Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

O K Steinlein

Showing results (1-10 of 45) with videos related to

Pageof 5
Sort By:
Revue Neurologique|September 3, 1999
Gene defects in idiopathic epilepsyO K Steinlein
Epilepsia|August 14, 1999
Idiopathic epilepsies with a monogenic mode of inheritanceO K Steinlein
Clinical Genetics|October 27, 1998
New insights into the molecular and genetic mechanisms underlying idiopathic epilepsiesO K Steinlein
European Journal of Pharmacology|April 20, 2000
Neuronal nicotinic receptors in human epilepsyO K Steinlein
American Journal of Medical Genetics|October 2, 2001
Genes and mutations in idiopathic epilepsyO K Steinlein
Der Nervenarzt|September 21, 2000
[Benign familial neonatal convulsions: molecular pathology and diagnosis]O K Steinlein
Human Genetics|May 14, 1999
Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsionsC Biervert, O K Steinlein
Biochemical Pharmacology|August 12, 2008
Neuronal nicotinic acetylcholine receptors: from the genetic analysis to neurological diseasesO K Steinlein, D Bertrand
European Journal of Pediatrics|August 7, 2007
Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean feverH Seidel, O K Steinlein
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 Steinlein
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Revue Neurologique|September 3, 1999
Gene defects in idiopathic epilepsyO K Steinlein
Epilepsia|August 14, 1999
Idiopathic epilepsies with a monogenic mode of inheritanceO K Steinlein
Clinical Genetics|October 27, 1998
New insights into the molecular and genetic mechanisms underlying idiopathic epilepsiesO K Steinlein
European Journal of Pharmacology|April 20, 2000
Neuronal nicotinic receptors in human epilepsyO K Steinlein
American Journal of Medical Genetics|October 2, 2001
Genes and mutations in idiopathic epilepsyO K Steinlein
Der Nervenarzt|September 21, 2000
[Benign familial neonatal convulsions: molecular pathology and diagnosis]O K Steinlein
Human Genetics|May 14, 1999
Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsionsC Biervert, O K Steinlein
Biochemical Pharmacology|August 12, 2008
Neuronal nicotinic acetylcholine receptors: from the genetic analysis to neurological diseasesO K Steinlein, D Bertrand
European Journal of Pediatrics|August 7, 2007
Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean feverH Seidel, O K Steinlein
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 Steinlein
Pageof 5