Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
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.
Published in Annals of neurology (01.03.2016)
Published in Annals of neurology (01.03.2016)
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Mutations in KCNT1 cause a spectrum of focal epilepsies
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.
Published in Epilepsia (Copenhagen) (01.09.2015)
Published in Epilepsia (Copenhagen) (01.09.2015)
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Identification of male heterogametic sex‐determining regions on the Atlantic herring Clupea harengus genome
í Kongsstovu, Sunnvør, Dahl, Hans Atli, Gislason, Hannes, Homrum, Eydna, Jacobsen, Jan Arge, Flicek, Paul, Mikalsen, Svein‐Ole
Published in Journal of fish biology (01.07.2020)
Published in Journal of fish biology (01.07.2020)
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Incorporating epilepsy genetics into clinical practice: a 360°evaluation
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
Published in Npj genomic medicine (10.05.2018)
Published in Npj genomic medicine (10.05.2018)
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The role of SLC2A1 in early onset and childhood absence epilepsies
Muhle, Hiltrud, Helbig, Ingo, Frøslev, Tobias Guldberg, Suls, Arvid, von Spiczak, Sarah, Klitten, Laura Line, Dahl, Hans Atli, Brusgaard, Klaus, Neubauer, Bernd, De Jonghe, Peter, Tommerup, Niels, Stephani, Ulrich, Hjalgrim, Helle, Møller, Rikke Steensbjerre
Published in Epilepsy research (01.07.2013)
Published in Epilepsy research (01.07.2013)
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D-galactose Supplementation for the Treatment of Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE): A Pilot Trial of Precision Medicine After Epilepsy Surgery
Aledo-Serrano, Ángel, Valls-Carbó, Adrián, Fenger, Christina D., Groeppel, Gudrun, Hartlieb, Till, Pascual, Irene, Herraez, Erika, Cabal, Borja, García-Morales, Irene, Toledano, Rafael, Budke, Marcelo, Beltran-Corbellini, Álvaro, Baldassari, Sara, Coras, Roland, Kobow, Katja, Herrera, David M., del Barrio, Antonio, Dahl, Hans Atli, del Pino, Isabel, Baulac, Stéphanie, Blumcke, Ingmar, Møller, Rikke S., Gil-Nagel, Antonio
Published in Neurotherapeutics (01.09.2023)
Published in Neurotherapeutics (01.09.2023)
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Atlantic herring (Clupea harengus) population structure in the Northeast Atlantic Ocean
í Kongsstovu, Sunnvør, Mikalsen, Svein-Ole, Homrum, Eydna í, Jacobsen, Jan Arge, Als, Thomas D., Gislason, Hannes, Flicek, Paul, Nielsen, Einar Eg, Dahl, Hans Atli
Published in Fisheries research (01.05.2022)
Published in Fisheries research (01.05.2022)
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Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution
Frasca, Angelisa, Pavlidou, Efterpi, Bizzotto, Matteo, Gao, Yunan, Balestra, Dario, Pinotti, Mirko, Dahl, Hans Atli, Mazarakis, Nicholas D, Landsberger, Nicoletta, Kinali, Maria
Published in Neurology. Genetics (01.04.2022)
Published in Neurology. Genetics (01.04.2022)
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Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies
Tiefes, Anna M, Hartlieb, Till, Tacke, Moritz, von Stülpnagel-Steinbeis, Celina, Larsen, Line H G, Hao, Quin, Dahl, Hans Atli, Neubauer, Bernd A, Gerstl, Lucia, Kudernatsch, Manfred, Kluger, Gerhard J, Borggraefe, Ingo
Published in Clinical EEG and neuroscience (01.07.2019)
Published in Clinical EEG and neuroscience (01.07.2019)
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Gardella, Elena, Beniczky, Sándor, Møller, Rikke S., Becker, Felicitas, Lemke, Johannes R., Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E., Dibbens, Leanne M., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G.
Published in Annals of neurology (01.07.2016)
Published in Annals of neurology (01.07.2016)
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Gardella, Elena, Beniczky, Sándor, Møller, Rikke S., Becker, Felicitas, Lemke, Johannes R., Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E., Dibbens, Leanne M., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G.
Published in Annals of neurology (01.07.2016)
Published in Annals of neurology (01.07.2016)
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Gardella, Elena, Beniczky, Sándor, Møller, Rikke S., Becker, Felicitas, Lemke, Johannes R., Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E., Dibbens, Leanne M., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G.
Published in Annals of neurology (01.07.2016)
Published in Annals of neurology (01.07.2016)
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Gardella, Elena, Beniczky, Sándor, Moller, Rikke S, Becker, Felicitas, Lemke, Johannes R, Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nurnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E, Dibbens, Leanne M, Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G
Published in Annals of neurology (01.07.2016)
Published in Annals of neurology (01.07.2016)
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A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene
GREGERSEN, Noomi, DAHL, Hans A, KRISTENSEN, Ann S, KRUSE, Torben A, BØRGLUM, Anders D, MORS, Ole, BUTTENSCHØN, Henriette N, NYEGAARD, Mette, HEDEMAND, Anne, ALS, Thomas D, WANG, August G, JOENSEN, Sofus, WOLDBYE, David Pd, KOEFOED, Pernille
Published in European journal of human genetics : EJHG (01.01.2012)
Published in European journal of human genetics : EJHG (01.01.2012)
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Mutations in KCNT 1 cause a spectrum of focal epilepsies
Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., van 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.
Published in Epilepsia (Copenhagen) (01.09.2015)
Published in Epilepsia (Copenhagen) (01.09.2015)
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Gardella, Elena, Beniczky, Sándor, Møller, Rikke S, Becker, Felicitas, Lemke, Johannes R, Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E, Dibbens, Leanne M, Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G
Published in Annals of neurology (01.07.2016)
Published in Annals of neurology (01.07.2016)
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Gardella, Elena, Beniczky, Sándor, Møller, Rikke S, Becker, Felicitas, Lemke, Johannes R, Syrbe, Steffen, Eiberg, Hans, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Gellert, Pia, Dahl, Hans Atli, Weckhuysen, Sarah, Heron, Sarah E, Dibbens, Leanne M, Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne G
Published in Annals of neurology (01.07.2016)
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Published in Annals of neurology (01.07.2016)
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