Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Adriana Olar"'
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-9 (2020)
Abstract Glioblastoma is the most frequent and aggressive primary brain tumor, characterized by extensive brain invasion and rarely, systemic metastases. The pathogenesis of metastatic glioblastoma is largely unknown. We present the first integrated
Externí odkaz:
https://doaj.org/article/73bd1561f9134ed9868490394d54e43f
Autor:
Rachel Jester, Iya Znoyko, Maria Garnovskaya, Joseph N Rozier, Ryan Kegl, Sunil Patel, Tuan Tran, Malak Abedalthagafi, Craig M Horbinski, Mary Richardson, Daynna J Wolff, Razvan Lapadat, William Moore, Fausto J Rodriguez, Jason Mull, Adriana Olar
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-9 (2018)
Abstract Endolymphatic sac tumor (ELST) is a rare neoplasm arising in the temporal petrous region thought to originate from endolymphatic sac epithelium. It may arise sporadically or in association with Von-Hippel-Lindau syndrome (VHL). The ELST prev
Externí odkaz:
https://doaj.org/article/96d10438e2a9471eba63bc25a9fc4d64
Publikováno v:
Cancers, Vol 13, Iss 24, p 6218 (2021)
Ependymoma is a biologically diverse tumor wherein molecular classification has superseded traditional histological grading based on its superior ability to characterize behavior, prognosis, and possible targeted therapies. The current, updated molec
Externí odkaz:
https://doaj.org/article/aa51dc45fa3146e58266151ef1def069
Autor:
Maria-Magdalena Georgescu, Anil Nanda, Yan Li, Bret C. Mobley, Phyllis L. Faust, Jack M. Raisanen, Adriana Olar
Publikováno v:
Cancers, Vol 12, Iss 1, p 225 (2020)
Chordoid meningioma is a rare WHO grade II histologic variant. Its molecular alterations or their impact on patient risk stratification have not been fully explored. We performed a multicenter, clinical, histological, and genomic analysis of chordoid
Externí odkaz:
https://doaj.org/article/f46e9cbe82724453b368460ab606ca74
Autor:
Reid Trenton Powell, Adriana Olar, Shivali Narang, Ganesh Rao, Erik Sulman, Gregory N Fuller, Arvind Rao
Publikováno v:
Journal of Pathology Informatics, Vol 8, Iss 1, Pp 9-9 (2017)
Background: Glioma, the most common primary brain neoplasm, describes a heterogeneous tumor of multiple histologic subtypes and cellular origins. At clinical presentation, gliomas are graded according to the World Health Organization guidelines (WHO)
Externí odkaz:
https://doaj.org/article/b1a83111b9cd4216b8b283cdff1ab9a8
Autor:
Nimish A. Mohile, Hans Messersmith, Na Tosha Gatson, Andreas F. Hottinger, Andrew Lassman, Jordan Morton, Douglas Ney, Phioanh Leia Nghiemphu, Adriana Olar, Jeffery Olson, James Perry, Jana Portnow, David Schiff, Anne Shannon, Helen A. Shih, Roy Strowd, Martin van den Bent, Mateo Ziu, Jaishri Blakeley
Publikováno v:
Neuro Oncol
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 40(4), 403-426. American Society of Clinical Oncology
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 40(4), 403-426. American Society of Clinical Oncology
Purpose To provide guidance to clinicians regarding therapy for diffuse astrocytic and oligodendroglial tumors in adults. Methods ASCO and the Society for Neuro-Oncology convened an Expert Panel and conducted a systematic review of the literature. Re
Autor:
Annekathrin Reinhardt, Kristin Pfister, Daniel Schrimpf, Damian Stichel, Felix Sahm, David E. Reuss, David Capper, Annika K. Wefers, Azadeh Ebrahimi, Martin Sill, Joerg Felsberg, Guido Reifenberger, Albert Becker, Marco Prinz, Ori Staszewski, Christian Hartmann, Jens Schittenhelm, Dorothee Gramatzki, Michael Weller, Adriana Olar, Elisabeth Jane Rushing, Markus Bergmann, Michael A. Farrell, Ingmar Blümcke, Roland Coras, Jan Beckervordersandforth, Se Hoon Kim, Fabio Rogerio, Petia S. Dimova, Pitt Niehusmann, Andreas Unterberg, Michael Platten, Stefan M. Pfister, Wolfgang Wick, Christel Herold‐Mende, Andreas von Deimling
Publikováno v:
Neuropathology and Applied Neurobiology, 48(7):e12847. Wiley-Blackwell
Anaplastic ganglioglioma is a rare tumour, and diagnosis has been based on histological criteria. The 5th edition of the World Health Organization Classification of Tumours of the Central Nervous System (CNS WHO) does not list anaplastic gangliogliom
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-9 (2020)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Glioblastoma is the most frequent and aggressive primary brain tumor, characterized by extensive brain invasion and rarely, systemic metastases. The pathogenesis of metastatic glioblastoma is largely unknown. We present the first integrated clinical/
Autor:
Maria-Magdalena Georgescu, Gregory N. Fuller, Yan Li, Adriana Olar, Hai Sun, Mohammad Zahidul Islam, Christina Notarianni
Publikováno v:
Oncotarget
Epithelioid glioblastoma is a recognized glioblastoma variant, recently added to the World Health Organization brain tumor classification, with similar prognosis as the classic variant and B-Raf V600E mutations in 50% of the cases. We identified a ne
Autor:
Diep Tran, Suzanne Zein-Eldin Powell, Rajyalakshmi Luthra, Adriana Olar, Maria N. Garnovskaya, Gregory N. Fuller, Adekunle M. Adesina, Jawad Manekia, Vidya Mehta, Kenneth D. Aldape, Benjamin Ellezam, Erik P. Sulman, Carrie A. Mohila, Annekathrin Reinhardt, Gerald A. Campbell
Publikováno v:
Clinical Neuropathology. 38:59-73
Introduction Pilocytic astrocytoma (PA) with anaplastic features (PAAF) is a rare entity associated with decreased survival. It is characterized by hypercellularity, atypia, brisk mitotic activity, variable necrosis, and association with a classic PA