Výsledky vyhledávání - Lindig, Tobias
- Zobrazuji výsledky 1 - 18 z 18
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Ammonia and coma – a case report of late onset hemizygous ornithine carbamyltransferase deficiency in 68-year-old female Autor Marquetand, Justus, Freisinger, Peter, Lindig, Tobias, Euler, Sebastian, Gasser, Michael, Overkamp, Dietrich
Vydáno 2020Text -
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Encephalopathic Susac’s Syndrome associated with livedo racemosa in a young woman before the completion of family planning Autor Engeholm, Maik, Leo-Kottler, Beate, Rempp, Hansjörg, Lindig, Tobias, Lerche, Holger, Kleffner, Ilka, Henes, Melanie, Dihné, Marcel
Vydáno 2013Text -
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3D gradient echo snapshot CEST MRI with low power saturation for human studies at 3T Autor Deshmane, Anagha, Zaiss, Moritz, Lindig, Tobias, Herz, Kai, Schuppert, Mark, Gandhi, Chirayu, Bender, Benjamin, Ernemann, Ulrike, Scheffler, Klaus
Vydáno 2018Text -
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GLINT: GlucoCEST in neoplastic tumors at 3 T—clinical results of GlucoCEST in gliomas Autor 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
Vydáno 2021Text -
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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 Autor 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
Vydáno 2014Text -
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White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease Autor 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
Vydáno 2017Text -
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Corrigendum: White Matter Changes-Related Gait and Executive Function Deficits: Associations with Age and Parkinson's Disease Autor 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
Vydáno 2017Text -
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Motor protein mutations cause a new form of hereditary spastic paraplegia Autor 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
Vydáno 2014Text -
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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 Autor 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
Vydáno 2022Text -
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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... Autor 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
Vydáno 2022Text -
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Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta Autor 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
Vydáno 2015Text -
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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications Autor 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
Vydáno 2019Text -
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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia Autor 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
Vydáno 2017Text