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Human Genetics|May 14, 1999
Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsionsC Biervert, O K SteinleinNeuroscience Letters|November 17, 2001
Semiquantitative expression analysis of ephrine-receptor tyrosine kinase mRNA's in a rat model of traumatic brain injuryC Biervert, E Horvath, T FahrigNeuroreport|June 11, 1999
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsyO K Steinlein, J Stoodt, C Biervert, et al.Neuroreport|July 7, 2000
The new voltage gated potassium channel KCNQ5 and neonatal convulsionsC Kananura, C Biervert, M Hechenberger, et al.Neuropediatrics|April 25, 2000
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish familyW L Lee, C Biervert, K Hallmann, et al.Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.Annals of Neurology|September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsH Lerche, C Biervert, A K Alekov, et al.Pageof 1