Arama Sonuçları - Minnerop, Martina

Current Progress in CNS Imaging of Myotonic Dystrophy Yazar: Minnerop, Martina, Gliem, Carla, Kornblum, Cornelia

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Cytoarchitectonic mapping of the human brain cerebellar nuclei in stereotaxic space and delineation of their co-activation patterns Yazar: Tellmann, Stefanie, Bludau, Sebastian, Eickhoff, Simon, Mohlberg, Hartmut, Minnerop, Martina, Amunts, Katrin

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Dual task effect on postural control in patients with degenerative cerebellar disorders Yazar: Jacobi, Heike, Alfes, Juliane, Minnerop, Martina, Konczak, Jürgen, Klockgether, Thomas, Timmann, Dagmar

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Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2 Yazar: Bernard, Veronica, Minnerop, Martina, Bürk, Katrin, Kreuz, Friedmar, Gillessen-Kaesbach, Gabriele, Zühlke, Christine

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Neuropsychological Features of Patients with Spinocerebellar Ataxia (SCA) Types 1, 2, 3, and 6 Yazar: Klinke, Ina, Minnerop, Martina, Schmitz-Hübsch, Tanja, Hendriks, Marc, Klockgether, Thomas, Wüllner, Ullrich, Helmstaedter, Christoph

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System Comparison for Gait and Balance Monitoring Used for the Evaluation of a Home-Based Training Yazar: Rentz, Clara, Far, Mehran Sahandi, Boltes, Maik, Schnitzler, Alfons, Amunts, Katrin, Dukart, Juergen, Minnerop, Martina

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Derivation of Fiber Orientations From Oblique Views Through Human Brain Sections in 3D-Polarized Light Imaging Yazar: Schmitz, Daniel, Muenzing, Sascha E. A., Schober, Martin, Schubert, Nicole, Minnerop, Martina, Lippert, Thomas, Amunts, Katrin, Axer, Markus

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Reply: POLR3A variants in hereditary spastic paraplegia and ataxia Yazar: Minnerop, Martina, Kurzwelly, Delia, Rattay, Tim W, Timmann, Dagmar, Hengel, Holger, Synofzik, Matthis, Stendel, Claudia, Horvath, Rita, Schüle, Rebecca, Ramirez, Alfredo

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Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich’s ataxia Yazar: Stefanescu, Maria R., Dohnalek, Moritz, Maderwald, Stefan, Thürling, Markus, Minnerop, Martina, Beck, Andreas, Schlamann, Marc, Diedrichsen, Joern, Ladd, Mark E., Timmann, Dagmar

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Grey and white matter loss along cerebral midline structures in myotonic dystrophy type 2 Yazar: Minnerop, Martina, Luders, Eileen, Specht, Karsten, Ruhlmann, Jürgen, Schneider-Gold, Christiane, Schröder, Rolf, Thompson, Paul M., Toga, Arthur W., Klockgether, Thomas, Kornblum, Cornelia

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Neurochemical Differences in Spinocerebellar Ataxia Type 14 and 1 Yazar: Grosch, Anne Sophie, Rinnenthal, Jan Leo, Rönnefarth, Maria, Lux, Silke, Scheel, Michael, Endres, Matthias, Brandt, Alexander U., Paul, Friedemann, Schmitz-Hübsch, Tanja, Minnerop, Martina, Doss, Sarah

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The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease Yazar: Minnerop, Martina, Weber, Bernd, Schoene-Bake, Jan-Christoph, Roeske, Sandra, Mirbach, Sandra, Anspach, Christian, Schneider-Gold, Christiane, Betz, Regina C., Helmstaedter, Christoph, Tittgemeyer, Marc, Klockgether, Thomas, Kornblum, Cornelia

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Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14 Yazar: Ihl, Thomas, Kadas, Ella M., Oberwahrenbrock, Timm, Endres, Matthias, Klockgether, Thomas, Schroeter, Jan, Brandt, Alexander U., Paul, Friedemann, Minnerop, Martina, Doss, Sarah, Schmitz-Hübsch, Tanja, Zimmermann, Hanna G.

