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2021
Lohmann, Lisa 
ORCID: 0000-0003-4911-6883, Lammerskitten, Anna, Korsen, Melanie, Dodel, Richard, Gaul, Charly, Hamer, Hajo M., Kleineberg, Nina N., Ludolph, Albert C., Mayer, Geert, Poli, Sven ORCID: 0000-0002-0286-8781, Saur, Dorothee ORCID: 0000-0002-1808-0913, Steinhoff, Bernhard J., Timmermann, Lars, Klotz, Luisa and Meuth, Sven G.
(2021).
Status of clinical research in neurology in Germany-A national survey.
Eur. J. Neurol., 28 (5).
S. 1446 - 1453.
HOBOKEN:
WILEY.
ISSN 1468-1331
2020
Hagenacker, Tim, Wurster, Claudia D., Guenther, Rene, Schreiber-Katz, Olivia, Osmanovic, Alma, Petri, Susanne, Weiler, Markus, Ziegler, Andreas, Kuttler, Josua, Koch, Jan C., Schneider, Ilka, Wunderlich, Gilbert, Schloss, Natalie, Lehmann, Helmar C., Cordts, Isabell, Deschauer, Marcus, Lingor, Paul ORCID: 0000-0001-9362-7096, Kamm, Christoph, Stolte, Benjamin, Pietruck, Lena, Totzeck, Andreas, Kizina, Kathrin, Monninghoff, Christoph, von Velsen, Otgonzul, Ose, Claudia, Reichmann, Heinz, Forsting, Michael, Pechmann, Astrid, Kirschner, Janbernd, Ludolph, Albert C., Hermann, Andreas and Kleinschnitz, Christoph
(2020).
Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study.
Lancet Neurol., 19 (4).
S. 317 - 326.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1474-4465
2019
Spruegel, Maximilian I., Sembill, Jochen A. ORCID: 0000-0003-0014-3389, Kuramatsu, Joji B., Gerner, Stefan T., Hagen, Manuel, Roeder, Sebastian S., Endres, Matthias, Haeusler, Karl Georg, Sobesky, Jan, Schurig, Johannes, Zweynert, Sarah, Bauer, Miriam, Vajkoczy, Peter, Ringleb, Peter Arthur, Purrucker, Jan Christoph, Rizos, Timolaos, Volkmann, Jens, Muellges, Wolfgang, Kraft, Peter, Schubert, Anna-Lena, Erbguth, Frank, Nueckel, Martin, Schellinger, Peter D., Glahn, Joerg, Knappe, Ulrich J., Fink, Gereon Rudolf, Dohmen, Christian, Stetefeld, Henning, Fisse, Anna Lena, Minnerup, Jens, Hagemann, Georg, Rakers, Florian, Reichmann, Heinz, Schneider, Hauke ORCID: 0000-0002-9641-0922, Woepking, Sigrid, Ludolph, Albert C., Stosser, Sebastian, Neugebauer, Hermann ORCID: 0000-0003-3759-356X, Roether, Joachim, Michels, Peter, Schwarz, Michael, Reimann, Gernot, Baezner, Hansjoerg, Schwert, Henning, Classen, Joseph ORCID: 0000-0001-7182-6967, Michalski, Dominik, Grau, Armin, Palm, Frederick, Urbanek, Christian, Woehrle, Johannes C., Alshammari, Fahid, Horn, Markus, Bahner, Dirk, Witte, Otto W., Guenther, Albrecht, Hamann, Gerhard F., Luecking, Hannes, Doerfler, Arnd, Schwab, Stefan and Huttner, Hagen B.
(2019).
Heparin for prophylaxis of venous thromboembolism in intracerebral haemorrhage.
J. Neurol. Neurosurg. Psychiatry, 90 (7).
S. 783 - 792.
LONDON:
BMJ PUBLISHING GROUP.
ISSN 1468-330X
2017
Tuerk, Matthias, Schroeder, Rolf, Khuller, Katharina, Hofmann, Andreas ORCID: 0000-0003-4408-5467, Berwanger, Carolin, Ludolph, Albert C., Dekomien, Gabriele, Mueller, Kathrin, Weishaupt, Jochen H., Thiel, Christian T. and Clemen, Christoph S.
(2017).
Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients.
Neurobiol. Aging, 56.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1558-1497
van Doormaal, Perry T. C., Ticozzi, Nicola ORCID: 0000-0001-5963-7426, Weishaupt, Jochen H., Kenna, Kevin, Diekstra, Frank P., Verde, Federico ORCID: 0000-0002-3977-6995, Andersen, Peter M., Dekker, Annelot M., Tiloca, Cinzia, Marroquin, Nicolai, Overste, Daniel J., Pensato, Viviana ORCID: 0000-0001-9798-2669, Nuernberg, Peter, Pulit, Sara L., Schellevis, Raymond D., Calini, Daniela, Altmueller, Janine, Francioli, Laurent C., Muller, Bernard, Castellotti, Barbara, Motameny, Susanne, Ratti, Antonia, Wolf, Joachim, Gellera, Cinzia, Ludolph, Albert C., van den Berg, Leonard H., Kubisch, Christian ORCID: 0000-0003-4220-0978, Landers, John E., Veldink, Jan H., Silani, Vincenzo and Volk, Alexander E.
(2017).
The role of de novo mutations in the development of amyotrophic lateral sclerosis.
Hum. Mutat., 38 (11).
S. 1534 - 1542.
HOBOKEN:
WILEY.
ISSN 1098-1004
2015
Huebers, Annemarie, Just, Walter, Rosenbohm, Angela, Mueller, Kathrin, Marroquin, Nicolai, Goebel, Ingrid, Hoegel, Josef, Thiele, Holger, Altmueller, Janine, Nuernberg, Peter, Weishaupt, Jochen H., Kubisch, Christian ORCID: 0000-0003-4220-0978, Ludolph, Albert C. and Volk, Alexander E.
(2015).
De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
Neurobiol. Aging, 36 (11).
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1558-1497