Resultados da busca - Klebe, Stephan

Tiefe Hirnstimulation bei neurologischen und psychiatrischen Erkrankungen por Klebe, Stephan, Coenen, Volker

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SARS-CoV-2, COVID-19 and Neurodegeneration por Tönges, Lars, Klebe, Stephan

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Monogenetic Forms of Parkinson’s Disease – Bridging the Gap Between Genetics and Biomarkers por Tönges, Lars, Kwon, Eun Hae, Klebe, Stephan

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Anti-GFAP-antibody positive postinfectious acute cerebellar ataxia and myoclonus after COVID-19: a case report por Asan, Livia, Klebe, Stephan, Kleinschnitz, Christoph, Stettner, Mark, Köhrmann, Martin

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SARS-CoV-2, COVID-19 and Parkinson’s Disease—Many Issues Need to Be Clarified—A Critical Review por Goerttler, Tsepo, Kwon, Eun-Hae, Fleischer, Michael, Stettner, Mark, Tönges, Lars, Klebe, Stephan

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Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP) por Karle, Kathrin N, Schüle, Rebecca, Klebe, Stephan, Otto, Susanne, Frischholz, Christian, Liepelt-Scarfone, Inga, Schöls, Ludger

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Ataxia and autonomic dysfunction as presenting symptoms in late-onset Alexander disease por Jost, Meike, Rijntjes, Michel, Urbach, Horst, Egger, Karl, Meyer, Philipp T., Frings, Lars, Weiller, Cornelius, Klebe, Stephan

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Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation por Weber, Juliane, Frings, Lars, Rijntjes, Michel, Urbach, Horst, Fischer, Judith, Weiller, Cornelius, Meyer, Philipp T., Klebe, Stephan

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Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult por Piroth, Tobias, Boelmans, Kai, Amtage, Florian, Rijntjes, Michel, Wierciochin, Anna, Musacchio, Thomas, Weiller, Cornelius, Volkmann, Jens, Klebe, Stephan

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Atypical Presentation of Rapid‐onset Dystonia‐parkinsonism (DYT12) Unresponsive to Deep Brain Stimulation of the Subthalamic Nucleus por Weber, Juliane, Piroth, Tobias, Rijntjes, Michel, Jung, Bernhard, Reinacher, Peter C., Weiller, Cornelius, Coenen, Volker A., Klebe, Stephan

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Adult-Onset Alexander Disease: New Causal Sequence Variant in the GFAP Gene por Goerttler, Tsepo, Zanetti, Letizia, Regoni, Maria, Egger, Karl, Kellner, Elias, Deuschl, Cornelius, Kleinschnitz, Christoph, Sassone, Jenny, Klebe, Stephan

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Reply: Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers por Mencacci, Niccolo E., Pittman, Alan M., Isaias, Ioannis U., Hardy, John, Klebe, Stephan, Bhatia, Kailash P., Wood, Nicholas W.

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Non-Motor Symptoms of Essential Tremor Are Independent of Tremor Severity and Have an Impact on Quality of Life por Musacchio, Thomas, Purrer, Veronika, Papagianni, Aikaterini, Fleischer, Anna, Mackenrodt, Daniel, Malsch, Carolin, Gelbrich, Götz, Steigerwald, Frank, Volkmann, Jens, Klebe, Stephan

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Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients por Lorenz, Delia, Klebe, Stephan, Stevanin, Giovanni, Thier, Sandra, Nebel, Almut, Feingold, Josué, Frederiksen, Henrik, Denis, Elodie, Christensen, Kaare, Schreiber, Stefan, Brice, Alexis, Deuschl, Günther, Dürr, Alexandra

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TDP‐43 as structure‐based biomarker in amyotrophic lateral sclerosis por Beyer, Léon, Günther, René, Koch, Jan Christoph, Klebe, Stephan, Hagenacker, Tim, Lingor, Paul, Biesalski, Anne‐Sophie, Hermann, Andreas, Nabers, Andreas, Gold, Ralf, Tönges, Lars, Gerwert, Klaus

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Resource Utilization of Patients with Parkinson’s Disease in the Late Stages of the Disease in Germany: Data from the CLaSP Study por Kruse, Christopher, Kretschmer, Sabrina, Lipinski, Anna, Verheyen, Malte, Mengel, David, Balzer-Geldsetzer, Monika, Lorenzl, Stefan, Richinger, Carmen, Schmotz, Christian, Tönges, Lars, Woitalla, Dirk, Klebe, Stephan, Schrag, Anette, Dodel, Richard

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Dermal phospho-alpha-synuclein deposits confirm REM sleep behaviour disorder as prodromal Parkinson’s disease por Doppler, Kathrin, Jentschke, Hanna-Maria, Schulmeyer, Lena, Vadasz, David, Janzen, Annette, Luster, Markus, Höffken, Helmut, Mayer, Geert, Brumberg, Joachim, Booij, Jan, Musacchio, Thomas, Klebe, Stephan, Sittig-Wiegand, Elisabeth, Volkmann, Jens, Sommer, Claudia, Oertel, Wolfgang H.

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A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) por Schlipf, Nina A, Beetz, Christian, Schüle, Rebecca, Stevanin, Giovanni, Erichsen, Anne Kjersti, Forlani, Sylvie, Zaros, Cécile, Karle, Kathrin, Klebe, Stephan, Klimpe, Sven, Durr, Alexandra, Otto, Susanne, Tallaksen, Chantal M E, Riess, Olaf, Brice, Alexis, Bauer, Peter, Schöls, Ludger

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Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor por Thier, Sandra, Lorenz, Delia, Nothnagel, Michael, Poremba, Caroline, Papengut, Frank, Appenzeller, Silke, Paschen, Steffen, Hofschulte, Frank, Hussl, Anna-Christina, Hering, Sascha, Poewe, Werner, Asmus, Friedrich, Gasser, Thomas, Schöls, Ludger, Christensen, Kaare, Nebel, Almut, Schreiber, Stefan, Klebe, Stephan, Deuschl, Günther, Kuhlenbäumer, Gregor

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations por Klebe, Stephan, Lossos, Alexander, Azzedine, Hamid, Mundwiller, Emeline, Sheffer, Ruth, Gaussen, Marion, Marelli, Cecilia, Nawara, Magdalena, Carpentier, Wassila, Meyer, Vincent, Rastetter, Agnès, Martin, Elodie, Bouteiller, Delphine, Orlando, Laurent, Gyapay, Gabor, El-Hachimi, Khalid H, Zimmerman, Batel, Gamliel, Moriya, Misk, Adel, Lerer, Israela, Brice, Alexis, Durr, Alexandra, Stevanin, Giovanni

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