Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Omar Keritam"'
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The discovery of autoantibodies directed against muscle-specific kinase (MuSK) in “seronegative” myasthenia gravis (MG) patients marked a milestone in MG research. In healthy muscle, MuSK regulates a phosphorylation pathway, which is essential fo
Externí odkaz:
https://doaj.org/article/52c1ca63120c45dda5b9d36536fcee5f
Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation
Autor:
Tandis Parvizi, Sigrid Klotz, Omar Keritam, Haluk Caliskan, Sophie Imhof, Theresa König, Lukas Haider, Tatjana Traub‐Weidinger, Matias Wagner, Theresa Brunet, Melanie Brugger, Alexander Zimprich, Jakob Rath, Elisabeth Stögmann, Ellen Gelpi, Hakan Cetin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 6, Pp 1579-1589 (2024)
Abstract Objective Mutations in the gene encoding for optineurin (OPTN) have been reported in the context of different neurodegenerative diseases including the amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) spectrum. Based on s
Externí odkaz:
https://doaj.org/article/3c6d0f0f683f471fbf37374686e34d4b
Autor:
Omar Keritam, Viktoria Juhasz, Christian Schöfer, Christiane Thallinger, Marie-Bernadette Aretin, Gernot Schabbauer, Johannes Breuss, Matthias Unseld, Pavel Uhrin
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Background: Extravasation during chemotherapy administration can lead to dangerous adverse effects ranging from pain to tissue necrosis. Evidence-based data about prevention and treatment of extravasation injuries of some clinically used compounds st
Externí odkaz:
https://doaj.org/article/40ce816895b94bfa9a70ea06deb5326f
Autor:
Alexander S. G. Micko, Omar Keritam, Wolfgang Marik, Ben A. Strickland, Robert G. Briggs, Shane Shahrestani, Tyler Cardinal, Engelbert Knosp, Gabriel Zada, Stefan Wolfsberger
Publikováno v:
Journal of Neurosurgery. 137:609-617
OBJECTIVE Dumbbell-shaped pituitary adenomas (DSPAs) are a subgroup of macroadenomas with suprasellar extension that are characterized by a smaller diameter at the level of the diaphragma sellae opening compared with the supradiaphragmal tumor compon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::769798458a14a8069c210554fb273b78
https://doi.org/10.3171/2021.9.jns211689
https://doi.org/10.3171/2021.9.jns211689
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
Autor:
Martin Krenn, Merve Sener, Jakob Rath, Gudrun Zulehner, Omar Keritam, Matias Wagner, Franco Laccone, Stephan Iglseder, Sonja Marte, Manuela Baumgartner, Astrid Eisenkölbl, Christian Liechtenstein, Sabine Rudnik, Stefan Quasthoff, Susanne Grinzinger, Johannes Spenger, Saskia B. Wortmann, Wolfgang N. Löscher, Fritz Zimprich, Anna Kellersmann, Mika Rappold, Günther Bernert, Michael Freilinger, Hakan Cetin
Publikováno v:
Journal of Neurology, 270, 909-916
Journal of Neurology, 270, 2, pp. 909-916
J. Neurol. 270, 909-916 (2023)
Journal of Neurology, 270, 2, pp. 909-916
J. Neurol. 270, 909-916 (2023)
Background Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects resulting in impaired neuromuscular transmission. Although effective treatments are available, CMS is probably underdiagnosed, and syste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eac79402f45ed8b0df3052f7e5df38b
http://hdl.handle.net/2066/291312
http://hdl.handle.net/2066/291312
Autor:
M. Trauner, P Munda, Stefan Traussnigg, Omar Keritam, Peter Ferenci, Judith Stift, Rafael Paternostro, Gerald W. Prager, Emina Halilbasic, Katharina Staufer, AF Stättermayer
Publikováno v:
Zeitschrift für Gastroenterologie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abaa812c1433e160ff58be0fee23ddb6
https://doi.org/10.1055/s-0039-1691910
https://doi.org/10.1055/s-0039-1691910
Autor:
Omar Keritam, Katharina Staufer, Judith Stift, Michael Trauner, Albert Friedrich Stättermayer, Stefan Traussnigg, Rafael Paternostro, Gerhard Prager, P. Munda, Peter ferencl, Emina Halilbasic
Publikováno v:
Journal of Hepatology. 70:e306-e307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaad466a59087e7a47d316ef66ea872c
https://doi.org/10.1016/s0618-8278(19)30596-1
https://doi.org/10.1016/s0618-8278(19)30596-1