Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Bhuvana A. Setty"'
Autor:
Rituraj Upadhyay, Brett Klamer, Jennifer Matsui, Vikram B. Chakravarthy, Thomas Scharschmidt, Nicholas Yeager, Bhuvana A. Setty, Timothy P. Cripe, Ryan D. Roberts, Jennifer H. Aldrink, Raj Singh, Raju R. Raval, Joshua D. Palmer, Sujith Baliga
Publikováno v:
Cancers, Vol 16, Iss 11, p 2090 (2024)
Background: Pediatric patients with metastatic and/or recurrent solid tumors have poor survival outcomes despite standard-of-care systemic therapy. Stereotactic ablative radiation therapy (SABR) may improve tumor control. We report the outcomes with
Externí odkaz:
https://doaj.org/article/c5c789d8e4434b19825466c798b94920
Autor:
Jordan N. Halsey, Esteban Fernandez Faith, Suzanna J. Logan, Archana Shenoy, Kathleen M. Schieffer, Catherine E. Cottrell, Anna P. Lillis, Jennifer H. Aldrink, Bhuvana A. Setty, Gregory D. Pearson
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2022 (2022)
Syringocystadenocarcinoma papilliferum (SCACP) is a rare malignant neoplasm arising from adnexal tissues and is the malignant complement to the benign neoplasm syringocystadenoma papilliferum (SCAP). SCACP lesions appear as raised nodules or inflamma
Externí odkaz:
https://doaj.org/article/2b4795dd71d2490d9df0736f28522d5b
Autor:
Joel C. Thompson, Gary M. Woods, Michael A. Arnold, Charles Elmaraghy, Samir B. Kahwash, Timothy P. Cripe, Bhuvana A. Setty
Publikováno v:
Case Reports in Oncology, Vol 9, Iss 2, Pp 447-453 (2016)
Pediatric soft tissue sarcomas of the oral/maxillofacial region are rare neoplasms that present significant difficulty with respect to treatment and local control measures. We report four cases of pediatric oral/maxillofacial soft tissue sarcomas fro
Externí odkaz:
https://doaj.org/article/e9b7bb99ea8a4101b3291eef18a7d92a
Autor:
Bhuvana A. Setty, Yi Jin, Peter J. Houghton, Nicholas D. Yeager, Thomas G. Gross, Leif D. Nelin
Publikováno v:
Cellular Physiology and Biochemistry, Vol 39, Iss 2, Pp 802-813 (2016)
Background/Aims: Despite significant advancements in the diagnosis and treatment of osteosarcoma, the overall survival has remained relatively unchanged for over two decades. Hypoxic conditions have been demonstrated in solid tumors and are associate
Externí odkaz:
https://doaj.org/article/de05e5d70d394082b92f9ff11ca90a11
Autor:
Selene C. Koo, Kathleen M. Schieffer, Kristy Lee, Ajay Gupta, Ruthann B. Pfau, Matthew R. Avenarius, Eileen Stonerock, Stephanie LaHaye, James Fitch, Bhuvana A. Setty, Ryan Roberts, Mark Ranalli, Miriam R. Conces, Fang Bu, Elaine R. Mardis, Catherine E. Cottrell
Publikováno v:
Genes, Chromosomes and Cancer. 62:17-26
Next-generation sequencing (NGS) assays can sensitively detect somatic variation, and increasingly can enable the identification of complex structural rearrangements. A subset of infantile spindle cell sarcomas, particularly congenital mesoblastic ne
Publikováno v:
Pediatric Drugs.
Autor:
Marcelo de Souza Fernandez Pereira, David R. Carr, Margaret E. Gatti-Mays, Mallery R. Olsen, Bhuvana A. Setty, Kathryn T. Shahwan, Dean A. Lee
Publikováno v:
Cancer journal (Sudbury, Mass.). 28(4)
Natural killer (NK) cells possess an innate ability to recognize cancer and are key mediators of cytotoxic efficacy for anticancer antibodies. Recent advances in the ability to generate, qualify, and safely infuse NK cells have led to a wide variety
Autor:
Ying-Chen Claire Hou, Michael J. Evenson, Meagan M. Corliss, Lily Mahapatra, Ali Aldawood, David F. Carpentieri, Sarah L. Chamlin, Ann M. Kulungowski, Suneeta Madan-Khetarpal, Jessica Sebastian, Mitchell A. Pet, Carrie C. Coughlin, Marcia C. Willing, Gregory D. Pearson, Bhuvana A. Setty, Zaki El-Haffaf, Catherine E. Cottrell, Bijal A. Parikh, Kilannin Krysiak, Molly C. Schroeder, Jonathan W. Heusel, Julie A. Neidich, Yang Cao
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics.
RAS genes (HRAS, KRAS, and NRAS) are commonly mutated genes in cancer, and activating RAS variants are also found in disorders of somatic mosaicism (DoSM). A survey of the mutational spectrum of RAS variants in DoSM has not been performed.A total of
Publikováno v:
Pediatric and Developmental Pathology. 24:51-55
We describe a rare pediatric case of a phalangeal giant cell tumor of bone with extensive bilateral lung metastases following curettage, wide resection, and amputation. Concurrent peripheral blood eosinophilia and pleural effusion with marked eosinop
Autor:
Stephanie Fetzko, Adriana Fonseca, Mary Frances Wedekind, Abha A. Gupta, Bhuvana A. Setty, Jeremy Schraw, Philip J. Lupo, Robert P. Guillerman, Anish A. Butala, Heidi Russell, Lauren Nicholls, David Walterhouse, Douglas S. Hawkins, Mehmet F. Okcu
Publikováno v:
J Pediatr Hematol Oncol
BACKGROUND: We investigated whether surveillance imaging had an impact on post-relapse survival in patients with rhabdomyosarcoma (RMS). We hypothesized that relapse detected by imaging (group IM) would be associated with longer survival compared wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::717702605ecb478eb470e4a448eb3faa
https://europepmc.org/articles/PMC10026693/
https://europepmc.org/articles/PMC10026693/