Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Brittany M Szymaniak"'
Autor:
Jonathan A. Aguiar, Eric V. Li, Mohammad R. Siddiqui, Moataz A. Soliman, Sai K. S. R. Kumar, Edward M. Schaeffer, Mary Kate Keeter, C. Hendricks Brown, Brittany M. Szymaniak, Ashley E. Ross
Publikováno v:
The Prostate. 83:516-523
Genetic evaluation of men with advanced prostate cancer is recognized as imperative both to guide treatment decisions and to trigger cascade genetic testing of family members. Here we investigate utilization patterns of genetic testing among a contem
Publikováno v:
Current Opinion in Supportive & Palliative Care. 15:241-246
PURPOSE OF REVIEW Recent advances in our understanding of prostate cancer genetics have transformed the field. However, challenges in implementation and clinical application remain. The aim of this review is to discuss recent noteworthy publications
Publikováno v:
Urologic Clinics of North America. 48:365-371
Germline testing should be performed to support treatment selection for patients with metastatic prostate cancer, and should be identified in patients with high-risk localized disease. Patients with germline BRCA1/2 mutations should be educated regar
Autor:
Yue Zhang, Catherine C Nguyen, Nigel T Zhang, Nicolas S Fink, Jordan D John, Omkar G Venkatesh, Jonathan D Roe, Steven C Hoffman, Maciej S Lesniak, Jean-Paul Wolinsky, Craig Horbinski, Brittany M Szymaniak, Robin A Buerki, Jeffrey A Sosman, Niraj K Shenoy, Rimas V Lukas
Publikováno v:
Neuro-oncology.
Von Hippel-Lindau (VHL) disease is a tumor predisposition syndrome caused by mutations in the VHL gene that presents with visceral neoplasms and growths, including clear cell renal cell carcinoma, and central nervous system manifestations, such as he
Autor:
Daniel C. Danila, Daniel J. George, Celestia S. Higano, Charles J. Ryan, Veda N. Giri, Ana M. Molina, Zachery R. Reichert, Rana R. McKay, Julie N. Graff, Elisabeth I. Heath, Young E. Whang, Alicia K. Morgans, Emmanuel S. Antonarakis, Mary-Ellen Taplin, Akash Patnaik, Jake Vinson, Channing J. Paller, Matthew Rettig, Heather H. Cheng, Mallika Sachdev Dhawan, Tomasz M. Beer, Brittany M. Szymaniak, Maria I. Carlo, Glenn Liu, Lauren A. Facchini, Daniel P. Petrylak, Shilpa Gupta
Publikováno v:
JCO oncology practice, vol 16, iss 12
JCO Oncol Pract
JCO Oncol Pract
Germline genetic testing is now routinely recommended for patients with prostate cancer (PCa) because of expanded guidelines and options for targeted treatments. However, integrating genetic testing into oncology and urology clinical workflows remain
Autor:
Brittany M. Szymaniak, Lauren A. Facchini, Max F. Kelsten, Heather H. Cheng, Alicia K. Morgans
Publikováno v:
Urologic Oncology ISBN: 9783030898908
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b64240dda654207290b569d5b910b7a
https://doi.org/10.1007/978-3-030-89891-5_3
https://doi.org/10.1007/978-3-030-89891-5_3
Autor:
Jennifer M, Weiss, Samir, Gupta, Carol A, Burke, Lisen, Axell, Lee-May, Chen, Daniel C, Chung, Katherine M, Clayback, Susan, Dallas, Seth, Felder, Olumide, Gbolahan, Francis M, Giardiello, William, Grady, Michael J, Hall, Heather, Hampel, Rachel, Hodan, Gregory, Idos, Priyanka, Kanth, Bryson, Katona, Laura, Lamps, Xavier, Llor, Patrick M, Lynch, Arnold J, Markowitz, Sara, Pirzadeh-Miller, Niloy Jewel, Samadder, David, Shibata, Benjamin J, Swanson, Brittany M, Szymaniak, Georgia L, Wiesner, Andrew, Wolf, Matthew B, Yurgelun, Mae, Zakhour, Susan D, Darlow, Mary A, Dwyer, Mallory, Campbell
Publikováno v:
Journal of the National Comprehensive Cancer Network : JNCCN. 19(10)
Identifying individuals with hereditary syndromes allows for timely cancer surveillance, opportunities for risk reduction, and syndrome-specific management. Establishing criteria for hereditary cancer risk assessment allows for the identification of
Publikováno v:
Retinal casesbrief reports.
