Bowhead NEIL1: molecular cloning, characterization, and enzymatic properties von Holm, Signe, Larsen, Rikke Møller, Holst, Camilla Myrup, Heide-Jørgensen, Mads Peter, Steffensen, John Fleng, Stevnsner, Tinna, Larsen, Knud

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Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy von Møller, Rikke S, Weckhuysen, Sarah, Chipaux, Mathilde, Marsan, Elise, Taly, Valerie, Bebin, E Martina, Hiatt, Susan M, Prokop, Jeremy W, Bowling, Kevin M, Mei, Davide, Conti, Valerio, de la Grange, Pierre, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Lambrecq, Virginie, Larsen, Line H G, Leguern, Eric, Guerrini, Renzo, Rubboli, Guido, Cooper, Gregory M, Baulac, Stéphanie

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Erratum: Sequence analysis of 17 NRXN1 deletions von Hoeffding, Louise K., Hansen, Thomas, Ingason, Andrés, Doung, Linh, Thygesen, Johan H., Møller, Rikke S., Tommerup, Niels, Kirov, George, Rujescu, Dan, Larsen, Lars A., Werge, Thomas

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Utility of genetic testing for therapeutic decision‐making in adults with epilepsy von Johannesen, Katrine M., Nikanorova, Natalya, Marjanovic, Dragan, Pavbro, Agnieszka, Larsen, Line H. G., Rubboli, Guido, Møller, Rikke S.

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Sequence analysis of 17 NRXN1 deletions von Hoeffding, Louise Kristine Enggaard, Hansen, Thomas, Ingason, Andrés, Doung, Linh, Thygesen, Johan H., Møller, Rikke S., Tommerup, Niels, Kirov, George, Rujescu, Dan, Larsen, Lars A., Werge, Thomas

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Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation von Gardella, Elena, Becker, Felicitas, Møller, Rikke S., Schubert, Julian, Lemke, Johannes R., Larsen, Line H. G., Eiberg, Hans, Nothnagel, Michael, Thiele, Holger, Altmüller, Janine, Syrbe, Steffen, Merkenschlager, Andreas, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Mang, Yuan, Bakke Møller, Louise, Gellert, Pia, Heron, Sarah E., Dibbens, Leanne M., Weckhuysen, Sarah, Dahl, Hans Atli, Biskup, Saskia, Tommerup, Niels, Hjalgrim, Helle, Lerche, Holger, Beniczky, Sándor, Weber, Yvonne G.

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Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies von Johannesen, Katrine, Marini, Carla, Pfeffer, Siona, Møller, Rikke S, Dorn, Thomas, Niturad, Christina, Gardella, Elena, Weber, Yvonne, Søndergård, Marianne, Hjalgrim, Helle, Nikanorova, Mariana, Becker, Felicitas, Larsen, Line H.G, Dahl, Hans A, Maier, Oliver, Mei, Davide, Biskup, Saskia, Klein, Karl M, Reif, Philipp S, Rosenow, Felix, Elias, Abdallah F, Hudson, Cindy, Helbig, Katherine L, Schubert-Bast, Susanne, Scordo, Maria R, Craiu, Dana, Djémié, Tania, Hoffman-Zacharska, Dorota, Caglayan, Hande, Helbig, Ingo, Serratosa, Jose, Striano, Pasquale, De Jonghe, Peter, Weckhuysen, Sarah, Suls, Arvid, Muru, Kai, Talvik, Inga, Talvik, Tiina, Muhle, Hiltrud, Borggraefe, Ingo, Rost, Imma, Guerrini, Renzo, Lerche, Holger, Lemke, Johannes R, Rubboli, Guido, Maljevic, Snezana

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Parental mosaicism in epilepsies due to alleged de novo variants von Møller, Rikke S., Liebmann, Nora, Larsen, Line H. G., Stiller, Mathias, Hentschel, Julia, Kako, Nahrain, Abdin, Dalia, Di Donato, Nataliya, Pal, Deb K., Zacher, Pia, Syrbe, Steffen, Dahl, Hans A., Lemke, Johannes R.

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Mutations in GABRB3: From febrile seizures to epileptic encephalopathies von Møller, Rikke S, Wuttke, Thomas V, Helbig, Ingo, Marini, Carla, Johannesen, Katrine M, Brilstra, Eva H, Vaher, Ulvi, Borggraefe, Ingo, Talvik, Inga, Talvik, Tiina, Kluger, Gerhard, Francois, Laurence L, Lesca, Gaetan, de Bellescize, Julitta, Blichfeldt, Susanne, Chatron, Nicolas, Holert, Nils, Jacobs, Julia, Swinkels, Marielle, Betzler, Cornelia, Syrbe, Steffen, Nikanorova, Marina, Myers, Candace T, Larsen, Line H.G, Vejzovic, Sabina, Pendziwiat, Manuela, von Spiczak, Sarah, Hopkins, Sarah, Dubbs, Holly, Mang, Yuan, Mukhin, Konstantin, Holthausen, Hans, van Gassen, Koen L, Dahl, Hans A, Tommerup, Niels, Mefford, Heather C, Rubboli, Guido, Guerrini, Renzo, Lemke, Johannes R, Lerche, Holger, Muhle, Hiltrud, Maljevic, Snezana

