Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rosa, Weng"'
Autor:
Verena Endmayr, Cansu Tunc, Lara Ergin, Anna De Rosa, Rosa Weng, Lukas Wagner, Thin-Yau Yu, Andreas Fichtenbaum, Thomas Perkmann, Helmuth Haslacher, Nicolas Kozakowski, Carmen Schwaiger, Gerda Ricken, Simon Hametner, Sigrid Klotz, Lívia Almeida Dutra, Christian Lechner, Désirée de Simoni, Kai-Nicolas Poppert, Georg Johannes Müller, Susanne Pirker, Walter Pirker, Aleksandra Angelovski, Matus Valach, Michelangelo Maestri, Melania Guida, Roberta Ricciardi, Florian Frommlet, Daniela Sieghart, Miklos Pinter, Karl Kircher, Gottfried Artacker, Romana Höftberger, Inga Koneczny
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
BackgroundIgG4 is associated with two emerging groups of rare diseases: 1) IgG4 autoimmune diseases (IgG4-AID) and 2) IgG4-related diseases (IgG4-RLD). Anti-neuronal IgG4-AID include MuSK myasthenia gravis, LGI1- and Caspr2-encephalitis and autoimmun
Externí odkaz:
https://doaj.org/article/52df9cde5bcf4c4991369c2ebf5cf182
Autor:
Rosa Weng, Karl-Heinz Nenning, Michelle Schwarz, Korbinian M. Riedhammer, Theresa Brunet, Matias Wagner, Gregor Kasprian, Johann Lehrner, Fritz Zimprich, Silvia B. Bonelli, Martin Krenn
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 43:e419-e422
Causative variants in SETD1B , encoding a lysine-specific methyltransferase, have recently been associated with a neurodevelopmental phenotype encompassing intellectual disability, autistic features, pronounced language delay, and epilepsy. It has be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed8139b1bf9f2b6e2733008b6ab19a98
https://doi.org/10.1097/dbp.0000000000001079
https://doi.org/10.1097/dbp.0000000000001079
Autor:
Martin Krenn, Matthias Tomschik, Matias Wagner, Gudrun Zulehner, Rosa Weng, Jakob Rath, Sigrid Klotz, Ellen Gelpi, Gabriel Bsteh, Omar Keritam, Isabella Colonna, Chiara Paternostro, Fiona Jäger, Elisabeth Lindeck‐Pozza, Stephan Iglseder, Susanne Grinzinger, Martina Schönfelder, Christina Hohenwarter, Manfred Freimüller, Norbert Embacher, Julia Wanschitz, Raffi Topakian, Ana Töpf, Volker Straub, Stefan Quasthoff, Fritz Zimprich, Wolfgang N. Löscher, Hakan Cetin
Publikováno v:
Eur. J. Neurol. 29, 1815-1824 (2022)
Hereditary myopathies with limb-girdle muscular weakness (LGW) are a genetically heterogeneous group of disorders, in which molecular diagnosis remains challenging. Our aim was to present a detailed clinical and genetic characterization of a large co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d69fd628f4b40ca99a78490f29f9ef5c
https://doi.org/10.1111/ene.15306
https://doi.org/10.1111/ene.15306
Incidence and clinical spectrum of rhabdomyolysis in general neurology: a retrospective cohort study
Autor:
Jakob Rath, Karl Bointner, Hakan Cetin, Rosa Weng, Lorina Gopp, Fiona Jäger, Thomas Berger, Fritz Zimprich, Chiara Paternostro, Martin Krenn, Gudrun Zulehner, Matthias Tomschik
Publikováno v:
Neuromuscular Disorders. 31:1227-1234
The objective of this retrospective cohort study was to evaluate demographic, clinical and laboratory characteristics of patients with rhabdomyolysis as defined by a serum creatine kinase (sCK) activity > 950 U/L. A total of 248 patients were recruit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::415ee5799d0357c8f86ce3dd0e3aa2b5
https://doi.org/10.1016/j.nmd.2021.09.012
https://doi.org/10.1016/j.nmd.2021.09.012
Autor:
Georg Scheriau, Rosa Weng, Andrea Lassnigg, Mathias Maleczek, Fritz Zimprich, Jose Matilla, Bernhard Moser, Martin H. Bernardi
Publikováno v:
Journal of cardiothoracic and vascular anesthesia. 36(10)
Postoperative myasthenic crisis with respiratory failure is a potentially lethal complication, warranting careful perioperative planning and extended postoperative surveillance of patients. Data on the incidence of postoperative respiratory failure a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c097a793be19af621d227888ccfdf0dd
https://pubmed.ncbi.nlm.nih.gov/35871043
https://pubmed.ncbi.nlm.nih.gov/35871043
Autor:
Verena, Endmayr, Cansu, Tunc, Lara, Ergin, Anna, De Rosa, Rosa, Weng, Lukas, Wagner, Thin-Yau, Yu, Andreas, Fichtenbaum, Thomas, Perkmann, Helmuth, Haslacher, Nicolas, Kozakowski, Carmen, Schwaiger, Gerda, Ricken, Simon, Hametner, Sigrid, Klotz, Lívia Almeida, Dutra, Christian, Lechner, Désirée, de Simoni, Kai-Nicolas, Poppert, Georg Johannes, Müller, Susanne, Pirker, Walter, Pirker, Aleksandra, Angelovski, Matus, Valach, Michelangelo, Maestri, Melania, Guida, Roberta, Ricciardi, Florian, Frommlet, Daniela, Sieghart, Miklos, Pinter, Karl, Kircher, Gottfried, Artacker, Romana, Höftberger, Inga, Koneczny
Publikováno v:
Frontiers in Immunology
Background IgG4 is associated with two emerging groups of rare diseases: 1) IgG4 autoimmune diseases (IgG4-AID) and 2) IgG4-related diseases (IgG4-RLD). Anti-neuronal IgG4-AID include MuSK myasthenia gravis, LGI1- and Caspr2-encephalitis and autoimmu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6632aed4f108e691a24834d2fdda217
https://pubmed.ncbi.nlm.nih.gov/35095860
https://pubmed.ncbi.nlm.nih.gov/35095860