Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice
Bittner, R E, Schöfer, C, Weipoltshammer, K, Ivanova, S, Streubel, B, Hauser, E, Freilinger, M, Höger, H, Elbe-Bürger, A, Wachtler, F
Published in Anatomy and Embryology (01.05.1999)
Published in Anatomy and Embryology (01.05.1999)
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A novel de novo variant of GABRA1 causes increased sensitivity for GABA in vitro
Steudle, Friederike, Rehman, Sabah, Bampali, Konstantina, Simeone, Xenia, Rona, Zsofia, Hauser, Erwin, Schmidt, Wolfgang M, Scholze, Petra, Ernst, Margot
Published in Scientific reports (11.02.2020)
Published in Scientific reports (11.02.2020)
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5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2
Vill, Katharina, Tacke, Moritz, König, Anna, Baumann, Matthias, Baumgartner, Manuela, Steinbach, Meike, Bernert, Guenther, Blaschek, Astrid, Deschauer, Marcus, Flotats-Bastardas, Marina, Friese, Johannes, Goldbach, Susanne, Gross, Martin, Günther, René, Hahn, Andreas, Hagenacker, Tim, Hauser, Erwin, Horber, Veronka, Illsinger, Sabine, Johannsen, Jessika, Kamm, Christoph, Koch, Jan C., Koelbel, Heike, Koehler, Cornelia, Kolzter, Kirsten, Lochmüller, Hanns, Ludolph, Albert, Mensch, Alexander, Meyer zu Hoerste, Gerd, Mueller, Monika, Mueller-Felber, Wolfgang, Neuwirth, Christoph, Petri, Susanne, Probst-Schendzielorz, Kristina, Pühringer, Manuel, Steinbach, Robert, Schara-Schmidt, Ulrike, Schimmel, Mareike, Schrank, Bertold, Schwartz, Oliver, Schlachter, Kurt, Schwerin-Nagel, Annette, Schreiber, Gudrun, Smitka, Martin, Topakian, Raffi, Trollmann, Regina, Tuerk, Matthias, Theophil, Manuela, Rauscher, Christian, Vorgerd, Mathias, Walter, Maggie C., Weiler, Markus, Weiss, Claudia, Wilichowski, Ekkehard, Wurster, Claudia D., Wunderlich, Gilbert, Zeller, Daniel, Ziegler, Andreas, Kirschner, Janbernd, Pechmann, Astrid
Published in Journal of neurology (01.05.2024)
Published in Journal of neurology (01.05.2024)
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Long-term outcome and tolerability of the ketogenic diet in drug-resistant childhood epilepsy—The Austrian experience
Dressler, Anastasia, Stöcklin, Benjamin, Reithofer, Eva, Benninger, Franz, Freilinger, Michael, Hauser, Erwin, Reiter-Fink, Edith, Seidl, Rainer, Trimmel-Schwahofer, Petra, Feucht, Martha
Published in Seizure (London, England) (01.09.2010)
Published in Seizure (London, England) (01.09.2010)
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Behavioral and emotional problems in children with epilepsy
Freilinger, Michael, Reisel, Barbara, Reiter, Edith, Zelenko, Marina, Hauser, Erwin, Seidl, Rainer
Published in Journal of child neurology (01.11.2006)
Published in Journal of child neurology (01.11.2006)
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Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion
Denora, Paola S, Schlesinger, David, Casali, Carlo, Kok, Fernando, Tessa, Alessandra, Boukhris, Amir, Azzedine, Hamid, Dotti, Maria Teresa, Bruno, Claudio, Truchetto, Jeremy, Biancheri, Roberta, Fedirko, Estelle, Di Rocco, Maja, Bueno, Clarissa, Malandrini, Alessandro, Battini, Roberta, Sickl, Elisabeth, de Leva, Maria Fulvia, Boespflug-Tanguy, Odile, Silvestri, Gabriella, Simonati, Alessandro, Said, Edith, Ferbert, Andreas, Criscuolo, Chiara, Heinimann, Karl, Modoni, Anna, Weber, Peter, Palmeri, Silvia, Plasilova, Martina, Pauri, Flavia, Cassandrini, Denise, Battisti, Carla, Pini, Antonella, Tosetti, Michela, Hauser, Erwin, Masciullo, Marcella, Fabio, Roberto Di, Piccolo, Francesca, Denis, Elodie, Cioni, Giovanni, Massa, Roberto, Giustina, Elvio Della, Calabrese, Olga, Melone, Marina A.B, De Michele, Giuseppe, Federico, Antonio, Bertini, Enrico, Durr, Alexandra, Brockmann, Knut, van der Knaap, Marjo S, Zatz, Mayana, Filla, Alessandro, Brice, Alexis, Stevanin, Giovanni, Santorelli, Filippo M
Published in Human mutation (01.03.2009)
Published in Human mutation (01.03.2009)
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Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis
TILGEN, Nikola, ZORZATO, Francesco, TREVES, Susan, HALLIGER-KELLER, Birgit, MUNTONI, Francesco, SEWRY, Caroline, PALMUCCI, Laura M, SCHNEIDER, Christiane, HAUSER, Erwin, LEHMANN-HORN, Frank, MÜLLER, Clemens R
Published in Human molecular genetics (01.12.2001)
Published in Human molecular genetics (01.12.2001)
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Further evidence for the pathogenicity of 15q24 microduplications distal to the minimal critical regions
Roetzer, Katharina M., Schwarzbraun, Thomas, Obenauf, Anna C., Hauser, Erwin, Speicher, Michael R.
Published in American journal of medical genetics. Part A (01.12.2010)
Published in American journal of medical genetics. Part A (01.12.2010)
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Vacuum pump system with wireless remote control
Hauser, Erwin, Roth, Uwe
Published in Vakuum in Forschung und Praxis : Zeitschrift für Vakuumtechnologie, Oberflèachen und Dünne Schichten (01.04.2009)
Published in Vakuum in Forschung und Praxis : Zeitschrift für Vakuumtechnologie, Oberflèachen und Dünne Schichten (01.04.2009)
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4G/5G promoter polymorphism in the plasminogen-activator-inhibitor-1 gene in children with systemic meningococcaemia
GEISHOFER, Gotho, BINDER, Alexander, ZENZ, Werner, MÜLLER, Martin, ZÖHRER, Bettina, RESCH, Bernhard, MÜLLER, Wilhelm, FABER, Jörg, FINN, Adam, ENDLER, Georg, MANNHALTER, Christine
Published in European journal of pediatrics (01.08.2005)
Published in European journal of pediatrics (01.08.2005)
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