Результаты поиска - Lindig, Tobias
- Отображение 1 - 18 результаты of 18
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Encephalopathic Susac’s Syndrome associated with livedo racemosa in a young woman before the completion of family planning по Engeholm, Maik, Leo-Kottler, Beate, Rempp, Hansjörg, Lindig, Tobias, Lerche, Holger, Kleffner, Ilka, Henes, Melanie, Dihné, Marcel
Опубликовано 2013Текст -
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GLINT: GlucoCEST in neoplastic tumors at 3 T—clinical results of GlucoCEST in gliomas по 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
Опубликовано 2021Текст -
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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 по 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
Опубликовано 2014Текст -
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White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease по 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
Опубликовано 2017Текст -
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Corrigendum: White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease по 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
Опубликовано 2017Текст -
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Motor protein mutations cause a new form of hereditary spastic paraplegia по 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
Опубликовано 2014Текст -
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What do we know about dynamic glucose-enhanced (DGE) MRI and how close is it to the clinics? Horizon 2020 GLINT consortium report по 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
Опубликовано 2022Текст -
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Personalized neurorehabilitative precision medicine: from data to therapies (MWKNeuroReha) – a multi-centre prospective observational clinical trial to predict long-term outcome of... по 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
Опубликовано 2022Текст -
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Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta по 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
Опубликовано 2015Текст -
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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications по 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
Опубликовано 2019Текст -
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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia по 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
Опубликовано 2017Текст