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Fletta eftir efnisorði "Neurology"

Fletta eftir efnisorði "Neurology"

Röðun: Raða: Niðurstöður:

  • Jacob, Deborah; Guerrini, Lorena; Pescaglia, Federica; Pierucci, Simona; Gelormini, Carmine; Minutolo, Vincenzo; Fratini, Antonio; Di Lorenzo, Giorgio; Petersen, Hannes; Gargiulo, Paolo (2023)
    INTRODUCTION: There is accumulating evidence that many pathological conditions affecting human balance are consequence of postural control (PC) failure or overstimulation such as in motion sickness. Our research shows the potential of using the response ...
  • Kristinsson, Sigfús Helgi; Busby, Natalie; Rorden, Christopher; Newman-Norlund, Roger; Den Ouden, Dirk B.; Magnúsdóttir, Sigríður; Hjaltason, Haukur; Thors, Helga; Hillis, Argye E.; Kjartansson, Olafur; Bonilha, Leonardo; Fridriksson, Julius (2022)
    The association between age and language recovery in stroke remains unclear. Here, we used neuroimaging data to estimate brain age, a measure of structural integrity, and examined the extent to which brain age at stroke onset is associated with (i) ...
  • Nardone, Raffaele; Golaszewski, Stefan; Schwenker, Kerstin; Brigo, Francesco; Maccarrone, Miriam; Versace, Viviana; Sebastianelli, Luca; Saltuari, Leopold; Höller, Yvonne (2019-08-01)
    The pathophysiological mechanisms of cognitive and gait disturbances in subjects with normal-pressure hydrocephalus (NPH) are still unclear. Cholinergic and other neurotransmitter abnormalities have been reported in animal models of NPH. The objective ...
  • Cohen, Jacqueline M.; Alvestad, Silje; Cesta, Carolyn E.; Bjørk, Marte Helene; Leinonen, Maarit K.; Nørgaard, Mette; Einarsdóttir, Kristjana; Engeland, Anders; Gissler, Mika; Karlstad, Øystein; Klungsøyr, Kari; Odsbu, Ingvild; Reutfors, Johan; Selmer, Randi M.; Tomson, Torbjörn; Ulrichsen, Sinna Pilgaard; Zoega, Helga; Furu, Kari (2022-12-12)
    Objective: This study was undertaken to examine the comparative safety of antiseizure medication (ASM) monotherapy in pregnancy with respect to risk of major congenital malformations (MCMs), overall and by MCM subtype. Methods: We conducted a ...
  • Somaskandhan, Pranavan; Leppänen, Timo; Terrill, Philip I; Sigurdardottir, Sigridur; Arnardóttir, Erna Sif; Ólafsdóttir, Kristín Anna; Serwatko, Marta; Sigurðardóttir, Sigurveig Þ; Clausen, Michael Valur; Töyräs, Juha; Korkalainen, Henri (2023-04-14)
    INTRODUCTION: Visual sleep scoring has several shortcomings, including inter-scorer inconsistency, which may adversely affect diagnostic decision-making. Although automatic sleep staging in adults has been extensively studied, it is uncertain whether ...
  • Kristjansson, Arni; Moldoveanu, Alin; Jóhannesson, Ómar I.; Bălan, Oana; Spagnol, Simone; Valgeirsdóttir, Vigdís Vala; Unnthorsson, Runar (IOS Press, 2016-09-21)
    An exciting possibility for compensating for loss of sensory function is to augment deficient senses by conveying missing information through an intact sense. Here we present an overview of techniques that have been developed for sensory substitution ...
  • McCormack, Mark; Gui, Hongsheng; Ingason, Andrés; Speed, Doug; Wright, Galen E.B.; Zhang, Eunice J.; Secolin, Rodrigo; Yasuda, Clarissa; Kwok, Maxwell; Wolking, Stefan; Becker, Felicitas; Rau, Sarah; Avbersek, Andreja; Heggeli, Kristin; Leu, Costin; Depondt, Chantal; Sills, Graeme J.; Marson, Anthony G.; Auce, Pauls; Brodie, Martin J.; Francis, Ben; Johnson, Michael R.; Koeleman, Bobby P.C.; Striano, Pasquale; Coppola, Antonietta; Zara, Federico; Kunz, Wolfram S.; Sander, Josemir W.; Lerche, Holger; Klein, Karl Martin; Weckhuysen, Sarah; Krenn, Martin; Gudmundsson, Lárus J.; Stefansson, Kari; Krause, Roland; Shear, Neil; Ross, Colin J.D.; Delanty, Norman; Pirmohamed, Munir; Carleton, Bruce C.; Cendes, Fernando; Lopes-Cendes, Iscia; Liao, Wei-ping; O'Brien, Terence J.; Sisodiya, Sanjay M.; Cherny, Stacey; Kwan, Patrick; Baum, Larry; Cavalleri, Gianpiero L. (Ovid Technologies (Wolters Kluwer Health), 2017-12-29)
    Objective To characterize, among European and Han Chinese populations, the genetic predictors of maculopapular exanthema (MPE), a cutaneous adverse drug reaction common to antiepileptic drugs. Methods We conducted a case-control genome-wide association ...
