Zobrazeno 1 - 10
of 36
pro vyhledávání: '"S. Bulent Omay"'
Publikováno v:
AACE Clinical Case Reports, Vol 6, Iss 1, Pp e23-e29 (2020)
ABSTRACT: Objective: To describe a case of spontaneous resolution of primary hypercortisolism from Cushing disease (CD) due to pituitary apoplexy (PA). Methods: Clinical, laboratory, and pathologic information are described. Results: A 59-year-old fe
Externí odkaz:
https://doaj.org/article/1d02ce8cbe14416c8359c3c544ddc812
Publikováno v:
Journal of Neurosurgery: Case Lessons. 5
BACKGROUND Pituitary adenomas are the most common cause of pituitary enlargement and can potentially warrant surgical intervention. However, there are physiological causes of pituitary enlargement that can be reversed with hormone replacement alone.
Autor:
Brian Hilton, Olufisayo Adeyina, Kanat Yalcin, Christopher Hong, Zeynep Erson-Omay, S. Bulent Omay
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Autor:
Kanat Yalcin, Brian Hilton, Olufisayo Adeyina, Christopher Hong, S. Bulent Omay, Zeynep Erson-Omay
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Autor:
Murat Gunel, Zeynep Erson-Omay, Ketu Mishra-Gorur, Renelle Pointdujour-Lim, Arushii Nadar, Robert K. Fulbright, Lan Jin, Tanyeri Barak, Shaurey Vetsa, Evan Gorelick, Benjamin L. Judson, Jennifer Moliterno, Mariam Aboian, Michael Alperovich, Declan McGuone, S. Bulent Omay, Nicholas Blondin, Kanat Yalcin, Trisha P Gupte, Stephanie Aguilera, Mark W. Youngblood
Publikováno v:
Journal of Neuro-Oncology. 154:237-246
As sphenoid wing meningiomas (SWMs) are associated with varying degrees of bony involvement, we sought to understand potential relationships between genomic subgroup and this feature. Patients treated at Yale-New Haven Hospital for SWM were reviewed.
Publikováno v:
Journal of Neurosurgery: Case Lessons. 3
BACKGROUND Intracranial aneurysms and pituitary adenomas are relatively common pathologies that, in rare instances, may concurrently present. Their management poses considerable clinical and technical challenges. OBSERVATIONS The authors present a ca
Autor:
Christopher S. Hong, Yi An, Antonio Omuro, E. Zeynep Erson-Omay, Adeniyi Fisayo, Greg Fliney, Renelle Pointdujour-Lim, S. Bulent Omay, Pallavi P. Gopal
Publikováno v:
Brain Tumor Pathology
Optic nerve glioma (ONG) is a rare, typically slow-growing WHO I grade tumor that affects the visual pathways. ONG is most commonly seen in the pediatric population, in association with neurofibromatosis type 1 syndrome. However, sporadic adult cases
Autor:
Lan Jin, Shaurey Vetsa, Sagar Vasandani, Arushii Nadar, Mark W. Youngblood, Trisha Gupte, Tanyeri Barak, Kanat Yalcin, Stephanie Marie Aguilera, Ketu Mishra-Gorur, Nicholas A. Blondin, Evan Gorelick, S. Bulent Omay, Renelle Pointdujour-Lim, Benjamin L. Judson, Michael Alperovich, Mariam S. Aboian, Neelan Marianayagam, Declan McGuone, Murat Gunel, Zeynep Erson-Omay, Robert K. Fulbright, Jennifer Moliterno
Publikováno v:
31st Annual Meeting North American Skull Base Society.
Autor:
Christopher S, Hong, S Bulent, Omay
Publikováno v:
New England Journal of Medicine. 387:2366-2366
Publikováno v:
Neuro Oncol
Craniopharyngiomas arise from the embryonic remnants of Rathke’s pouch in the craniopharyngeal duct. Their invasive capacity and geographic proximity to the optic apparatus, pituitary gland and stalk, third ventricle, and the hypothalamus can cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb4cad706f82645d1a1022f1a9bedd56
https://europepmc.org/articles/PMC8598823/
https://europepmc.org/articles/PMC8598823/