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BMC Medical Genetics|March 18, 2018
Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case reportE C Sattler, O K SteinleinCurrent Opinion in Genetics & Development|May 29, 2000
Ion channels and epilepsy in man and mouseO K Steinlein, J L NoebelsEpilepsia|January 30, 1999
Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected membersK O Nakken, A Magnusson, O K SteinleinTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 7, 1998
[Autosomal dominant nocturnal frontal lobe epilepsy. An electroclinical and genetic description of a Norwegian family with ten affected members]K O Nakken, A Magnusson, O K SteinleinAmerican Journal of Medical Genetics|February 25, 2000
Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsyK Hallmann, M Durner, T Sander, et al.Epilepsia|September 16, 1999
Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepineF Picard, S Bertrand, O K Steinlein, et al.Human Genetics|October 13, 2000
Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by epsilon-AChR subunit truncating mutationsJ P Sieb, S Kraner, M Rauch, et al.Neuroreport|December 1, 2001
Cloning and mutation analysis of the human potassium channel KCNQ2 gene promoterJ F Xiao, C Fischer, O K Steinlein, et al.Neuroreport|June 11, 1999
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsyO K Steinlein, J Stoodt, C Biervert, et al.Neurogenetics|April 14, 2005
LGI1: a gene involved in epileptogenesis and glioma progression?W Gu, E Brodtkorb, T Piepoli, et al.Pageof 40