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Current Neurology and Neuroscience Reports|December 30, 2011
Syndromes predisposing to pediatric central nervous system tumors: lessons learned and new promisesAnita Villani, David Malkin, Uri TaboriPediatric Blood & Cancer|March 25, 2021
Non-rhabdomyosarcoma soft tissue sarcomas diagnosed in patients at a young age. An overview of clinical, pathological, and molecular findingsSamuele Renzi, Noelle Cullinan, Sarah Cohen-Gogo, et al.Nature Communications|August 27, 2024
Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patternsDerek Wong, Maha Tageldein, Ping Luo, et al.Current Oncology (Toronto, Ont.)|July 28, 2023
Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt LeukemiaSamuele Renzi, Fatimah Algawahmed, Scott Davidson, et al.Pediatric Blood & Cancer|October 13, 2011
Choroid plexus tumors; management, outcome, and association with the Li-Fraumeni syndrome: the Children's Hospital Los Angeles (CHLA) experience, 1991-2010Alexa E Gozali, Barbara Britt, Lisa Shane, et al.American Journal of Human Genetics|November 9, 2010
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromesAdam Shlien, Berivan Baskin, Maria Isabel W Achatz, et al.Current Treatment Options in Pediatrics|April 16, 2024
Precision Child Health: an Emerging Paradigm for Paediatric Quality and SafetyGregory Costain, Ronald D Cohn, David MalkinInternational Journal of Cancer|August 1, 2026
Future Trends in Cancer Prevention and Interception in Cancer Predisposition Syndromes: Leveraging Insights From High-Risk PopulationsYiming Wang, David Malkin, Steven M LipkinCancer Biology & Therapy|December 2, 2011
New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohortRobert K Nam, William Zhang, Katherine Siminovitch, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 6, 2024
tp53 R217H and R242H mutant zebrafish exhibit dysfunctional p53 hallmarks and recapitulate Li-Fraumeni syndrome phenotypesKim Kobar, Lissandra Tuzi, Jennifer A Fiene, et al.Pageof 33