Zobrazeno 1 - 10
of 799
pro vyhledávání: '"Ulrich Stephani"'
Autor:
Dennis Lal, Ann-Kathrin Ruppert, Holger Trucks, Herbert Schulz, Carolien G de Kovel, Dorothée Kasteleijn-Nolst Trenité, Anja C M Sonsma, Bobby P Koeleman, Dick Lindhout, Yvonne G Weber, Holger Lerche, Claudia Kapser, Christoph J Schankin, Wolfram S Kunz, Rainer Surges, Christian E Elger, Verena Gaus, Bettina Schmitz, Ingo Helbig, Hiltrud Muhle, Ulrich Stephani, Karl M Klein, Felix Rosenow, Bernd A Neubauer, Eva M Reinthaler, Fritz Zimprich, Martha Feucht, Rikke S Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, Wolfgang Lieb, Andre Franke, Konstantin Strauch, Christian Gieger, Claudia Schurmann, Ulf Schminke, Peter Nürnberg, EPICURE Consortium, Thomas Sander
Publikováno v:
PLoS Genetics, Vol 11, Iss 5, p e1005226 (2015)
Genetic generalised epilepsy (GGE) is the most common form of genetic epilepsy, accounting for 20% of all epilepsies. Genomic copy number variations (CNVs) constitute important genetic risk factors of common GGE syndromes. In our present genome-wide
Externí odkaz:
https://doaj.org/article/7a9aaf42fe42407c9b6b46e8e6a9130a
Autor:
Natia Japaridze, Muthuraman Muthuraman, Christine Reinicke, Friederike Moeller, Abdul Rauf Anwar, Kidist Gebremariam Mideksa, Ronit Pressler, Günther Deuschl, Ulrich Stephani, Michael Siniatchkin
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0123807 (2015)
Burst-suppression (BS) is an electroencephalography (EEG) pattern consisting of alternant periods of slow waves of high amplitude (burst) and periods of so called flat EEG (suppression). It is generally associated with coma of various etiologies (hyp
Externí odkaz:
https://doaj.org/article/c95921258d4d4236a576a996ef215395
Autor:
Muthuraman Muthuraman, Vera Moliadze, Kidist Gebremariam Mideksa, Abdul Rauf Anwar, Ulrich Stephani, Günther Deuschl, Christine M Freitag, Michael Siniatchkin
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0140832 (2015)
At the sensor level many aspects, such as spectral power, functional and effective connectivity as well as relative-power-ratio ratio (RPR) and spatial resolution have been comprehensively investigated through both electroencephalography (EEG) and ma
Externí odkaz:
https://doaj.org/article/b124031eb04e4a0aa8658c747d40a8bc
Autor:
Peter Neal Taylor, Yujiang Wang, Marc Goodfellow, Justin Dauwels, Friederike Moeller, Ulrich Stephani, Gerold Baier
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e114316 (2014)
Active brain stimulation to abate epileptic seizures has shown mixed success. In spike-wave (SW) seizures, where the seizure and background state were proposed to coexist, single-pulse stimulations have been suggested to be able to terminate the seiz
Externí odkaz:
https://doaj.org/article/d8fde66ad3c14eb584ea1485a0a3f6f5
Autor:
Lydia Elshoff, Muthuraman Muthuraman, Abdul Rauf Anwar, Günther Deuschl, Ulrich Stephani, Jan Raethjen, Michael Siniatchkin
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e78422 (2013)
The concept of focal epilepsies includes a seizure origin in brain regions with hyper synchronous activity (epileptogenic zone and seizure onset zone) and a complex epileptic network of different brain areas involved in the generation, propagation, a
Externí odkaz:
https://doaj.org/article/14d6cbd85408439aaea08ba3076d9d04
Autor:
Heather C Mefford, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Karen Buysse, Carl Baker, Andre Franke, Alain Malafosse, Pierre Genton, Pierre Thomas, Christina A Gurnett, Stefan Schreiber, Alexander G Bassuk, Michel Guipponi, Ulrich Stephani, Ingo Helbig, Evan E Eichler
Publikováno v:
PLoS Genetics, Vol 6, Iss 5, p e1000962 (2010)
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a lifetime incidence of 3%. Several genes have been identified in rare autosomal dominant and severe sporadic forms of epilepsy, but the genetic cause is
Externí odkaz:
https://doaj.org/article/4c7d34241c57480e97451c913cdc2619
Publikováno v:
Seizure. 103:101-107
This prospective observational study evaluated the long-term EEG changes in children treated with everolimus (EVO) for refractory TSC-associated epilepsy. Changes in EEG-abnormalities were related to developmental outcomes.Thirteen children treated w
Publikováno v:
Clinical Neurophysiology. 132:2222-2231
Objective Childhood absence epilepsy (CAE) is a disease with distinct seizure semiology and electroencephalographic (EEG) features. Differentiating ictal and subclinical generalized spikes and waves discharges (GSWDs) in the EEG is challenging, since
Publikováno v:
Journal of neurology.
Childhood absence epilepsy (CAE), involves 3 Hz generalized spikes and waves discharges (GSWDs) on the electroencephalogram (EEG), associated with ictal discharges (seizures) with clinical symptoms and impairment of consciousness and subclinical disc
Autor:
Ulrich Stephani
Bericht über den Vortrag Jördis Frommholds, die im Rahmen der Ringvorlesung Die Coronavirus-Pandemie und ihre Folgen II der Christian-Albrechts-Universität zu Kiel über Rehabilitationserfahrungen und -Erkenntnisse aus Ihrer Arbeit mit Patient*inn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76017a77cc33b71d50f72ca574ce4f49
https://doi.org/10.38072/978-3-928794-82-4/p6
https://doi.org/10.38072/978-3-928794-82-4/p6