Neoplastic Syndromes, Hereditary

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Ercan, A. B., Aronson, M., Fernandez, N. R., Chang, Y., Levine, A., Liu, Z. A., Negm, L., Edwards, M., Bianchi, V., Stengs, L., Chung, J., Al-Battashi, A., Reschke, A., Lion, A., Ahmad, A., Lassaletta, A., Reddy, A. T., Al-Darraji, A. F., Shah, A. C., … Tabori, U. (2024). Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study. The Lancet Oncology, 25(5), 668–682. https://doi.org/10.1016/s1470-2045(24)00026-3
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Elez, E., Kopetz, S., Tabernero, J., Bekaii-Saab, T., Taieb, J., Yoshino, T., Manji, G., Fernandez, K., Abbattista, A., Zhang, X., & Morris, V. K. (2024). SEAMARK: phase II study of first-line encorafenib and cetuximab plus pembrolizumab for MSI-H/dMMR BRAF V600E-mutant mCRC. Future Oncology, 20(11), 653–663. https://doi.org/10.2217/fon-2022-1249
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Joseph, G., Lindberg, N. M., Guerra, C., Hernandez, C., Karliner, L. S., Gilmore, M. J., Zepp, J., Rolf, B. A., Caruncho, M., Riddle, L., Kauffman, T. L., Leo, M. C., & Wilfond, B. S. (2023). Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome. Journal of Genetic Counseling, 32(4), 870–886. Portico. https://doi.org/10.1002/jgc4.1695
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Zeng, C., Bastarache, L. A., Tao, R., Venner, E., Hebbring, S., Andujar, J. D., Bland, H. T., Crosslin, D. R., Pratap, S., Cooley, A., Pacheco, J. A., Christensen, K. D., Perez, E., Zawatsky, C. L. B., Witkowski, L., Zouk, H., Weng, C., Leppig, K. A., Sleiman, P. M. A., … Denny, J. C. (2022). Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases. JAMA Oncology, 8(6), 835. https://doi.org/10.1001/jamaoncol.2022.0373
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