A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome von Fjær, Roar, Marciniak, Katarzyna, Sundnes, Olav, Hjorthaug, Hanne, Sheng, Ying, Hammarström, Clara, Sitek, Jan Cezary, Vigeland, Magnus Dehli, Backe, Paul Hoff, Øye, Ane-Marte, Fosse, Johanna Hol, Stav-Noraas, Tor Espen, Uchiyama, Yuri, Matsumoto, Naomichi, Comi, Anne, Pevsner, Jonathan, Haraldsen, Guttorm, Selmer, Kaja Kristine

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Combined inhibition of the cell cycle related proteins Wee1 and Chk1/2 induces synergistic anti-cancer effect in melanoma von Magnussen, Gry Irene, Emilsen, Elisabeth, Giller Fleten, Karianne, Engesæter, Birgit, Nähse-Kumpf, Viola, Fjær, Roar, Slipicevic, Ana, Flørenes, Vivi Ann

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Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorder von Bjørgo, Kathrine, Fjær, Roar, Mørk, Hanne Håberg, Ferdinandusse, Sacha, Falkenberg, Kim D., Waterham, Hans R., Øye, Ane-Marte, Sikiric, Alma, Amundsen, Silja Svanstrøm, Kulseth, Mari Ann, Selmer, Kaja

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Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport von Moen, Marivi Nabong, Fjær, Roar, Hamdani, El Hassan, Laerdahl, Jon K, Menchini, Robin Johansen, Vigeland, Magnus Dehli, Sheng, Ying, Undlien, Dag Erik, Hassel, Bjørnar, Salih, Mustafa A, El Khashab, Heba Y, Selmer, Kaja Kristine, Chaudhry, Farrukh Abbas

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STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy von Stamberger, Hannah, Nikanorova, Marina, Willemsen, Marjolein H, Accorsi, Patrizia, Angriman, Marco, Baier, Hartmut, Benkel-Herrenbrueck, Ira, Benoit, Valérie, Budetta, Mauro, Caliebe, Almuth, Cantalupo, Gaetano, Capovilla, Giuseppe, Casara, Gianluca, Courage, Carolina, Deprez, Marie, Destrée, Anne, Dilena, Robertino, Erasmus, Corrie E, Fannemel, Madeleine, Fjær, Roar, Giordano, Lucio, Helbig, Katherine L, Heyne, Henrike O, Klepper, Joerg, Kluger, Gerhard J, Lederer, Damien, Lodi, Monica, Maier, Oliver, Merkenschlager, Andreas, Michelberger, Nina, Minetti, Carlo, Muhle, Hiltrud, Phalin, Judith, Ramsey, Keri, Romeo, Antonino, Schallner, Jens, Schanze, Ina, Shinawi, Marwan, Sleegers, Kristel, Sterbova, Katalin, Syrbe, Steffen, Traverso, Monica, Tzschach, Andreas, Uldall, Peter, Van Coster, Rudy, Verhelst, Helene, Viri, Maurizio, Winter, Susan, Wolff, Markus, Zenker, Martin, Zoccante, Leonardo, De Jonghe, Peter, Helbig, Ingo, Striano, Pasquale, Lemke, Johannes R, Møller, Rikke S, Weckhuysen, Sarah

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Exome sequencing in monogenic epilepsies. Genetic and functional studies of monogenic constitutional and somatic epilepsies von Fjær, Roar

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Vi foreslår "anfallsforebyggende epilepsimedisin" von Myren-Svelstad, Sverre, Fjær, Roar

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We suggest ‘antiseizure epileptic drug’ von Myren-Svelstad, Sverre, Fjær, Roar

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Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2 von Fjaer, Roar, Brodtkorb, Eylert, Øye, Ane-Marte, Sheng, Ying, Vigeland, Magnus Dehli, Kvistad, Kjell Arne, Backe, Paul Hoff, Selmer, Kaja Kristine

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A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome von Fjær, Roar, Marciniak, Katarzyna, Sundnes, Olav, Hjorthaug, Hanne, Sheng, Ying, Hammarström, Clara Louise, Sitek, Jan Cezary, Vigeland, Magnus Dehli, Backe, Paul Hoff, Øye, Ane-Marte, Hol, Johanna, Stav-Noraas, Tor Espen, Uchiyama, Yuri, Matsumoto, Naomichi, Comi, Anne, Pevsner, Jonathan, Haraldsen, Guttorm, Selmer, Kaja Kristine

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Agder Living Lab - Følgeforskningsrapport von Eikebrokk, Tom Roar, Helmersen, Migle, Lindland, Kristiane Marie Fjær

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Agder Living Lab - Følgeforskningsrapport von Eikebrokk, Tom Roar, Helmersen, Migle, Lindland, Kristiane Marie Fjær

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Agder Living Lab - Følgeforskningsrapport von Eikebrokk, Tom Roar, Helmersen, Migle, Lindland, Kristiane Marie Fjær

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Discrete-Time Backstepping Design Applied to Position Tracking Control of an Electro-Pneumatic Clutch Actuator von Isaksen Trond Willi , Norges teknisk-naturvitenskapelige universitet, Institutt for teknisk kybernetikk

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