Cristin-person-ID: 16013
Person

Kaja Kristine Selmer

  • Stilling:
    Tilsatt
    ved Avdeling for medisinsk genetikk ved Oslo universitetssykehus HF
  • Stilling:
    Forsker
    ved Nasjonalt kompetansesenter for sjeldne epilepsirelaterte diagnoser (NK-SE) ved Oslo universitetssykehus HF

Resultater Resultater

A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome.

Fjær, Roar; Marciniak, Katarzyna; Sundnes, Olav; Hjorthaug, Hanne; Sheng, Ying; Hammarström, Clara; Sitek, Jan Cezary; Vigeland, Magnus Dehli; Backe, Paul Hoff; Øye, Ane-Marte mfl.. 2021, Human Molecular Genetics. TJHU, STOLAV, UIO, OUS, ANDREINSTVitenskapelig artikkel

Macrophage migration inhibitory factor: A potential biomarker for chronic low back pain in patients with Modic changes.

Gjefsen, Elisabeth; Gervin, Kristina; Goll, Guro Løvik; Bråten, Lars Christian Haugli; Wigemyr, Monica; Aass, Hans Christian D.; Vigeland, Maria Dehli; Schistad, Ellina Iordanova; Pedersen, Linda Margareth; Pripp, Are Hugo mfl.. 2021, RMD Open. DIAKONSYK, OSLOMET, UIO, OUSVitenskapelig artikkel

Climate change and epilepsy: Insights from clinical and basic science studies.

Gulcebi, Medine I.; Bartolini, Emanuele; Lee, Omay; Lisgaras, Christos Panagiotis; Onat, Filiz; Mifsud, Janet; Striano, Pasquale; Vezzani, Annamaria; Hildebrand, Michael S.; Jimenez-Jimenez, Diego mfl.. 2021, Epilepsy & Behavior. MONASH, UOMA, UNILU, UoG, UA, AECM, UNIVCAL, UoL, TRCoSiI, UL, USA, Lt, STORBRITAN, MELB, UMC, NYU, OUS, IRLAND, UCLH, SANGER, MÜ, ACU, RCH, NCL, UEF, UdSdF, UIO, MARIONEGRI, UdSdG, LUMC, USZ, UldB, ITALIA, MALTA, UCLVitenskapelig oversiktsartikkel/review

Trait impulsivity in Juvenile Myoclonic Epilepsy.

Shakeshaft, Amy; Panjwani, Naim; McDowall, Robert; Crudgington, Holly; Peña Ceballos, Javier; Andrade, Danielle M.; Beier, Christoph P.; Fong, Choong Yi; Gesche, Joanna; Greenberg, David A. mfl.. 2021, Annals of clinical and translational neurology. VV, USA, ESTLAND, CANADA, NEWC HOSP, OUH, CARDIFF, KU, SICKKIDS, GASLINI, OUS, UdSdP, SWANSEA, KCLUOL, UKVP, FNMOTOL, UM, NHS, UIO, UdSdG, MRCVitenskapelig artikkel

Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7.

Castilla-Vallmanya, Laura; Selmer, Kaja Kristine; Dimartino, Clémantine; Rabionet, Raquel; Blanco-Sanchez, Bernardo; Yang, Sandra; Reijnders, Margot R. F.; Essen, Antonie J. van; Oufadem, Myriam; Vigeland, Magnus Dehli mfl.. 2020, Genetics in Medicine. NU, UFdB, UOMA, HAUKELAND, VCU, UB, LILLE1, UoM, UBC, UM, UMCG, UDL, SLU, USA, SAND, CUitCoNY, UPS(I, OUS, FRANKRIKE, SUS, HCL, INSERM, UKHE, VICTORIA, UIO, FAU, CHARITE, ITALIAVitenskapelig artikkel
1 - 5 av 68 | Neste | Siste »