Purpose To present the case of a family with a novel PRPH2/RDS mutation. Methods A case report. Patients A 44 year old female and her immediate family, including a father and sister who shared her PRPH2/RDS mutation. Results A 44 year old female pres
Autor:
Robert Pilarski, Arthur L. Burnett, Lucia R. Languino, Colette Hyatt, Jacqueline Powers, Robert B. Den, Alberto Briganti, Veda N. Giri, Lorelei A. Mucci, Daniel P. Petrylak, Oliver Sartor, Amie Blanco, Daniel W. Lin, Himisha Beltran, E. David Crawford, Karen E. Knudsen, Mary-Ellen Taplin, Brian T. Helfand, Felix Y. Feng, Costas D. Lallas, E. Michael D. Scott, Wayne H. Pinover, R. Jeffrey Karnes, Scott Weissman, Evan Y. Yu, Timothy R. Rebbeck, Ashley H. Woodson, Matthew J. Schiewer, Todd M. Morgan, William B. Isaacs, Jeffrey N. Weitzel, Alanna Kulchak Rahm, Michael S. Cookson, James A. Eastham, S. Bruce Malkowicz, Neha Vapiwala, Kevin R. Loughlin, Raoul S. Concepcion, Ana Maria Lopez, Jose Moreno, Brock O'Neil, Patrick T. Gomella, Patrick Mille, Charnita Zeigler-Johnson, Howard M. Sandler, Kathleen A. Cooney, William Tester, Sarah M. Nielsen, Thomas J. Polascik, Richard C. Wender, Howard R. Soule, Ronald E. Myers, Scott E. Eggener, Marc B. Garnick, Stacy Loeb, Martin Miner, Anthony J. Costello, Gerald L. Andriole, Amanda E. Toland, David Y.T. Chen, Albert Dobi, Joseph K Izes, Mary B. Daly, Leonard G. Gomella, Mark D. Hurwitz, J. Kellogg Parsons, Matthew L. Freedman, Nathan Handley, Adam P. Dicker, Jianfeng Xu, Michael Russell Mullane, Charles J. Ryan, Edouard J. Trabulsi, Anne Calvaresi, James Ryan Mark, Thenappan Chandrasekar, Colin C. Pritchard, Saud H. AlDubayan, Curtis A. Pettaway, William Kevin Kelly, Lindsey Byrne, Peter R. Carroll, Brittany M. Szymaniak, Alicia K. Morgans, Peter A. Pinto, William L. Dahut, Mark Mann, Ganesh V. Raj, James L. Mohler, Wendy Poage, Heather H. Cheng, Grace L. Lu-Yao
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, vol 38, iss 24
PURPOSE Germline testing (GT) is a central feature of prostate cancer (PCA) treatment, management, and hereditary cancer assessment. Critical needs include optimized multigene testing strategies that incorporate evolving genetic data, consistency in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a0090e4e87cd120ef0899e6263c77c
https://escholarship.org/uc/item/3mg229rb
https://escholarship.org/uc/item/3mg229rb
Publikováno v:
The Canadian journal of urology. 26(5 Suppl 2)
The landscape of genetic testing for prostate cancer is rapidly evolving. There is increasing evidence that individuals with germline mutations in DNA-repair genes are more responsive to targeted therapies. Due to potential implications for treatment