Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Elaine Hughes"'
Autor:
Ioannis Stavropoulos, Richard Selway, Harutomo Hasegawa, Elaine Hughes, Chris Rittey, Diego Jiménez-Jiménez, Antonio Valentin
Publikováno v:
Brain Stimulation, Vol 14, Iss 2, Pp 226-229 (2021)
Externí odkaz:
https://doaj.org/article/0f28445014da474b87aca24d6e4db167
Autor:
Laura B. Jones, Colin H. Peters, Richard E. Rosch, Maxine Owers, Elaine Hughes, Deb K. Pal, Peter C. Ruben
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Variants of the SCN1A gene encoding the neuronal voltage-gated sodium channel NaV1.1 cause over 85% of all cases of Dravet syndrome, a severe and often pharmacoresistent epileptic encephalopathy with mostly infantile onset. But with the increased ava
Externí odkaz:
https://doaj.org/article/ec6ce9af36bc4a238ada273bf434f84e
Autor:
Costin Leu, Simona Balestrini, Bridget Maher, Laura Hernández-Hernández, Padhraig Gormley, Eija Hämäläinen, Kristin Heggeli, Natasha Schoeler, Jan Novy, Joseph Willis, Vincent Plagnol, Rachael Ellis, Eleanor Reavey, Mary O'Regan, William O. Pickrell, Rhys H. Thomas, Seo-Kyung Chung, Norman Delanty, Jacinta M. McMahon, Stephen Malone, Lynette G. Sadleir, Samuel F. Berkovic, Lina Nashef, Sameer M. Zuberi, Mark I. Rees, Gianpiero L. Cavalleri, Josemir W. Sander, Elaine Hughes, J. Helen Cross, Ingrid E. Scheffer, Aarno Palotie, Sanjay M. Sisodiya
Publikováno v:
EBioMedicine, Vol 2, Iss 9, Pp 1063-1070 (2015)
Sudden unexpected death in epilepsy (SUDEP) represents the most severe degree of the spectrum of epilepsy severity and is the commonest cause of epilepsy-related premature mortality. The precise pathophysiology and the genetic architecture of SUDEP r
Externí odkaz:
https://doaj.org/article/c17cbb036c8f454c88b34a60b24d288b
Autor:
Daniel Bertrand, Frances Elmslie, Elaine Hughes, John Trounce, Thomas Sander, Sonia Bertrand, Ortrud K. Steinlein
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 3, Pp 799-804 (2005)
Mutations in nAChRs are found in a rare form of nocturnal frontal lobe epilepsy (ADNFLE). Previously, some nAChR mutations have been described that are associated with additional neurological features such as psychiatric disorders or cognitive defect
Externí odkaz:
https://doaj.org/article/44e0c960763041c58cbf7df05fa4f261
Publikováno v:
Seizure. 103:46-50
Quinidine has been proposed as a repurposed licensed drug for the treatment of seizures in KCNT1 gain-of-function associated Epilepsy of Infancy with Migrating Focal Seizures (EIMFS). Sparse evidence from case reports suggests limited effectiveness a
Autor:
Elaine Hughes, Chris Rittey, Antonio Valentin, Richard Selway, Harutomo Hasegawa, Ioannis Stavropoulos, Diego Jiménez-Jiménez
Publikováno v:
Brain Stimulation, Vol 14, Iss 2, Pp 226-229 (2021)
Autor:
Ben Donovan, Samantha Ashby, Jane Hanna, Tracy Cowdry, Jennifer Thorpe, Elaine Hughes, Mike P. Kerr, Rhys H. Thomas
Publikováno v:
Epilepsy & Behavior. 139:109071
Autor:
Donald P. Craig, Yun Young Choi, Rhys H. Thomas, Karen Osland, Michael Patrick Kerr, Elaine Hughes, Jane Hanna
Publikováno v:
Acta Neurologica Scandinavica. 143:509-513
Background Sudden unexpected death in epilepsy (SUDEP) accounts for a large percentage of deaths in children with epilepsy. Contributing factors to paediatric SUDEP are incompletely understood. Aims of study The Epilepsy Deaths Register (EDR) is an a
Autor:
Elaine Hughes
Publikováno v:
Collections: A Journal for Museum and Archives Professionals. 17:46-53
The Museum of Northern Arizona (MNA) is a private institution yet an estimated 89 percent of its archaeological holdings are not owned by the museum. The story of how MNA acquired these collections is rooted in its founding in 1928 by a group of loca
Autor:
Elaine Hughes
Publikováno v:
Collections: A Journal for Museum and Archives Professionals. 16:344-354
The use of an education collection in nontraditional museum settings is presented as a case study based on work at the Museum of Northern Arizona (MNA) between 2004 and 2020. MNA sought to resolve the use of permanent collections in nontraditional mu