检索结果 - Klebe, Stephan

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

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

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Monogenetic Forms of Parkinson’s Disease – Bridging the Gap Between Genetics and Biomarkers 由 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 由 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 由 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) 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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) 由 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 由 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 由 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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