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Author/Creator Gellert, Pia

1. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. Issue 3 (13th February 2016)

Authors:
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 Mølle...
Journal:
Annals of neurology
Issue:
Volume 79:Issue 3(2016:Mar.)
Page Start:
428
Record Type:
Journal Article
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2. Mutations in KCNT1 cause a spectrum of focal epilepsies. (30th June 2015)

Authors:
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.; N...
Journal:
Epilepsia
Issue:
Volume 56:issue 9(2015:Sep.)
Page Start:
e114
Record Type:
Journal Article
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3. Reply. Issue 1 (10th May 2016)

Authors:
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; Web...
Journal:
Annals of neurology
Issue:
Volume 80:Issue 1(2016:Jul.)
Page Start:
168
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