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Wiener Medizinische Wochenschrift (1946)|November 11, 2024
Thrombo-CARE-cardioembolic stroke etiology in cryptogenic stroke suggested by fibrin-/platelet-rich clot histology : Thrombo-CARE (configuration analysis to refine etiology)Daniel C Schwarzenhofer, Tim von Oertzen, Serge Weis, et al.Journal of Molecular Neuroscience : MN|August 30, 2007
Meta-analysis of 12 genomic studies in bipolar disorderMichael Elashoff, Brandon W Higgs, Robert H Yolken, et al.Neurobiology of Aging|December 25, 2012
Calcyclin binding protein and Siah-1 interacting protein in Alzheimer's disease pathology: neuronal localization and possible functionUrszula Wasik, Gabriela Schneider, Anna Mietelska-Porowska, et al.Neuro-Oncology|February 13, 2010
O6-Methylguanine DNA methyltransferase protein expression in tumor cells predicts outcome of temozolomide therapy in glioblastoma patientsSabine Spiegl-Kreinecker, Christine Pirker, Martin Filipits, et al.Neuro-Oncology|February 15, 2015
Prognostic quality of activating TERT promoter mutations in glioblastoma: interaction with the rs2853669 polymorphism and patient age at diagnosisSabine Spiegl-Kreinecker, Daniela Lötsch, Bahil Ghanim, et al.British Journal of Cancer|March 24, 2020
Ferritin in glioblastomaHeidi Jaksch-Bogensperger, Sabine Spiegl-Kreinecker, Paolo Arosio, et al.Journal of Neurology|April 5, 2024
Endothelial receptor proteins in acute venous thrombosis and delayed thrombus resolution in cerebral sinus vein thrombosisLukas Kellermair, Christoph Höfer, Matthias W G Zeller, et al.Neuro-Oncology|July 17, 2018
TERT promoter mutations are associated with poor prognosis and cell immortalization in meningiomaSabine Spiegl-Kreinecker, Daniela Lötsch, Katharina Neumayer, et al.Frontiers in Immunology|February 15, 2018
Fatal Necrotizing Encephalopathy after Treatment with Nivolumab for Squamous Non-Small Cell Lung Cancer: Case Report and Review of the LiteratureMarkus Leitinger, Mihael V Varosanec, Slaven Pikija, et al.Genes|December 23, 2023
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic ToolKatarína Kušíková, Andrea Šoltýsová, Andrej Ficek, et al.Pageof 10