Zobrazeno 1 - 10
of 307
pro vyhledávání: '"Thomas, Czech"'
Autor:
Karl Rössler, Dirk Van Roost, Olaf Schijns, Linda Ackermans, Daniel Delev, Pedro Duarte Batista, Lorand Erőss, Kostas Fountas, Michael Hart, Marie Krüger, Marec von Lehe, Alexandre Rainha Campos, Franziska Schmidt, Ido Strauss, Tom Theys, Thomas Czech, Eyiyemisi Damisah, Christian Dorfer, Martha Feucht, Ellen Gelpi, Enrico Ghizoni, Romana Höftberger, Gregor Kasprian, Klaus Novak, Ekatarina Pataraia, Valerie Quinot, Stefan Rampp, Julia Shawarba, Fabian Winter
Publikováno v:
Brain and Spine, Vol 4, Iss , Pp 103924- (2024)
Externí odkaz:
https://doaj.org/article/b43dd8829a2e416ea541436a04d51973
Autor:
Charlotte Carton, D. Gareth Evans, Ignacio Blanco, Reinhard E. Friedrich, Rosalie E. Ferner, Said Farschtschi, Hector Salvador, Amedeo A. Azizi, Victor Mautner, Claas Röhl, Sirkku Peltonen, Stavros Stivaros, Eric Legius, Rianne Oostenbrink, Joan Brunet, Frank Van Calenbergh, Catherine Cassiman, Thomas Czech, María José Gavarrete de León, Henk Giele, Susie Henley, Conxi Lazaro, Vera Lipkovskaya, Eamonn R. Maher, Vanessa Martin, Irene Mathijssen, Enrico Opocher, Ana Elisabete Pires, Thomas Pletschko, Eirene Poupaki, Vita Ridola, Andre Rietman, Thorsten Rosenbaum, Alastair Santhouse, Astrid Sehested, Ian Simmons, Walter Taal, Anja Wagner
Publikováno v:
EClinicalMedicine, Vol 56, Iss , Pp 101818- (2023)
Summary: Background: Neurofibromatosis type 1 (NF1) is a multisystem genetic disorder, predisposing development of benign and malignant tumours. Given the oncogenic potential, long-term surveillance is important in patients with NF1. Proposals for NF
Externí odkaz:
https://doaj.org/article/413a0a790cef49bea14006073668941d
Autor:
Katarina Bartalska, Verena Hübschmann, Medina Korkut-Demirbaş, Ryan John A. Cubero, Alessandro Venturino, Karl Rössler, Thomas Czech, Sandra Siegert
Publikováno v:
iScience, Vol 25, Iss 7, Pp 104580- (2022)
Summary: Cerebral organoids differentiated from human-induced pluripotent stem cells (hiPSC) provide a unique opportunity to investigate brain development. However, organoids usually lack microglia, brain-resident immune cells, which are present in t
Externí odkaz:
https://doaj.org/article/37bd4fbfc5574e879866be0add17f1a6
Autor:
Natalia Stepien, Christine Haberler, Sarah Theurer, Maria-Theresa Schmook, Carola Lütgendorf-Caucig, Leonhard Müllauer, Johannes Gojo, Amedeo A. Azizi, Thomas Czech, Irene Slavc, Andreas Peyrl
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Neuroendocrine tumors (NETs) are rare neoplasms predominantly arising in the gastrointestinal-tract or the lungs of adults. To date, only ten cases of primary central nervous system (CNS) NETs have been reported, with just three of them describing a
Externí odkaz:
https://doaj.org/article/687fe07356514865bdee0dc6cfc84df4
Autor:
Beatrix Wulkersdorfer, Martin Bauer, Rudolf Karch, Harald Stefanits, Cécile Philippe, Maria Weber, Thomas Czech, Marie-Claude Menet, Xavier Declèves, Johannes A. Hainfellner, Matthias Preusser, Marcus Hacker, Markus Zeitlinger, Markus Müller, Oliver Langer
Publikováno v:
EJNMMI Research, Vol 9, Iss 1, Pp 1-10 (2019)
Abstract Background P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) are two efflux transporters expressed at the blood–brain barrier which effectively restrict the brain distribution of the majority of currently known anticancer
Externí odkaz:
https://doaj.org/article/beb34f2037d5499f8f88efbca9a30902
