Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Thomas M Pearce"'
Autor:
Juan C. Vizcarra, Thomas M. Pearce, Brittany N. Dugger, Michael J. Keiser, Marla Gearing, John F. Crary, Evan J. Kiely, Meaghan Morris, Bartholomew White, Jonathan D. Glass, Kurt Farrell, David A. Gutman
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-20 (2023)
Abstract Machine learning (ML) has increasingly been used to assist and expand current practices in neuropathology. However, generating large imaging datasets with quality labels is challenging in fields which demand high levels of expertise. Further
Externí odkaz:
https://doaj.org/article/b2678bd5981b4644b024934250897893
Autor:
Manuel Paez-Escamilla, Sonny Caplash, Gagan Kalra, Jamie Odden, Danielle Price, Oscar C. Marroquin, Stephen Koscumb, Patrick Commiskey, Chad Indermill, Jerome Finkelstein, Anna G. Gushchin, Andreea Coca, Thomas R. Friberg, Andrew W. Eller, Denise S. Gallagher, Jean C. Harwick, Evan L. Waxman, Jay Chhablani, Gabrielle Bonhomme, Colin Prensky, Alexander J. Anetakis, Joseph N. Martel, Erika Massicotte, Raphaelle Ores, Jean-Francois Girmens, Thomas M Pearce, Jose-Alain Sahel, Kunal Dansingani, Mark Westcott, Marie-Helene Errera
Publikováno v:
Journal of Ophthalmic Inflammation and Infection, Vol 13, Iss 1, Pp 1-27 (2023)
Abstract Purpose Posterior uveitis is a common chorioretinal pathology affecting all ages worldwide and is a frequent reason for referral to the retina clinic. The spectrum of etiologies for uveitis is very broad and includes infectious and auto-immu
Externí odkaz:
https://doaj.org/article/79ccda5d6777489f838edc6d62520dfd
Autor:
Zachary C. Gersey, Kenan R. Rajjoub, Thomas M. Pearce, Scott A. Segel, Paul A. Gardner, Carl H. Snyderman, Eric W. Wang, Georgios A. Zenonos
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Abstract Background Immunoglobulin-G4-related hypophysitis is a rare inflammatory disease that can present as a tumefactive pituitary lesion mimicking hypophyseal neoplasms such as pituitary adenoma or craniopharyngioma. The literature on this entity
Externí odkaz:
https://doaj.org/article/fb6a55e0afee49dea414ff0fc491c143
Autor:
Daniel F. Marker, Thomas M. Pearce
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Abstract IDH-mutant astrocytomas have a more indolent natural history and better prognosis than their IDH-wild type counterparts, but are still graded according to schemes developed prior to the recognition of this type of neoplasm as a distinct enti
Externí odkaz:
https://doaj.org/article/38134909ea4f40d69154bc8c608a2a43
Autor:
Daniel F. Marker, Thomas M. Pearce
Publikováno v:
Seminars in Diagnostic Pathology. 40:47-51
Germ cell tumors of the central nervous system (GCT-CNS) arise predominantly in midline locations of the CNS and affect young patients in their first to third decades of life. Involvement of the CNS is thought to be a sequelae of residual primordial
Autor:
Michal Nisnboym Ziv, Sarah R. Vincze, Itay Raphael, Zujian Xiong, Chaim T. Sneiderman, Rebecca A. Raphael, Bo Li, Ambika P. Jaswal, ReidAnn Sever, Kathryn E. Day, Joseph D. LaToche, Lesley M. Foley, T. Kevin Hitchens, Sameer Agnihotri, Baoli Hu, Dhivyaa Rajasundaram, Carolyn J. Anderson, Deborah T. Blumenthal, Thomas M. Pearce, Shikhar Uttam, Jessie R. Nedrow, Ashok Panigrahy, Ian F. Pollack, Frank S. Lieberman, Jan Drappatz, Wilson B. Edwards, Gary Kohanbash
Publikováno v:
Monday, April 24.
Autor:
Carl H. Snyderman, Zachary C. Gersey, Georgios A. Zenonos, Paul A. Gardner, Eric W. Wang, Kenan R. Rajjoub, Scott A. Segel, Thomas M. Pearce
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Immunoglobulin-G4-related hypophysitis is a rare inflammatory disease that can present as a tumefactive pituitary lesion mimicking hypophyseal neoplasms such as pituitary adenoma or craniopharyngioma. The literature on this entity is spars
Autor:
Angelica Zin, Sarangarajan Ranganathan, Barbara Cafferata, Mariarita Santi, Evelina Miele, Scott M. Kulich, Kelly M. Bailey, Sabrina Rossi, MacLean P Nasrallah, Marilyn M. Li, Yiming Zhong, Rita Alaggio, Thomas M. Pearce, Lea F Surrey, Oscar Lopez-Nunez, Alberto Broniscer
Publikováno v:
Brain Pathology
The group of CNS mesenchymal (non‐meningothelial) and primary glial/neuronal tumors in association with EWSR1‐non‐ETS rearrangements comprises a growing spectrum of entities, mostly reported in isolation with incomplete molecular profiling. Arc
Autor:
Thomas M. Pearce, Michael M. McDowell, Hussein M. Abdallah, Nallammai Muthiah, Eric W. Wang, Zachary C. Gersey, Carl H. Snyderman, Paul A. Gardner, Georgios A. Zenonos, Tina Costacou
Publikováno v:
J Neurol Surg B Skull Base
Objective Previous work categorized skull base chordoma (SBC) into three genetic risk groups based on 1p36 and homozygous 9p21(p16) deletions, accounting for a wide variability in prognosis (A = low-risk, B = intermediate-risk, C = high-risk). Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86c34f17243fcf8fae47c761be1eb73
https://europepmc.org/articles/PMC8563266/
https://europepmc.org/articles/PMC8563266/
Publikováno v:
Pediatric Neurosurgery. 54:347-353
Translocations between EWSR1 and members of the CREB family of transcription factors (CREB1, ATF1, and CREM) are rare genetic findings occurring in various sarcomas. Of these, the EWSR1-CREM translocation is the most rarely reported. We present the c