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Virchows Archiv : an International Journal of Pathology|February 2, 2021
Mantle cell lymphomas with concomitant MYC and CCND1 breakpoints are recurrently TdT positive and frequently show high-grade pathological and genetic featuresSietse M Aukema, Giorgio A Croci, Susanne Bens, et al.Hemasphere|May 1, 2026
Chronic lymphocytic leukemia with <i>IGH</i>::<i>BCL3</i>-translocation is characterized by a homogeneous and distinct genetic and epigenetic landscapeCosima Drewes, Cristina López, Juan Emilio Martinez-Manjón, et al.The American Journal of Surgical Pathology|April 21, 2022
SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni SyndromeMartin Hasselblatt, Christian Thomas, Aniello Federico, et al.Leukemia|April 23, 2026
The spectrum of immunoglobulin heavy chain enhancer hijacking in chronic lymphocytic leukemiaCosima Drewes, Cristina López, Nnamdi Okeke, et al.Brain Pathology (Zurich, Switzerland)|July 7, 2016
Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcomePascal D Johann, Volker Hovestadt, Christian Thomas, et al.Genes, Chromosomes & Cancer|November 3, 2019
Reconstruction of rearranged T-cell receptor loci by whole genome and transcriptome sequencing gives insights into the initial steps of T-cell prolymphocytic leukemiaPaurnima Patil, Agata Cieslak, Stephan H Bernhart, et al.Human Reproduction (Oxford, England)|August 8, 2023
Rhabdoid tumors in patients conceived following ART: is there an association?Karolina Nemes, Martin Benesch, Julia Kolarova, et al.Acta Neuropathologica|November 17, 2019
Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adultsChristian Thomas, Annika Wefers, Susanne Bens, et al.Cancer Research|August 1, 2022
Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial CancerOwen J Chen, Ester Castellsagué, Mohamed Moustafa-Kamal, et al.Acta Neuropathologica|May 2, 2022
ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significanceAniello Federico, Christian Thomas, Katarzyna Miskiewicz, et al.Pageof 9