Autor:
Lisa Gabler, Daniela Lötsch, Dominik Kirchhofer, Sushilla van Schoonhoven, Hannah M. Schmidt, Lisa Mayr, Christine Pirker, Katharina Neumayer, Carina Dinhof, Lucia Kastler, Amedeo A. Azizi, Christian Dorfer, Thomas Czech, Christine Haberler, Andreas Peyrl, Rajiv Kumar, Irene Slavc, Sabine Spiegl-Kreinecker, Johannes Gojo, Walter Berger
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
Abstract The BRAF gene and the TERT promoter are among the most frequently altered genomic loci in low-grade (LGG) and high-grade-glioma (HGG), respectively. The coexistence of BRAF and TERT promoter aberrations characterizes a subset of aggressive g
Externí odkaz:
https://doaj.org/article/0d0f5c425b5246679d273f73084e3798
Autor:
Sibylle Madlener, Julia Furtner, Natalia Stepien, Daniel Senfter, Lisa Mayr, Maximilian Zeyda, Leon Gramss, Barbara Aistleitner, Sabine Spiegl-Kreinecker, Elisa Rivelles, Christian Dorfer, Karl Rössler, Thomas Czech, Amedeo A. Azizi, Andreas Peyrl, Daniela Lötsch-Gojo, Leonhard Müllauer, Christine Haberler, Irene Slavc, Johannes Gojo
Publikováno v:
Acta Neuropathologica. 145:843-846
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::946e618d7bc855da64a930bb3267377f
https://doi.org/10.1007/s00401-023-02567-z
https://doi.org/10.1007/s00401-023-02567-z
Autor:
Philip Pruckner, Karl‐Heinz Nenning, Florian Ph.S Fischmeister, Mehmet‐Salih Yildirim, Michelle Schwarz, Andreas Reitner, Susanne Aull‐Watschinger, Johannes Koren, Christoph Baumgartner, Daniela Prayer, Karl Rössler, Christian Dorfer, Thomas Czech, Ekaterina Pataraia, Gregor Kasprian, Silvia Bonelli
Publikováno v:
Epilepsia. 64:705-717
Anterior temporal lobectomy (ATL) and transsylvian selective amygdalohippocampectomy (tsSAHE) are effective treatment strategies for intractable temporal lobe epilepsy but may cause visual field deficits (VFDs) by damaging the optic radiation (OpR).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb38b07644837c2ff5844a038038cc0
https://doi.org/10.1111/epi.17490
https://doi.org/10.1111/epi.17490
Autor:
Lisa Mayr, Johannes Gojo, Andreas Peyrl, Amedeo A. Azizi, Natalia M. Stepien, Thomas Pletschko, Thomas Czech, Christian Dorfer, Sander Lambo, Karin Dieckmann, Christine Haberler, Marcel Kool, Irene Slavc
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Embryonal tumor with multilayered rosettes (ETMR) is a rare, aggressive embryonal central nervous system tumor characterized by LIN28A expression and alterations in the C19MC locus. ETMRs predominantly occur in young children, have a dismal prognosis
Externí odkaz:
https://doaj.org/article/bc74f8f9dbc94b85bc346c956b44e4fc
Autor:
Johannes Gojo, Zdenek Pavelka, Danica Zapletalova, Maria T. Schmook, Lisa Mayr, Sibylle Madlener, Michal Kyr, Klara Vejmelkova, Martin Smrcka, Thomas Czech, Christian Dorfer, Jarmila Skotakova, Amedeo A. Azizi, Monika Chocholous, Dominik Reisinger, David Lastovicka, Dalibor Valik, Christine Haberler, Andreas Peyrl, Hana Noskova, Karol Pál, Marta Jezova, Renata Veselska, Sarka Kozakova, Ondrej Slaby, Irene Slavc, Jaroslav Sterba
Publikováno v:
Frontiers in Oncology, Vol 9 (2020)
Diffuse gliomas with K27M histone mutations (H3K27M glioma) are generally characterized by a fatal prognosis, particularly affecting the pediatric population. Based on the molecular heterogeneity observed in this tumor type, personalized treatment is
Externí odkaz:
https://doaj.org/article/aae136c1580e43fabf033e1522e3cb53