Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Emily Jonczak"'
Autor:
Junaid Arshad, Priscila Barreto-Coelho, Emily Jonczak, Andrea Espejo, Gina D’Amato, Jonathan C. Trent
Publikováno v:
Journal of Immunotherapy and Precision Oncology, Pp 64-68 (2020)
Background: Leiomyosarcoma is a malignant mesenchymal tumor of cells of smooth muscle lineage arising commonly in retroperitoneum, uterus, large veins, and the limbs. The genetics of leiomyosarcomas are complex and there is very limited understanding
Externí odkaz:
https://doaj.org/article/fc35834872b14921b641ccaa4d7701af
Autor:
Jamie E. Clarke, Stephanie Magoon, Irman Forghani, Francesco Alessandrino, Gina D’Amato, Emily Jonczak, Ty K. Subhawong
Publikováno v:
European Journal of Radiology Open, Vol 9, Iss , Pp 100422- (2022)
Hereditary cancer syndromes comprise an important subset of cancers caused by pathogenic germline mutations that can affect various organ systems. Radiologic screening and surveillance for solid tumors has emerged as a critical component of patient m
Externí odkaz:
https://doaj.org/article/d7ac620c78d24b0b95a4993f0b241778
Autor:
Steven Bialick, Leticia Campoverde, Jesus Antonio Ocejo Gallegos, Priscila Barreto-Coelho, Aleksandra Watson, Kshitij Arora, Andres Perez, Esdras Lopez, Shree Venkat, Andrew E. Rosenberg, Brooke Crawford, Emily Jonczak, Jonathan Trent, Aditi Dhir, Gina D’Amato
Publikováno v:
Current Treatment Options in Oncology. 24:528-541
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb550889242d5ac4b97647b621110e21
https://doi.org/10.1007/s11864-023-01073-4
https://doi.org/10.1007/s11864-023-01073-4
Autor:
Seiya Liu, Carey Green, David S. Lee, Elizabeth Montgomery, Ty K. Subhawong, Andrew E. Rosenberg, Jonathan C. Trent, Emily Jonczak, Gina D'Amato
Inflammatory myofibroblastic tumors (IMT) are spindle cell neoplasms with myofibroblastic differentiation and inflammatory infiltration that are typically benign in presentation but can present aggressively in rare circumstances. We herein report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::99864e0683924607300f6ff8a2e7f671
https://zenodo.org/record/7936397
https://zenodo.org/record/7936397
Heterogenous Intertumoral KIT Mutations in Long-term Stage 4 Gastrointestinal Stromal Tumor Survivor
Autor:
Seiya Liu, Irene Goo, Ty K. Subhawong, Andrew E. Rosenberg, Jonathan C Trent, Emily Jonczak, Elizabeth Montgomery, Alan Livingstone, Gina D'Amato
Gastrointestinal stromal tumors (GISTs) are mesenchymal neoplasms of the gastrointestinal tract, with a prevalence of 5% out of all sarcomas. We herein report the case of a 54-year-old man with metastatic GIST who initially presented to the emergency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::46f0bce24dc6add9c7a8aca7bde53b12
https://zenodo.org/record/7935852
https://zenodo.org/record/7935852
Autor:
Andrea P. Espejo, Jonathan C. Trent, Priscila Barreto-Coelho, Emily Jonczak, Junaid Arshad, Gina Z. D'Amato
Publikováno v:
J Immunother Precis Oncol
Background Leiomyosarcoma is a malignant mesenchymal tumor of cells of smooth muscle lineage arising commonly in retroperitoneum, uterus, large veins, and the limbs. The genetics of leiomyosarcomas are complex and there is very limited understanding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0feee562d7738ade41809b062ede0d95
https://doi.org/10.36401/jipo-20-3
https://doi.org/10.36401/jipo-20-3
Autor:
Jonathan C. Trent, Andrew E. Rosenberg, Andrea P. Espejo-Freire, Andrew Elliott, Don S. Dizon, Margaret von Mehren, Ty K. Subhawong, Julio A. Diaz-Perez, Daniel Magee, Emily Jonczak, Junaid Arshad, William M. Korn, A. Hussein, Matthew J. Oberley, Priscila Barreto-Coelho, Philippos Apolinario Costa, Gina Z. D'Amato, Kirsten M. Leu, Moh’d M. Khushman
Publikováno v:
Cancers
Cancers; Volume 13; Issue 19; Pages: 4816
Cancers, Vol 13, Iss 4816, p 4816 (2021)
Cancers; Volume 13; Issue 19; Pages: 4816
Cancers, Vol 13, Iss 4816, p 4816 (2021)
Simple Summary Angiosarcomas (AS) are rare, highly aggressive sarcomas with limited therapeutic options. Genomic sequencing techniques have identified recurrent genetic abnormalities. Nevertheless, the association of these findings with etiology, sit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6904ed4c316d758273b339011db504b
http://europepmc.org/articles/PMC8507700
http://europepmc.org/articles/PMC8507700
Autor:
Philippos Apolinario Costa, Arshia Arora, Heng Tan, Yanelys Fernandez, Leticia Campoverde, Priscila Barreto Coelho, Steven Bialick, Andrea P. Espejo-Freire, Emily Jonczak, Gina Z. D'Amato, Ty Subhawong, Jonathan C. Trent
Publikováno v:
Journal of Clinical Oncology. 40:e23534-e23534
e23534 Background: Many systemic treatment options are described for desmoid tumors, including hormonal therapies, non-steroidal anti-inflammatory drugs, cytotoxic chemotherapeutic agents, and most recently, tyrosine kinase inhibitors. Although many
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::043c4c6edc60cc1f9a107461c3fc38fb
https://doi.org/10.1200/jco.2022.40.16_suppl.e23534
https://doi.org/10.1200/jco.2022.40.16_suppl.e23534
Autor:
Andrea P. Espejo-Freire, Leticia Campoverde, Yana Kropotova, Kurt Statz-Geary, Philippos Apolinario Costa, Priscila Barreto Coelho, Steven Bialick, Gina Z. D'Amato, Emily Jonczak, Jonathan C. Trent, Aditi Dhir
Publikováno v:
Journal of Clinical Oncology. 40:e23508-e23508
e23508 Background: Bone sarcomas account for about 5% of cancers in adolescents and young adults (AYA). Outcomes in this population are consistently inferior than children. It is poorly understood whether this is related to the tumor biology or the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e7f6df3bda310828ab5d185241a2596
https://doi.org/10.1200/jco.2022.40.16_suppl.e23508
https://doi.org/10.1200/jco.2022.40.16_suppl.e23508
Publikováno v:
Operative Techniques in Orthopaedics. 32:100960
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58149cc5d55ef89c18676c093fda7e7e
https://doi.org/10.1016/j.oto.2022.100960
https://doi.org/10.1016/j.oto.2022.100960