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Diagnostic Yield of Genetic Testing in Young Patients With Atrioventricular Block of Unknown Cause von Resdal Dyssekilde, Johnni, Frederiksen, Tanja Charlotte, Christiansen, Morten Krogh, Hasle Sørensen, Rikke, Pedersen, Lisbeth Nørum, Loof Møller, Peter, Christensen, Lene Svendstrup, Larsen, Jacob Moesgaard, Thomsen, Kristian Korsgaard, Lindhardt, Tommi Bo, Böttcher, Morten, Molsted, Stig, Havndrup, Ole, Fischer, Thomas, Møller, Dorthe Svenstrup, Henriksen, Finn Lund, Johansen, Jens Brock, Nielsen, Jens Cosedis, Bundgaard, Henning, Nygaard, Mette, Jensen, Henrik Kjærulf

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PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics von Bayat, Allan, Knaus, Alexej, Juul, Annika Wollenberg, Dukic, Dejan, Gardella, Elena, Charzewska, Agnieszka, Clement, Emma, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Horn, Denise, Horton, Rachel, Hurst, Jane A., Josifova, Dragana, Larsen, Line H. G., Lascelles, Karine, Obersztyn, Ewa, Pagnamenta, Alistair, Pal, Deb K., Pendziwiat, Manuela, Ryten, Mina, Taylor, Jenny, Vogt, Julie, Weber, Yvonne, Krawitz, Peter M., Helbig, Ingo, Kini, Usha, Møller, Rikke S.

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome von Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

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Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies von Møller, Rikke S., Larsen, Line H.G., Johannesen, Katrine M., Talvik, Inga, Talvik, Tiina, Vaher, Ulvi, Miranda, Maria J., Farooq, Muhammad, Nielsen, Jens E.K., Lavard Svendsen, Lene, Kjelgaard, Ditte B., Linnet, Karen M., Hao, Qin, Uldall, Peter, Frangu, Mimoza, Tommerup, Niels, Baig, Shahid M., Abdullah, Uzma, Born, Alfred P., Gellert, Pia, Nikanorova, Marina, Olofsson, Kern, Jepsen, Birgit, Marjanovic, Dragan, Al-Zehhawi, Lana I.K., Peñalva, Sofia J., Krag-Olsen, Bente, Brusgaard, Klaus, Hjalgrim, Helle, Rubboli, Guido, Pal, Deb K., Dahl, Hans A.

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Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia von Larsen, Rikke Hebo, Utke Rank, Cecilie, Grell, Kathrine, Nørgaard Møller, Lisbeth, Malthe Overgaard, Ulrik, Kampmann, Peter, Nersting, Jacob, Degn, Matilda, Nygaard Nielsen, Stine, Holst, Helle, Klug Albertsen, Birgitte, Skov Wehner, Peder, Thude Callesen, Michael, Kanerva, Jukka, Leth Frandsen, Thomas, Als-Nielsen, Bodil, Lyngsie Hjalgrim, Lisa, Schmiegelow, Kjeld

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Incorporating epilepsy genetics into clinical practice: a 360°evaluation von Oates, Stephanie, Tang, Shan, Rosch, Richard, Lear, Rosalie, Hughes, Elaine F., Williams, Ruth E., Larsen, Line H. G., Hao, Qin, Dahl, Hans Atli, Møller, Rikke S., Pal, Deb K.

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Automatic continuous EEG signal analysis for diagnosis of delirium in patients with sepsis von Urdanibia-Centelles, Olalla, Nielsen, Rikke M., Rostrup, Egill, Vedel-Larsen, Esben, Thomsen, Kirsten, Nikolic, Miki, Johnsen, Birger, Møller, Kirsten, Lauritzen, Martin, Benedek, Krisztina

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Clinical Staphylococcus aureus inhibits human T-cell activity through interaction with the PD-1 receptor von Mellergaard, Maiken, Skovbakke, Sarah Line, Jepsen, Stine Dam, Panagiotopoulou, Nafsika, Hansen, Amalie Bøge Rud, Tian, Weihua, Lund, Astrid, Høgh, Rikke Illum, Møller, Sofie Hedlund, Guérillot, Romain, Hayes, Ashleigh S, Erikstrup, Lise Tornvig, Andresen, Lars, Peleg, Anton Y, Larsen, Anders Rhod, Stinear, Timothy P, Handberg, Aase, Erikstrup, Christian, Howden, Benjamin P, Goletz, Steffen, Frees, Dorte, Skov, Søren

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Phenotypic and genetic spectrum of SCN8A‐related disorders, treatment options, and outcomes von Gardella, Elena, Møller, Rikke S.

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Mutations in KCNT1 cause a spectrum of focal epilepsies von Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., Kempen, Marjan J. A., Klinkenberg, Sylvia, Andrews, Ian, Kelley, Kent, Ronen, Gabriel M., Callen, David, McMahon, Jacinta M., Yendle, Simone C., Carvill, Gemma L., Mefford, Heather C., Nabbout, Rima, Poduri, Annapurna, Striano, Pasquale, Baglietto, Maria G., Zara, Federico, Smith, Nicholas J., Pridmore, Clair, Gardella, Elena, Nikanorova, Marina, Dahl, Hans Atli, Gellert, Pia, Scheffer, Ingrid E., Gunning, Boudewijn, Kragh‐Olsen, Bente, Dibbens, Leanne M.

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Exercise in newly diagnosed patients with multiple myeloma: A randomized controlled trial of effects on physical function, physical activity, lean body mass, bone mineral density,... von Larsen, Rikke F., Jarden, Mary, Minet, Lisbeth R., Frølund, Ulf Christian, Hermann, Anne Pernille, Breum, Leif, Möller, Sören, Abildgaard, Niels

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