Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients von Schüle, Rebecca, Wiethoff, Sarah, Martus, Peter, Karle, Kathrin N., Otto, Susanne, Klebe, Stephan, Klimpe, Sven, Gallenmüller, Constanze, Kurzwelly, Delia, Henkel, Dorothea, Rimmele, Florian, Stolze, Henning, Kohl, Zacharias, Kassubek, Jan, Klockgether, Thomas, Vielhaber, Stefan, Kamm, Christoph, Klopstock, Thomas, Bauer, Peter, Züchner, Stephan, Liepelt-Scarfone, Inga, Schöls, Ludger

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Distinctive distribution of phospho-alpha-synuclein in dermal nerves in multiple system atrophy von Doppler, Kathrin, Weis, Jessica, Karl, Katharina, Ebert, Sönke, Ebentheuer, Jens, Trenkwalder, Claudia, Klebe, Stephan, Volkmann, Jens, Sommer, Claudia

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Monogenetic Forms of Parkinson's Disease - Bridging the Gap Between Genetics and Biomarkers von Tönges, Lars, Kwon, Eun Hae, Klebe, Stephan

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

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Clinically approved immunomodulators ameliorate behavioral changes in a mouse model of hereditary spastic paraplegia type 11 von Hörner, Michaela, Popp, Sandy, Branchu, Julien, Stevanin, Giovanni, Darios, Frédéric, Klebe, Stephan, Groh, Janos, Martini, Rudolf

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Development and validation of TreatHSP-QoL: a patient-reported outcome measure for health-related quality of life in hereditary spastic paraplegia von Malina, Jekaterina, Huessler, Eva-Maria, Jöckel, Karl-Heinz, Boog-Whiteside, Eva, Jeschonneck, Nicole, Schröder, Bernadette, Schüle, Rebecca, Kühl, Tobias, Klebe, Stephan

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Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal Study von Lee, Pei‐Chen, Artaud, Fanny, Cormier‐Dequaire, Florence, Rascol, Olivier, Durif, Franck, Derkinderen, Pascal, Marques, Ana‐Raquel, Bourdain, Frédéric, Brandel, Jean‐Philippe, Pico, Fernando, Lacomblez, Lucette, Bonnet, Cecilia, Brefel‐Courbon, Christine, Ory‐Magne, Fabienne, Grabli, David, Klebe, Stephan, Mangone, Graziella, You, Hana, Mesnage, Valérie, Brice, Alexis, Vidailhet, Marie, Corvol, Jean‐Christophe, Elbaz, Alexis

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Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions von Mohren, Lars, Erdlenbruch, Friedrich, Leitão, Elsa, Kilpert, Fabian, Hönes, G. Sebastian, Kaya, Sabine, Schröder, Christopher, Thieme, Andreas, Sturm, Marc, Park, Joohyun, Schlüter, Agatha, Ruiz, Montserrat, Morales de la Prida, Moisés, Casasnovas, Carlos, Becker, Kerstin, Roggenbuck, Ulla, Pechlivanis, Sonali, Kaiser, Frank J., Synofzik, Matthis, Wirth, Thomas, Anheim, Mathieu, Haack, Tobias B., Lockhart, Paul J., Jöckel, Karl-Heinz, Pujol, Aurora, Klebe, Stephan, Timmann, Dagmar, Depienne, Christel

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations von KLEBEL, Stephan, LOSSOS, Alexander, RASTETTER, Agnes, MARTIN, Elodie, BOUTEILLER, Delphine, ORLANDO, Laurent, GYAPAY, Gabor, EL-HACHIMI, Khalid H, ZIMMERMAN, Batel, GAMLIEL, Moriya, MISK, Adel, LERER, Israela, AZZEDINE, Hamid, BRICE, Alexis, DURR, Alexandra, STEVANIN, Giovanni, MUNDWILLER, Emeline, SHEFFER, Ruth, GAUSSEN, Marion, MARELLI, Cecilia, NAWARA, Magdalena, CARPENTIER, Wassila, MEYER, Vincent

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Anti-GFAP-antibody positive postinfectious acute cerebellar ataxia and myoclonus after COVID-19: a case report von 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 von Goerttler, Tsepo, Kwon, Eun-Hae, Fleischer, Michael, Stettner, Mark, Tönges, Lars, Klebe, Stephan

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Iatrogenic botulism after intragastric botulinum neurotoxin injections - a major outbreak von Goerttler, Tsepo, Dorner, Martin B, van der Linden, Christina, Kienitz, Ricardo, Petrik, Stephan, Blechinger, Stephan, Spickschen, Jonah, Betz, Iris R, Hinrichs, Carl, Steindl, David, Weber, Frederike, Musacchio, Thomas, Wunderlich, Gilbert, Rueger, Maria Adele, Barbe, Michael T, Dafsari, Haidar, Demir, Seda, Lapa, Sriramya, Zeiner, Pia S, Strzelczyk, Adam, Tinnemann, Peter, Kleine, Christian, Totzeck, Andreas, Klebe, Stephan, Mikolajewska, Agata, Dorner, Brigitte G, Fertl, Elisabeth, Grefkes-Hermann, Christian, Fink, Gereon, Kleinschnitz, Christoph, Hagenacker, Tim

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

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Deep brain stimulation in neurological and psychiatric diseases von Klebe, Stephan, Coenen, Volker

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Prevalence of gait disorders in hospitalized neurological patients von Stolze, Henning, Klebe, Stephan, Baecker, Christoph, Zechlin, Christiane, Friege, Lars, Pohle, Sabine, Deuschl, Günther

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

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Genetics of movement disorders-rare but important von Klebe, Stephan, Timmann, Dagmar

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Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting von Klebe, S., Stevanin, G., Depienne, C.

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

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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) von Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni

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