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Pflugers Archiv : European Journal of Physiology|December 18, 2009
Nicotinic receptor channelopathies and epilepsyOrtrud K Steinlein, Daniel BertrandEpilepsia|September 30, 2005
Asymmetry of long-latency auditory evoked potentials in LGI1-related autosomal dominant lateral temporal lobe epilepsyEylert Brodtkorb, Ortrud K Steinlein, Trond SandBMC Research Notes|March 19, 2013
Melanocortin-3-receptor promoter polymorphism associated with tuberculosis susceptibility does not influence protein expressionMarlene Eggert, Martina Pfob, Ortrud K SteinleinAnnals of Neurology|September 3, 2002
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizuresWenli Gu, Eylert Brodtkorb, Ortrud K SteinleinSeizure|August 11, 2012
The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsionsOrtrud K Steinlein, M Villain, C KorenkeNeuroscience Letters|July 3, 2007
A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikelyWenli Gu, Daniel Bertrand, Ortrud K SteinleinEpilepsy Research|December 4, 2003
No evidence for a seriously increased malignancy risk in LGI1-caused epilepsyEylert Brodtkorb, Karl O Nakken, Ortrud K SteinleinSeminars in Pediatric Neurology|July 26, 2002
Congenital myasthenic syndromesJoern P Sieb, Simone Kraner, Ortrud K SteinleinPageof 8