Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Amanda Anson"'
Autor:
Luke O. Buchmann, Bonita Bennett, Debbie L. Cohen, Michelle F. Jacobs, Lauren Fishbein, Anne Naumer, Maria Bonanni, Heather Wachtel, Katherine L. Nathanson, Amanda Schaefer, Samantha Greenberg, Amanda Anson, Tobias Else, Wendy Kohlmann
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Purpose: Minimal data exist regarding the efficacy of screening protocols for individuals with SDHx germline pathogenic variants with Hereditary Paraganglioma-Pheochromocytoma Syndrome. This study aimed to evaluate the SDHx-related tumor detection ra
Impact of COVID-19 on individuals with paraganglioma/pheochromocytoma history and/or hereditary risk
Autor:
Samantha Greenberg, Nicholas Yozamp, Amanda Anson, Sarah Brand, Luke Buchmann, Wendy Kohlmann, Sara Low, Bob Wong, Tobias Else, Anand Vaidya, Lauren Fishbein
Publikováno v:
Journal of Clinical Oncology. 40:10613-10613
10613 Background: Patients with paraganglioma/pheochromocytoma (PPGL) or hereditary predisposition to PPGL often need screening with biochemical labs, imaging and physical exam. Given the rarity of PPGL and hereditary PPGL, care is often provided thr
Comparing pretest video genetic education for prostate cancer patients: Do patients need assistance?
Autor:
Samantha Greenberg, Elizabeth Orlando, Morgan Devlin, Sara Low, Amanda Anson, Brock O Neil, Wendy Kohlmann, Bob Wong, Christopher B. Dechet, Alejandro Sanchez, Jonathan David Tward, Skyler B Johnson, Neeraj Agarwal, Manish Kohli, Sumati Gupta, Umang Swami, Benjamin L. Maughan
Publikováno v:
Journal of Clinical Oncology. 40:5061-5061
5061 Background: Expanded germline genetic testing recommendations for individuals with prostate cancer (PCa) have resulted in increased demand for pre-test genetic education. As a result, alternative service delivery models in genetic counseling (GC
Autor:
Lauren Fishbein, Amanda Schaefer, Debbie L. Cohen, Samantha Greenberg, Amanda Anson, Tobias Else, Katherine L. Nathanson, Heather Wachtel, Michelle F. Jacobs, Wendy Kohlmann, Maria Bonnani, Anne Naumer, Luke O. Buchmann, Bonita Bennett
Publikováno v:
Journal of Clinical Oncology. 38:1545-1545
1545 Background: Patients with germline pathogenic variants (PVs) in the SDHx genes have increased risk for paragangliomas/pheochromocytomas (PGL/PCC), renal cell carcinomas, and gastrointestinal stromal tumors. Expert recommendation suggests individ