-Dorte, Lindner-Pfleghar, Beate, Ludolph, Albert Christian, Prosiegel, Mario

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Frontotemporal cognitive function in X-linked spinal and bulbar muscular atrophy (SBMA): a controlled neuropsychological study of 20 patients von Soukup, Georg Rüdiger, Sperfeld, Anne-Dorte, Uttner, Ingo, Karitzky, Jochen, Ludolph, Albert Christian, Kassubek, Jan, Schreiber, Herbert

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The cerebro-morphological fingerprint of a progeroid syndrome: white matter changes correlate with neurological symptoms in xeroderma pigmentosum von Kassubek, Jan, Sperfeld, Anne-Dorte, Pinkhardt, Elmar H, Unrath, Alexander, Müller, Hans-Peter, Scharffetter-Kochanek, Karin, Ludolph, Albert C, Berneburg, Mark

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Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis von Kress, Julia A., Kühnlein, Peter, Winter, Pia, Ludolph, Albert C., Kassubek, Jan, Müller, Ulrich, Sperfeld, Anne-Dorte

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Restless Legs Syndrome in Hereditary Spastic Paraparesis von Sperfeld, Anne-Dorte, Unrath, Alexander, Kassubek, Jan

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Corticospinal tract MRI hyperintensity in X-linked Charcot-Marie-Tooth Disease von Kassubek, Jan, Bretschneider, Volker, Sperfeld, Anne-Dorte

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Diabetes Mellitus Is a Possible Risk Factor for Nodo-paranodopathy With Antiparanodal Autoantibodies von Appeltshauser, Luise, Messinger, Julia, Starz, Katharina, Heinrich, David, Brunder, Anna-Michelle, Stengel, Helena, Fiebig, Bianca, Ayzenberg, Ilya, Birklein, Frank, Dresel, Christian, Dorst, Johannes, Dvorak, Florian, Grimm, Alexander, Joerk, Alexander, Leypoldt, Frank, Mäurer, Mathias, Merl, Patrick, Michels, Sebastian, Pitarokoili, Kalliopi, Rosenfeldt, Mathias, Sperfeld, Anne-Dorte, Weihrauch, Marc, Welte, Gabriel Simon, Sommer, Claudia, Doppler, Kathrin

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Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic? von Felbecker, Ansgar, Camu, William, Valdmanis, Paul N, Sperfeld, Anne-Dorte, Waibel, Stefan, Steinbach, Peter, Rouleau, Guy A, Ludolph, Albert C, Andersen, Peter M

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User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study von Spittel, Susanne, Meyer, Thomas, Weyen, Ute, Grehl, Torsten, Weydt, Patrick, Steinbach, Robert, Petri, Susanne, Baum, Petra, Metelmann, Moritz, Sperfeld, Anne-Dorte, Kettemann, Dagmar, Norden, Jenny, Rödiger, Annekathrin, Ilse, Benjamin, Grosskreutz, Julian, Hildebrandt, Barbara, Walter, Bertram, Münch, Christoph, Maier, André

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Intravenous versus subcutaneous immunoglobulin – Authors' reply von Mielke, Orell, Roberts, Leslie, Carne, Ross, Blum, Stefan, Henderson, Robert, Van Damme, Philip, Demeestere, Jelle, Pinard D'Amour, Catherine-Andree, Bril, Vera, Breiner, Ari, Sussova, Jana, Kalous, Tomas, Talab, Radomir, Toomsoo, Toomas, Rubanovits, Inna, Gross-Paju, Katrin, Saarela, Mika, Pouget, Jean, Wielanek-Bachelet, Anne-Cécile, Desnuelle, Claude, Clavelou, Pierre, Zschuentssch, Jana, Kramer, Daniela, Hoffmann, Olaf, Goerlitz, Carsten, Yoon, Min-Suk, Gold, Ralf, Berlit, Peter, Jaspert-Grehl, Andrea, Kutschenko, Anna, Trebst, Corinna, Baum, Petra, Then Bergh, Florian, Klehmet, Juliane, Klostermann, Fabian, Oechtering, Johanna, Lehmann, Helmar, Mueller, Daniel, Yarnitsky, David, Di Muzio, Antonio, Ciccocioppo, Fausta, Sorbi, Sandro, Mata, Sabrina, Schenone, Angelo, Grandis, Marina, Lauria, Giuseppe, Cazzato, Daniele, Antonini, Giovanni, Zibetti, Maurizio, Yokota, Takanori, Kuwabara, Satoshi, Mori, Masahiro, Iijima, Masahiro, Tomiyama, Masahiko, Akutsu, Tsugio, Yokoyama, Kazumasa, Kanai, Kazuaki, Eftimov, Filip, Notermans, Nicolette. C., Visser, Nora. A., Hoeijmakers, Janneke. G.J., Merkies, Ingemar S.J., van Geloven, Nan, Rejdak, Konrad, Casanovas Pons, Carlos, Alberti Aguiló, María Antonia, Gamez, Josep, Figueras, María, Marquez Infante, Celedonio, Benitez Rivero, Sonia, Lunn, Michael, Morrow, Jasper, Gosal, David, Lavin, Timothy Myles, Melamed, Isaac, Ajroud-Driss, Senda, Simpson, Ericka, Chi-Ho Lai, Eugene, Dimachkie, Mazen, Barohn, Richard J., Beydoun, Said, Johl, Harpreet, Shtilbans, Alexander, Muley, Suraj, Freimer, Miriam, Kissel, John, Latov, Norman, Ubogu, Eroboghene, Mumfrey, Sandi, Rao, T. Hermanth P., MacDonald, Paul, Sharma, Khema, Gonzalez, Ginna, Walk, David, Gable, Karissa, Lewis, Richard A., Cornblath, David R., Lawo, John-Phillip, Praus, Michaela, Durn, Billie L.

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Magnetic Resonance Investigation of the Upper Spinal Cord in Pure and Complicated Hereditary Spastic Paraparesis von Sperfeld, Anne-Dorte, Baumgartner, Annette, Kassubek, Jan

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Cardiac involvement in a female carrier of Duchenne muscular dystrophy von Walcher, Thomas, Kunze, Markus, Steinbach, Peter, Sperfeld, Anne-Dorte, Burgstahler, Christof, Hombach, Vinzenz, Torzewski, Jan

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The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases von Arning, Larissa, Epplen, Jörg T., Rahikkala, Elisa, Hendrich, Corinna, Ludolph, Albert C., Sperfeld, Anne-Dorte

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Laryngospasm: An underdiagnosed symptom of X-linked spinobulbar muscular atrophy von SPERFELD, Anne-Dorte, HANEMANN, C. Oliver, LUDOLPH, Albert C, KASSUBEK, Jan

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Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis von Fernández-Santiago, Rubén, Hoenig, Sabine, Lichtner, Peter, Sperfeld, Anne-Dorte, Sharma, Manu, Berg, Daniela, Weichenrieder, Oliver, Illig, Thomas, Eger, Katharina, Meyer, Thomas, Anneser, Johanna, Münch, Christoph, Zierz, Stephan, Gasser, Thomas, Ludolph, Albert

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