Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Philipp Simschitz"'
Autor:
Fahmy Aboul-Enein, Thomas Seifert-Held, Simone Mader, Bettina Kuenz, Andreas Lutterotti, Helmut Rauschka, Paulus Rommer, Fritz Leutmezer, Karl Vass, Agathe Flamm-Horak, Robert Stepansky, Wilfried Lang, Elisabeth Fertl, Thomas Schlager, Thomas Heller, Christian Eggers, Georg Safoschnik, Siegrid Fuchs, Jörg Kraus, Hamid Assar, Stefan Guggenberger, Martin Reisz, Peter Schnabl, Martina Komposch, Philipp Simschitz, Alena Skrobal, Alexander Moser, Mario Jeschow, Dorothea Stadlbauer, Manfred Freimüller, Michael Guger, Susanne Schmidegg, Claudia Franta, Vera Weiser, Stefan Koppi, Margret Niederkorn-Duft, Bettina Raber, Iris Schmeissner, Julia Jecel, Alexander Tinchon, Maria K Storch, Markus Reindl, Thomas Berger, Wolfgang Kristoferitsch
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79649 (2013)
BackgroundIn 2008 the Austrian Task Force for Neuromyelitis Optica (NMO) started a nation-wide network for information exchange and multi-centre collaboration. Their aim was to detect all patients with NMO or NMO spectrum disorders (NMO-SD) in Austri
Externí odkaz:
https://doaj.org/article/5efd90c6d18646beb630349dd1ca3dde
Autor:
Christian Eggers, Florian B. Lagler, Stefan Quasthoff, Wolfgang Löscher, Stephan Iglseder, Philipp Simschitz, S. Grinzinger, Reginald E. Bittner, Wolfgang M. Schmidt, U. Lex, Michael Freilinger, Dorothea Möslinger, H. Moser, Michaela Brunner-Krainz, Thomas M. Stulnig, M. Reichhardt, Julia Wanschitz, M. Huemer
Publikováno v:
Journal of Neurology
In this study, we performed a survey of infantile and late-onset Pompe disease (IOPD and LOPD) in Austria. Paediatric and neuromuscular centres were contacted to provide a set of anonymized clinical and genetic data of patients with IOPD and LOPD. Th
Autor:
Martina Komposch, Claudia Franta, Helmut Rauschka, Johann Sellner, Hans Offenbacher, Franz Fazekas, Barbara Teuchner, Ferdinand Otto, Philipp Simschitz, Beate J Langner-Wegscheider, Thomas Seifert-Held
Publikováno v:
International Journal of Neuroscience. 127:776-780
Susac's syndrome is characterized by inflammation and occlusion of pre-capillary arterioles with the clinical triad of branch retinal artery occlusion (BRAO), encephalopathy and hearing loss. No epidemiological data are available for the disease.All
Autor:
Dierk Oel, Raffi Topakian, Karl Stieglbauer, Jakob Rath, Wolfgang Löscher, Michael Guger, Stefan Einsiedler, Petra Müller, Philipp Simschitz, Günther Schustereder, Julia Wanschitz, Norbert Embacher, Stephan Iglseder, David Windisch, Dieter Langenscheidt, Christian Eggers, Fritz Zimprich, Stefan Quasthoff
Publikováno v:
Journal of neurology. 266(3)
Most patients with myasthenia gravis (MG) need long-term immunosuppressive therapy. However, conventional agents may have intolerable side effects, take too long or fail to achieve disease control. Rituximab (RTX) has emerged as an off-label treatmen
Autor:
Peter Schnabl, Martina Komposch, Thomas Berger, Maria K. Storch, Georg Safoschnik, Manfred Freimüller, Margret Niederkorn-Duft, Wilfried Lang, Thomas Schlager, Bettina Raber, Vera Weiser, Alena Skrobal, Mario Jeschow, Christian Eggers, Andreas Lutterotti, Wolfgang Kristoferitsch, Agathe Flamm-Horak, Helmut Rauschka, Simone Mader, Philipp Simschitz, Fahmy Aboul-Enein, Robert Stepansky, Susanne Schmidegg, Alexander Moser, Dorothea Stadlbauer, Bettina Kuenz, Paulus S. Rommer, Elisabeth Fertl, Claudia Franta, Stefan Koppi, Martin Reisz, Fritz Leutmezer, Iris Schmeissner, Hamid Assar, Michael Guger, Stefan Guggenberger, Thomas Heller, Thomas Seifert-Held, Alexander Tinchon, Markus Reindl, Jörg Kraus, Siegrid Fuchs, Karl Vass, Julia Jecel
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 11, p e79649 (2013)
PLoS ONE, Vol 8, Iss 11, p e79649 (2013)
BackgroundIn 2008 the Austrian Task Force for Neuromyelitis Optica (NMO) started a nation-wide network for information exchange and multi-centre collaboration. Their aim was to detect all patients with NMO or NMO spectrum disorders (NMO-SD) in Austri