Browsing NTNU Open by Author "Myren-Svelstad, Sverre"
Now showing items 1-7 of 7
-
Det bør hete St. Olav's University Hospital på engelsk
Myren-Svelstad, Sverre; Lohndal, Terje (Peer reviewed; Journal article, 2020) -
Early thrombectomy of a proximal middle cerebral artery occlusion leading to complete recovery with no infarct
Myren-Svelstad, Sverre; Hammer, Tommy Arild; Idicula, Titto (Journal article; Peer reviewed, 2017)Many recent trials show the benefit of mechanical thrombectomy in acute ischemic stroke caused by thrombi lodged in large arteries. We report the case of a 55-year-old patient who developed sudden-onset right-sided hemiplegia ... -
Epilepsy as a Network Disorder From Zebrafish to Humans
Myren-Svelstad, Sverre (Doctoral theses at NTNU;2022:217, Doctoral thesis, 2022) -
Glia-neuron interactions underlie state transitions to generalized seizures
Diaz Verdugo, Carmen; Myren-Svelstad, Sverre; Aydin, Ecem; Van Hoeymissen, Evelien; Deneubourg, Celine; Vanderhaeghe, Silke; Vancraeynest, Julie; Pelgrims, Robbrecht; Casacak, Mehmet Ilyas; Muto, Akira; Kawakami, Koichi; Jurisch-Yaksi, Nathalie; Yaksi, Emre (Journal article; Peer reviewed, 2019)Brain activity and connectivity alter drastically during epileptic seizures. The brain networks shift from a balanced resting state to a hyperactive and hypersynchronous state. It is, however, less clear which mechanisms ... -
Loss of glutamate transporter eaat2a leads to aberrant neuronal excitability, recurrent epileptic seizures, and basal hypoactivity
Hotz, Adriana L.; Jamali, Ahmed; Rieser, Nicolas N.; Niklaus, Stephanie; Aydin, Ecem; Myren-Svelstad, Sverre; Lalla, Laetitia Noelle Patricia; Jurisch-Yaksi, Nathalie; Yaksi, Emre; Neuhauss, Stephan C.F. (Peer reviewed; Journal article, 2021)Astroglial excitatory amino acid transporter 2 (EAAT2, GLT-1, and SLC1A2) regulates the duration and extent of neuronal excitation by removing glutamate from the synaptic cleft. Hence, an impairment in EAAT2 function could ... -
Remarkable effect of transdermal nicotine in children with CHRNA4- related autosomal dominant sleep-related hypermotor epilepsy
Lossius, Kristine; de Saint Martin, Anne; Myren-Svelstad, Sverre; Bjørnvold, Marit; Minken, Guro; Seegmuller, Caroline; Valenti Hirsch, Maria Paola; Chelly, Jamel; Steinlein, Ortrud; Picard, Fabienne; Brodtkorb, Eylert (Peer reviewed; Journal article, 2020)Objective Autosomal dominant sleep-related hypermotor epilepsy (ADSHE) is characterized by hypermotor seizures and may be caused by gain-of-function mutations affecting the nicotinic acetylcholine receptor (nAChR). Benefit ... -
The spectrum of pyridoxine dependent epilepsy across the age span: A nationwide retrospective observational study
Jamali, Ahmed; Kristensen, Erle; Tangeraas, Trine; Arntsen, Vibeke; Sikric, Alma; Kupliauskiene, Guste; Myren-Svelstad, Sverre; Berland, Siren; Sejersted, Yngve; Gerstner, Thorsten Alfons; Hassel, Bjørnar; Bindoff, Laurence Albert; Brodtkorb, Eylert August (Peer reviewed; Journal article, 2023)Background Pyridoxine-dependent epilepsy (PDE) is a rare seizure disorder usually presenting with neonatal seizures. Most cases are caused by biallelic pathogenic ALDH7A1variants. While anti-seizure medications are ...