检索结果 - Ströbel, Thomas
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FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A repor... 由 Rusina, Robert, Kovacs, Gabor G, Fiala, Jindřich, Hort, Jakub, Ridzoň, Petr, Holmerová, Iva, Ströbel, Thomas, Matěj, Radoslav
出版 2011Text -
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Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C “Strain” 由 Gelpi, Ellen, Klotz, Sigrid, Vidal-Robau, Nuria, Ricken, Gerda, Regelsberger, Günther, Ströbel, Thomas, Kalev, Ognian, Leoni, Marlene, Budka, Herbert, Kovacs, Gabor G.
出版 2021Text -
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Genetically Engineered Microvesicles Carrying Suicide mRNA/Protein Inhibit Schwannoma Tumor Growth 由 Mizrak, Arda, Bolukbasi, Mehmet Fatih, Ozdener, Gokhan Baris, Brenner, Gary J, Madlener, Sibylle, Erkan, Erdogan Pekcan, Ströbel, Thomas, Breakefield, Xandra O, Saydam, Okay
出版 2013Text -
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Ape1 guides DNA repair pathway choice that is associated with drug tolerance in glioblastoma 由 Ströbel, Thomas, Madlener, Sibylle, Tuna, Serkan, Vose, Sarah, Lagerweij, Tonny, Wurdinger, Thomas, Vierlinger, Klemens, Wöhrer, Adelheid, Price, Brendan D., Demple, Bruce, Saydam, Okay, Saydam, Nurten
出版 2017Text -
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KINFix – A formalin-free non-commercial fixative optimized for histological, immunohistochemical and molecular analyses of neurosurgical tissue specimens 由 Stefanits, Harald, Bieńkowski, Michał, Galanski, Markus, Mitulović, Goran, Ströbel, Thomas, Gelpi, Ellen, Ribalta, Teresa, Broholm, Helle, Hartmann, Christian, Kros, Johan M., Preusser, Matthias, Hainfellner, Johannes A.
出版 2016Text -
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Dura mater is a potential source of Aβ seeds 由 Kovacs, Gabor G., Lutz, Mirjam I., Ricken, Gerda, Ströbel, Thomas, Höftberger, Romana, Preusser, Matthias, Regelsberger, Günther, Hönigschnabl, Selma, Reiner, Angelika, Fischer, Peter, Budka, Herbert, Hainfellner, Johannes A.
出版 2016Text -
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Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease 由 Klotz, Sigrid, König, Theresa, Erdler, Marcus, Ulram, Andreas, Nguyen, Anita, Ströbel, Thomas, Zimprich, Alexander, Stögmann, Elisabeth, Regelsberger, Günther, Höftberger, Romana, Budka, Herbert, Kovacs, Gabor G., Gelpi, Ellen
出版 2020Text -
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SNP-array based whole genome homozygosity mapping: A quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients() 由 Papić, Lea, Fischer, Dirk, Trajanoski, Slave, Höftberger, Romana, Fischer, Carina, Ströbel, Thomas, Schmidt, Wolfgang M., Bittner, Reginald E., Schabhüttl, Maria, Gruber, Karin, Pieber, Thomas R., Janecke, Andreas R., Auer-Grumbach, Michaela
出版 2011Text -
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Inter‐Laboratory Assessment of PrP(Sc) Typing in Creutzfeldt–Jakob Disease: A Western Blot Study within the NeuroPrion Consortium 由 Parchi, Piero, Notari, Silvio, Weber, Petra, Schimmel, Heinz, Budka, Herbert, Ferrer, Isidre, Haik, Stéphane, Hauw, Jean‐Jacques, Head, Mark W, Ironside, James W, Limido, Lucia, Rodriguez, Agustin, Ströbel, Thomas, Tagliavini, Fabrizio, Kretzschmar, Hans A.
出版 2008Text -
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Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study 由 Ferrer, Isidre, Armstrong, Judith, Capellari, Sabina, Parchi, Piero, Arzberger, Thomas, Bell, Jeanne, Budka, Herbert, Ströbel, Thomas, Giaccone, Giorgio, Rossi, Giacomina, Bogdanovic, Nenad, Fakai, Peter, Schmitt, Andrea, Riederers, Peter, Al‐Sarraj, Safa, Ravid, Rivka, Kretzschmar, Hans
出版 2007Text -
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Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity? 由 Kovacs, Gabor G, Peden, Alexander, Weis, Serge, Höftberger, Romana, Berghoff, Anna S, Yull, Helen, Ströbel, Thomas, Koppi, Stefan, Katzenschlager, Regina, Langenscheidt, Dieter, Assar, Hamid, Zaruba, Elisabeth, Gröner, Albrecht, Voigtländer, Till, Puska, Gina, Hametner, Eva, Grams, Astrid, Muigg, Armin, Knoflach, Michael, László, Lajos, Ironside, James W, Head, Mark W, Budka, Herbert
出版 2013Text