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Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias Yazar: Deistung, Andreas, Jäschke, Dominik, Draganova, Rossitza, Pfaffenrot, Viktor, Hulst, Thomas, Steiner, Katharina M., Thieme, Andreas, Giordano, Ilaria A., Klockgether, Thomas, Tunc, Sinem, Münchau, Alexander, Minnerop, Martina, Göricke, Sophia L., Reichenbach, Jürgen R., Timmann, Dagmar

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Tracking the brain in myotonic dystrophies: A 5-year longitudinal follow-up study Yazar: Gliem, Carla, Minnerop, Martina, Roeske, Sandra, Gärtner, Hanna, Schoene-Bake, Jan-Christoph, Adler, Sandra, Witt, Juri-Alexander, Hoffstaedter, Felix, Schneider-Gold, Christiane, Betz, Regina C., Helmstaedter, Christoph, Tittgemeyer, Marc, Amunts, Katrin, Klockgether, Thomas, Weber, Bernd, Kornblum, Cornelia

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Validation of a German version of the Cerebellar Cognitive Affective/ Schmahmann Syndrome Scale: preliminary version and study protocol Yazar: Thieme, Andreas, Roeske, Sandra, Faber, Jennifer, Sulzer, Patricia, Minnerop, Martina, Elben, Saskia, Jacobi, Heike, Reetz, Kathrin, Dogan, Imis, Barkhoff, Miriam, Konczak, Juergen, Wondzinski, Elke, Siebler, Mario, Mueller, Oliver, Sure, Ulrich, Schmahmann, Jeremy D., Klockgether, Thomas, Synofzik, Matthis, Timmann, Dagmar

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The CCAS-scale in hereditary ataxias: helpful on the group level, particularly in SCA3, but limited in individual patients Yazar: Thieme, Andreas, Faber, Jennifer, Sulzer, Patricia, Reetz, Kathrin, Dogan, Imis, Barkhoff, Miriam, Krahe, Janna, Jacobi, Heike, Aktories, Julia-Elisabeth, Minnerop, Martina, Elben, Saskia, van der Veen, Raquel, Müller, Johanna, Batsikadze, Giorgi, Konczak, Jürgen, Synofzik, Matthis, Roeske, Sandra, Timmann, Dagmar

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Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS Yazar: Caspers, Svenja, Moebus, Susanne, Lux, Silke, Pundt, Noreen, Schütz, Holger, Mühleisen, Thomas W., Gras, Vincent, Eickhoff, Simon B., Romanzetti, Sandro, Stöcker, Tony, Stirnberg, Rüdiger, Kirlangic, Mehmet E., Minnerop, Martina, Pieperhoff, Peter, Mödder, Ulrich, Das, Samir, Evans, Alan C., Jöckel, Karl-Heinz, Erbel, Raimund, Cichon, Sven, Nöthen, Markus M., Sturma, Dieter, Bauer, Andreas, Jon Shah, N., Zilles, Karl, Amunts, Katrin

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Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult‐onset disorder Yazar: Schmitz‐Hübsch, Tanja, Lux, Silke, Bauer, Peter, Brandt, Alexander U., Schlapakow, Elena, Greschus, Susanne, Scheel, Michael, Gärtner, Hanna, Kirlangic, Mehmet E., Gras, Vincent, Timmann, Dagmar, Synofzik, Matthis, Giorgetti, Alejandro, Carloni, Paolo, Shah, Jon N., Schöls, Ludger, Kopp, Ute, Bußenius, Lisa, Oberwahrenbrock, Timm, Zimmermann, Hanna, Pfueller, Caspar, Kadas, Ella‐Maria, Rönnefarth, Maria, Grosch, Anne‐Sophie, Endres, Matthias, Amunts, Katrin, Paul, Friedemann, Doss, Sarah, Minnerop, Martina

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The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias Yazar: Traschütz, Andreas, Reich, Selina, Adarmes, Astrid D., Anheim, Mathieu, Ashrafi, Mahmoud Reza, Baets, Jonathan, Basak, A. Nazli, Bertini, Enrico, Brais, Bernard, Gagnon, Cynthia, Gburek-Augustat, Janina, Hanagasi, Hasmet A., Heinzmann, Anna, Horvath, Rita, de Jonghe, Peter, Kamm, Christoph, Klivenyi, Peter, Klopstock, Thomas, Minnerop, Martina, Münchau, Alexander, Renaud, Mathilde, Roxburgh, Richard H., Santorelli, Filippo M., Schirinzi, Tommaso, Sival, Deborah A., Timmann, Dagmar, Vielhaber, Stefan, Wallner, Michael, van de Warrenburg, Bart P., Zanni, Ginevra, Zuchner, Stephan, Klockgether, Thomas, Schüle, Rebecca, Schöls, Ludger, Synofzik, Matthis

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