Cargando…
RARE-19. PEDIATRIC HIGH GRADE GLIOMA WITH DNA REPAIR PATHWAY ABERRATIONS, CLINICAL CHARACTERISTICS AND OUTCOME
DNA mismatch repair machinery is an integral part of the human genome and its defect has been involved in tumorigenesis and treatment resistance. Heterozygous monoallelic germline loss of function in MLH-1, MSH-2, MSH-6 or PMS-2 is involved in Lynch syndrome, whereas biallelic mutations cause consti...
Autores principales: | Baig, Muhammad, McCall, David, Moss, Tyler, Sandberg, David, Fuller, Gregory, McGovern, Susan, Paulino, Arnold, Najjar, Amer, Chandra, Joya, Khatua, Soumen, Zaky, Wafik |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715083/ http://dx.doi.org/10.1093/neuonc/noaa222.730 |
Ejemplares similares
-
RARE-44. CLINICAL CHARACTERIZATION AND OUTCOME; OUR EXPERIENCE OF CHORDOMAS IN PEDIATRIC AND YOUNG ADULTS
por: Gibson, Amber, et al.
Publicado: (2020) -
RARE-08. Profiling of recurrent adamantinomatous cranionpharyngioma confirms the activation of the MAPK pathway and identifies copy number aberrations in relapsed tumours
por: Apps, John, et al.
Publicado: (2022) -
RARE-23. DIFFUSE LEPTOMENINGEAL GLIONEURONAL TUMOR: A CASE SERIES
por: Aaroe, Ashley, et al.
Publicado: (2021) -
RARE-27. Treatment and outcomes in atypical choroid plexus papilloma: a single institution experience
por: Cluster, Andrew, et al.
Publicado: (2022) -
RARE-32. Phase 0 and feasibility single-institution clinical trial of intravenous tocilizumab for adamantinomatous craniopharyngioma
por: Dorris, Kathleen, et al.
Publicado: (2022)