Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Anne E, Anderson"'
Publikováno v:
Epilepsia Open, Vol 6, Iss 3, Pp 588-596 (2021)
Abstract Objective Cardiac alterations represent a potential epilepsy‐associated comorbidity. Whether cardiac changes occur as a function of epilepsy duration is not well understood. We sought to evaluate whether cardiac alterations represented a t
Externí odkaz:
https://doaj.org/article/a7cbcac4f5374ad48883b2ad16c77c9b
Autor:
Elizabeth L. Berg, Stela P. Petkova, Heather A. Born, Anna Adhikari, Anne E. Anderson, Jill L. Silverman
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-16 (2021)
Abstract Background Angelman Syndrome (AS) is a rare neurodevelopmental disorder for which there is currently no cure or effective therapeutic. Since the genetic cause of AS is known to be dysfunctional expression of the maternal allele of ubiquitin
Externí odkaz:
https://doaj.org/article/248aa6f6f0a749df873e2e42f60659e7
Synapse-specific changes in Arc and BDNF in rat hippocampus following chronic temporal lobe epilepsy
Publikováno v:
Neuroscience Research. 191:1-12
Expression of immediate early genes (IEGs) in the brain is important for synaptic plasticity, and probably also in neurodegenerative conditions. To understand the cellular mechanisms of the underlying neuropathophysiological processes in epilepsy, we
Autor:
Lena H. Nguyen, Anne E. Anderson
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Abstract Cortical dysplasia (CD) is a common cause for intractable epilepsy. Hyperactivation of the mechanistic target of rapamycin (mTOR) pathway has been implicated in CD; however, the mechanisms by which mTOR hyperactivation contribute to the epil
Externí odkaz:
https://doaj.org/article/3e4b16d953fe499aab83dde480dccf15
Autor:
Heather A. Born, An T. Dao, Amber T. Levine, Wai Ling Lee, Natasha M. Mehta, Shubhangi Mehra, Edwin J. Weeber, Anne E. Anderson
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Angelman syndrome (AS) is a genetic neurodevelopmental disorder, most commonly caused by deletion or mutation of the maternal allele of the UBE3A gene, with behavioral phenotypes and seizures as key features. Currently no treatment is availa
Externí odkaz:
https://doaj.org/article/f0286cef58f8494082fc0f0267c3148a
Autor:
Carlos J. Ballester‐Rosado, John T. Le, Trang T. Lam, Carrie A. Mohila, Sandi Lam, Anne E. Anderson, James D. Frost, John W. Swann
Publikováno v:
Annals of Neurology. 92:45-60
Autor:
Heather A. Born, Lena H. Nguyen, Youfen Xu, Travorn Mahadeo, Angélique Bordey, Tiffany V. Lin, Anne E. Anderson, Longbo Zhang
Publikováno v:
Brain
Hyperactivation of the mTOR pathway during foetal neurodevelopment alters neuron structure and function, leading to focal malformation of cortical development and intractable epilepsy. Recent evidence suggests a role for dysregulated cap-dependent tr
Autor:
Raquel Farias-Moeller, Ravindra Arya, Katrina Peariso, Joshua L. Goldstein, Eric T. Payne, Yi-Chen Lai, Bo Zhang, Mohamad A. Mikati, Latania Reece, Tobias Loddenkemper, Angus Wilfong, Korwyn Williams, Brian Appavu, Robert C. Tasker, Juan Piantino, Marina Gaínza-Lein, William D. Gaillard, Tiffani L McDonough, James J. Riviello, Cristina Barcia Aguilar, Kush Kapur, Justice Clark, Howard P. Goodkin, Tristan T. Sands, Theodore Sheehan, Kevin E. Chapman, Jessica L. Carpenter, Edward J. Novotny, Robert J. Kahoud, James Nicholas Brenton, Iván Sánchez Fernández, Dmitry Tchapyjnikov, Kumar Sannagowdara, Anne E. Anderson, Marta Amengual-Gual, Mark S. Wainwright, Tracy A. Glauser, Lindsey A. Morgan, Anuranjita Nayak, Adam P. Ostendorf, Linda Huh, Alejandra Vasquez
Publikováno v:
Epilepsia. 62:2190-2204
Objective This study was undertaken to describe long-term clinical and developmental outcomes in pediatric refractory status epilepticus (RSE) and identify factors associated with new neurological deficits after RSE. Methods We performed retrospectiv
Autor:
Isabella G. Febbo, Luis A. Martinez, Valerie Warkins, Nadia Vargas, Anne E. Anderson, Laura A. Schrader
Publikováno v:
The FASEB Journal. 36
Autor:
Edwin J. Weeber, Joseph C. Grieco, Sarah E. Harris, Heather A. Born, Angelique Regnier-Golanov, Luis A. Martinez, Anne E. Anderson
Publikováno v:
Clinical EEG and Neuroscience. 54:203-212
The goal of these studies was to use quantitative (q)EEG techniques on data from children with Angelman syndrome (AS) using spectral power analysis, and to evaluate this as a potential biomarker and quantitative method to evaluate therapeutics. Altho