  • van der Lee, Sven J.; Knol, Maria J.; Chauhan, Ganesh; Satizabal, Claudia L.; Smith, Albert Vernon; Hofer, Edith; Bis, Joshua C.; Hibar, Derrek P.; Hilal, Saima; van den Akker, Erik B.; Arfanakis, Konstantinos; Bernard, Manon; Yanek, Lisa R.; Amin, Najaf; Crivello, Fabrice; Cheung, Josh W.; Harris, Tamara B.; Saba, Yasaman; Lopez, Oscar L.; Li, Shuo; van der Grond, Jeroen; Yu, Lei; Paus, Tomas; Roshchupkin, Gennady V.; Amouyel, Philippe; Jahanshad, Neda; Taylor, Kent D.; Yang, Qiong; Mathias, Rasika A.; Boehringer, Stefan; Mazoyer, Bernard; Rice, Ken; Cheng, Ching Yu; Maillard, Pauline; van Heemst, Diana; Wong, Tien Yin; Niessen, Wiro J.; Beiser, Alexa S.; Beekman, Marian; Zhao, Wanting; Nyquist, Paul A.; Chen, Christopher; Launer, Lenore J.; Psaty, Bruce M.; Ikram, M. Kamran; Vernooij, Meike W.; Schmidt, Helena; Pausova, Zdenka; Becker, Diane M.; De Jager, Philip L.; Thompson, Paul M.; van Duijn, Cornelia M.; Bennett, David A.; Slagboom, P. Eline; Schmidt, Reinhold; Longstreth, W. T.; Ikram, M. Arfan; Seshadri, Sudha; Debette, Stéphanie; Gudnason, Vilmundur; Adams, Hieab H. H.; DeCarli, Charles (Springer Science and Business Media LLC, 2019-08-02)
    Brain lobar volumes are heritable but genetic studies are limited. We performed genome-wide association studies of frontal, occipital, parietal and temporal lobe volumes in 16,016 individuals, and replicated our findings in 8,789 individuals. We ...
  • Hollmann, Karsten; Allgaier, Katharina; Hohnecker, Carolin S.; Lautenbacher, Heinrich; Bizu, Verena; Nickola, Matthias; Wewetzer, Gunilla; Wewetzer, Christoph; Ivarsson, Tord; Skokauskas, Norbert; Wolters, Lidewij H.; Skarphéðinsson, Guðmundur Ágúst; Weidle, Bernhard; de Haan, Else; Torp, Nor Christan; Compton, Scott N.; Calvo, Rosa; Lera-Miguel, Sara; Haigis, Anna; Renner, Tobias J.; Conzelmann, Annette (2021-09)
    Cognitive behavioral therapy (CBT) is the first choice of treatment of obsessive–compulsive disorder (OCD) in children and adolescents. However, there is often a lack of access to appropriate treatment close to the home of the patients. An internet-based ...
  • van Mierlo, Pieter; Höller, Yvonne; Focke, Niels K.; Vulliemoz, Serge (2019)
    The evolution of EEG/MEG source connectivity is both, a promising, and controversial advance in the characterization of epileptic brain activity. In this narrative review we elucidate the potential of this technology to provide an intuitive view of the ...
  • Gerner, Nathalie; Thomschewski, Aljoscha; Marcu, Adrian; Trinka, Eugen; Höller, Yvonne (Frontiers Media SA, 2020-06-02)
    Aims: Intracranially recorded high-frequency oscillations (>80 Hz) are considered a candidate epilepsy biomarker. Recent studies claimed their detectability on the scalp surface. We aimed to investigate the applicability of high-frequency oscillation ...
  • Rodby-Bousquet, Elisabet; Ágústsson, Atli (2021-12-06)
    Purpose: To describe the use of assistive devices and postural asymmetries in lying, sitting and standing positions in adults with cerebral palsy, and to analyze postural asymmetries and any associations with their ability to maintain or change position ...
  • Stehle, Simon A.; Aubonnet, Romain; Hassan, Mahmoud; Recenti, Marco; Jacob, Deborah Cecelia Rose; Petersen, Hannes; Gargiulo, Paolo (2022-12-15)
    Introduction: Postural control is a sensorimotor mechanism that can reveal neurophysiological disorder. The present work studies the quantitative response to a complex postural control task. Methods: We measure electroencephalography (EEG), electromyography ...
  • On behalf of SLEEP REVOLUTION (2024-02)
    Sleep-disordered breathing, ranging from habitual snoring to severe obstructive sleep apnea, is a prevalent public health issue. Despite rising interest in sleep and awareness of sleep disorders, sleep research and diagnostic practices still rely on ...
  • Ng, R.; Björnsson, Hans Tómas; Fahrner, Jill A.; Harris, Jacqueline R. (2023-02)
    BACKGROUND: Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder caused by heterozygous variants in KMT2A. To date, the cognitive profile associated with WSS remains largely unknown, although emergent case series implicate increased risk of ...