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Expert Review of Neurotherapeutics|November 25, 2010
Animal models for autosomal dominant frontal lobe epilepsy: on the origin of seizuresOrtrud K SteinleinEuropean Journal of Pain (London, England)|March 13, 2002
Channelopathies can cause epilepsy in manOrtrud K SteinleinEpilepsia|June 26, 2003
A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsyTobias Leniger, Colette Kananura, Andreas Hufnagel, et al.Neurobiology of Disease|June 21, 2005
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficitsDaniel Bertrand, Frances Elmslie, Elaine Hughes, et al.Epilepsia|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 SteinleinPageof 19