Search Results - Lindig, Tobias
- Showing 1 - 18 results of 18
-
1
-
2
-
3
-
4
-
5
-
6
-
7
Encephalopathic Susac’s Syndrome associated with livedo racemosa in a young woman before the completion of family planning by Engeholm, Maik, Leo-Kottler, Beate, Rempp, Hansjörg, Lindig, Tobias, Lerche, Holger, Kleffner, Ilka, Henes, Melanie, Dihné, Marcel
Published 2013Text -
8
-
9
GLINT: GlucoCEST in neoplastic tumors at 3 T—clinical results of GlucoCEST in gliomas by Bender, Benjamin, Herz, Kai, Deshmane, Anagha, Richter, Vivien, Tabatabai, Ghazaleh, Schittenhelm, Jens, Skardelly, Marco, Scheffler, Klaus, Ernemann, Ulrike, Kim, Mina, Golay, Xavier, Zaiss, Moritz, Lindig, Tobias
Published 2021Text -
10
X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation by Synofzik, Matthis, Müller vom Hagen, Jennifer, Haack, Tobias B, Wilhelm, Christian, Lindig, Tobias, Beck-Wödl, Stefanie, Nabuurs, Sander B, van Kuilenburg, André BP, de Brouwer, Arjan PM, Schöls, Ludger
Published 2014Text -
11
White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease by Sartor, Jennifer, Bettecken, Kristina, Bernhard, Felix P., Hofmann, Marc, Gladow, Till, Lindig, Tobias, Ciliz, Meltem, ten Kate, Mara, Geritz, Johanna, Heinzel, Sebastian, Benedictus, Marije, Scheltens, Philip, Hobert, Markus A., Maetzler, Walter
Published 2017Text -
12
Corrigendum: White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease by Sartor, Jennifer, Bettecken, Kristina, Bernhard, Felix P., Hofmann, Marc, Gladow, Till, Lindig, Tobias, Ciliz, Meltem, ten Kate, Mara, Geritz, Johanna, Heinzel, Sebastian, Benedictus, Marije, Scheltens, Philip, Hobert, Markus A., Maetzler, Walter
Published 2017Text -
13
Motor protein mutations cause a new form of hereditary spastic paraplegia by Caballero Oteyza, Andrés, Battaloğlu, Esra, Ocek, Levent, Lindig, Tobias, Reichbauer, Jennifer, Rebelo, Adriana P., Gonzalez, Michael A., Zorlu, Yasar, Ozes, Burcak, Timmann, Dagmar, Bender, Benjamin, Woehlke, Günther, Züchner, Stephan, Schöls, Ludger, Schüle, Rebecca
Published 2014Text -
14
What do we know about dynamic glucose-enhanced (DGE) MRI and how close is it to the clinics? Horizon 2020 GLINT consortium report by Kim, Mina, Eleftheriou, Afroditi, Ravotto, Luca, Weber, Bruno, Rivlin, Michal, Navon, Gil, Capozza, Martina, Anemone, Annasofia, Longo, Dario Livio, Aime, Silvio, Zaiss, Moritz, Herz, Kai, Deshmane, Anagha, Lindig, Tobias, Bender, Benjamin, Golay, Xavier
Published 2022Text -
15
Personalized neurorehabilitative precision medicine: from data to therapies (MWKNeuroReha) – a multi-centre prospective observational clinical trial to predict long-term outcome of... by Blum, Corinna, Baur, David, Achauer, Lars-Christian, Berens, Philipp, Biergans, Stephanie, Erb, Michael, Hömberg, Volker, Huang, Ziwei, Kohlbacher, Oliver, Liepert, Joachim, Lindig, Tobias, Lohmann, Gabriele, Macke, Jakob H., Römhild, Jörg, Rösinger-Hein, Christine, Zrenner, Brigitte, Ziemann, Ulf
Published 2022Text -
16
Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta by Garbes, Lutz, Kim, Kyungho, Rieß, Angelika, Hoyer-Kuhn, Heike, Beleggia, Filippo, Bevot, Andrea, Kim, Mi Jeong, Huh, Yang Hoon, Kweon, Hee-Seok, Savarirayan, Ravi, Amor, David, Kakadia, Purvi M., Lindig, Tobias, Kagan, Karl Oliver, Becker, Jutta, Boyadjiev, Simeon A., Wollnik, Bernd, Semler, Oliver, Bohlander, Stefan K., Kim, Jinoh, Netzer, Christian
Published 2015Text -
17
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications by Rattay, Tim W, Lindig, Tobias, Baets, Jonathan, Smets, Katrien, Deconinck, Tine, Söhn, Anne S, Hörtnagel, Konstanze, Eckstein, Kathrin N, Wiethoff, Sarah, Reichbauer, Jennifer, Döbler-Neumann, Marion, Krägeloh-Mann, Ingeborg, Auer-Grumbach, Michaela, Plecko, Barbara, Münchau, Alexander, Wilken, Bernd, Janauschek, Marc, Giese, Anne-Katrin, De Bleecker, Jan L, Ortibus, Els, Debyser, Martine, Lopez de Munain, Adolfo, Pujol, Aurora, Bassi, Maria Teresa, D’Angelo, Maria Grazia, De Jonghe, Peter, Züchner, Stephan, Bauer, Peter, Schöls, Ludger, Schüle, Rebecca
Published 2019Text -
18
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia by Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S, Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmüller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A, Stirnberg, Rüdiger, Sturm, Marc, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan, Heilmann-Heimbach, Stefanie, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Brüstle, Oliver, Klopstock, Thomas, Mathews, Katherine D, Shy, Michael E, de Jonghe, Peter, Chinnery, Patrick F, Horvath, Rita, Kohlhase, Jürgen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schöls, Ludger, Nürnberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo, Schüle, Rebecca
Published 2017Text