Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Oliver D Mrowczynski"'
Autor:
A B Madhankumar, Oliver D Mrowczynski, Becky Slagle-Webb, Vagisha Ravi, Alexandre J Bourcier, Russell Payne, Kimberly S Harbaugh, Elias Rizk, James R Connor
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0181529 (2018)
Peripheral nerve sheath tumors are benign tumors that have the potential to transform into malignant peripheral nerve sheath tumors (MPNSTs). Interleukin-13 receptor alpha 2 (IL13Rα2) is a cancer associated receptor expressed in glioblastoma and oth
Externí odkaz:
https://doaj.org/article/3d581631ae1648e8b5e675d0ea7384cd
Autor:
Kristin K Howell, Bradley R Monk, Stephanie A Carmack, Oliver D Mrowczynski, Robert E Clark, Stephan G Anagnostaras
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 8 (2014)
The atypical PKC isoforms, PKMζ and PKCλ have been proposed as integral substrates of long-term memory. Inhibition of these isoforms has recently been demonstrated to be sufficient for impairing the expression and maintenance of long-term potentiat
Externí odkaz:
https://doaj.org/article/7dc214e889424f378342f51a77547bf7
Autor:
Oliver D. Mrowczynski, Dawit Aregawi, Elias Rizk, Christine Mau, Ganesh Shenoy, Vladimir Khristov, Cunfeng Pu, Charles S. Specht
Publikováno v:
World Neurosurgery. 158:e735-e745
Background Myxopapillary ependymomas (MPE) with anaplastic features are rarely reported with only 21 cases identified to date, and long-term recurrence is rarely presented. The purpose of this case series is to expand understanding of this disease by
Publikováno v:
Cureus.
Autor:
Robert J. Greiner, Elias Rizk, Oliver D. Mrowczynski, Charles S. Specht, Mark Iantosca, Jessica Lane
Publikováno v:
Child's Nervous System. 36:2845-2849
Intracranial ganglioneuroblastomas are incredibly rare neuroectodermal tumors with only 8 described cases total, 5 of those having imaging findings METHODS: Here we present a 9-year-old female patient with 4 months progressive headaches, personality
Autor:
Colette R. Pameijer, Nicholas G. Zaorsky, Oliver D. Mrowczynski, Kimberly Harbaugh, Monali Vasekar, Russell Payne, Dawit Aregawi, Edward Fox, Elias Rizk
Publikováno v:
Cureus
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders. It can cause plexiform neurofibromas, leading to diffuse enlargement of a nerve or nerves within the body. There are benign in general, however, can cause sign
Autor:
James R. Connor, A. B. Madhankumar, Alexandre J. Bourcier, Christine Mau, Darren Wolfe, Elias Rizk, Oliver D. Mrowczynski, Kimberly Harbaugh, Becky Slagle-Webb, Stephan B. Abramson, Russell Payne, Ganesh Shenoy
Publikováno v:
Journal of Neurosurgery. 131:1369-1379
OBJECTIVEMalignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas that harbor a high potential for metastasis and have a devastating prognosis. Combination chemoradiation aids in tumor control and decreases tumor recurren
Autor:
Jason Liao, Alexandre J. Bourcier, Elias Rizk, Samer G. Zammar, Oliver D. Mrowczynski, Sara T. Langan, Charles S. Specht
Publikováno v:
World Neurosurgery. 120:e1171-e1174
Background The standard of care for glioblastoma is surgical resection followed by combination temozolomide and radiation. Magnetic resonance imaging (MRI) is used preoperatively for tumor resection planning. In some instances, MRI is also obtained p
Publikováno v:
Cureus
Glioblastoma is a devastating malignancy with a dismal survival rate and median survival time of 14 months. Currently, the biomarkers for glioblastoma are mostly molecular and include EGFRvIII, ATRX, PTEN, IDH1, MGMT, and others. These prognostic tum
PurposeGlioblastoma is a devastating malignancy with a dismal survival rate and median survival time of 14 months. Currently, the biomarkers for glioblastoma are mostly molecular and include EGFRvIII, ATRX, PTEN, IDH1, MGMT, and others. These prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9db4bb7732bdee8efc6e4f9e884c865c
https://doi.org/10.21203/rs.3.rs-200717/v1
https://doi.org/10.21203/rs.3.rs-200717/v1