Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Steven N, Roper"'
Autor:
Lindsey F. Jackson, Jennifer K. Mulligan, Jeb M. Justice, Steven N. Roper, Jason E. Blatt, Brian C. Lobo
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Autor:
Steven N. Roper, Maryam Rahman, Aida Karachi, David Shin, Paul Kubilis, Brian L. Hoh, Alexander L. Vlasak
Publikováno v:
World Neurosurgery. 135:e510-e519
Patient safety indicators (PSIs) and hospital-acquired conditions (HACs) are reported quality measures. We compared their prevalence in patients with secretory and nonsecretory pituitary adenoma using the National (Nationwide) Inpatient Sample (NIS),
Autor:
Steven N. Roper
Publikováno v:
EBioMedicine, Vol 7, Iss C, Pp 19-20 (2016)
Externí odkaz:
https://doaj.org/article/ce4021d4edcd485390651e0588ffbc68
Autor:
Fu-Wen Zhou, Jeff M Fortin, Huan-Xin Chen, Hildabelis Martinez-Diaz, Lung-Ji Chang, Brent A Reynolds, Steven N Roper
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120281 (2015)
This study investigates the electrophysiological properties and functional integration of different phenotypes of transplanted human neural precursor cells (hNPCs) in immunodeficient NSG mice. Postnatal day 2 mice received unilateral injections of 10
Externí odkaz:
https://doaj.org/article/5ebcc3c978e24e0eb3d2e2cd91490385
Autor:
Fumiaki Yokoi, Huan-Xin Chen, Mai Tu Dang, Chad C Cheetham, Susan L Campbell, Steven N Roper, J David Sweatt, Yuqing Li
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120916 (2015)
DYT1 dystonia is an inherited movement disorder caused by mutations in DYT1 (TOR1A), which codes for torsinA. Most of the patients have a trinucleotide deletion (ΔGAG) corresponding to a glutamic acid in the C-terminal region (torsinA(ΔE)). Dyt1 Δ
Externí odkaz:
https://doaj.org/article/f358a7afcaec458fbca1b68aab27d38b
Autor:
Mark P DeAndrade, Li Zhang, Atbin Doroodchi, Fumiaki Yokoi, Chad C Cheetham, Huan-Xin Chen, Steven N Roper, J David Sweatt, Yuqing Li
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35518 (2012)
Polymorphisms in BTBD9 have recently been associated with higher risk of restless legs syndrome (RLS), a neurological disorder characterized by uncomfortable sensations in the legs at rest that are relieved by movement. The BTBD9 protein contains a B
Externí odkaz:
https://doaj.org/article/38820f198fbe4df78498e134850cb750
Autor:
Steven N. Roper, Erik H. Middlebrooks, Thomas H. Mareci, Michael A. King, Ronald G. Quisling, Paul R. Carney, Luis M. Colon-Perez
Publikováno v:
Surgical and Radiologic Anatomy. 39:1149-1159
The hippocampus has a critical role in many common disease processes. Currently, routine 3 Tesla structural MRI is a mainstay of clinical diagnosis. The goal of our study is to evaluate the normal variability in size and/or conspicuity of the hippoca
Publikováno v:
Journal of the Endocrine Society
Background: Pituitary apoplexy (PA) is a relatively rare condition associated with sudden hemorrhagic pituitary infarction, and usually occurs in the setting of a pituitary adenoma. Patients typically present with the acute onset of headache, visual
Autor:
William S Dodd, Rachel Moor, Ashley Ghiaseddin, Anthony T. Yachnis, Samuel L. Malnik, David Shin, W. Christopher Fox, Jorge A. Trejo-Lopez, Dimitri Laurent, Steven N. Roper
Publikováno v:
Surgical Neurology International
Background: Inflammatory myofibroblastic tumor is a rare, poorly understood tumor that has been found to occur in almost every organ tissue. Its location within the central nervous system is uncommon, and patients tend to present with nonspecific sym
Autor:
Michael Wong, Steven N. Roper
Publikováno v:
Journal of Neuroscience Methods. 260:73-82
Malformations of cortical development constitute a variety of pathological brain abnormalities that commonly cause severe, medically-refractory epilepsy, including focal lesions, such as focal cortical dysplasia, hetereotopias, and tubers of tuberous