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Neuropharmacology
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May 16, 2020
Personalized medicine in genetic epilepsies - possibilities, challenges, and new frontiers
Ingo Helbig, Colin A Ellis
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 25, 2022
Base editing the synapse: Modeling a complex neurological disorder in non-human primates
Benjamin L Prosser, Ingo Helbig
Current Opinion in Neurology
|
February 23, 2013
Genetics of the epilepsies: where are we and where are we going?
Ingo Helbig, Daniel H Lowenstein
Annals of Neurology
|
May 10, 2018
Reply to "Recurrent SCN3A p.Ile875Thr variant in patients with polymicrogyria"
Ethan M Goldberg, Ingo Helbig
Molecular Syndromology
|
October 27, 2016
Understanding Genotypes and Phenotypes in Epileptic Encephalopathies
Ingo Helbig, Abou Ahmad N Tayoun
Epilepsy & Behavior : E&B
|
June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Current Opinion in Neurology
|
February 10, 2023
The current landscape of epilepsy genetics: where are we, and where are we going?
Sarah M Ruggiero, Julie Xian, Ingo Helbig
European Journal of Human Genetics : EJHG
|
September 27, 2012
Familial cosegregation of rare genetic variants with disease in complex disorders
Ingo Helbig, Susan E Hodge, Ruth Ottman
Epilepsy & Behavior : E&B
|
October 5, 2013
Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Epilepsy Currents
|
February 23, 2016
Attitudes Toward Epilepsy Genetics Testing Among Adult and Pediatric Epileptologists-Results of a Q-PULSE Survey
Lindsay Ferraro, John R Pollard, Ingo Helbig
Page
of 30
Search research articles
Search
Showing results (11-20 of 292) with videos related to
Sort By:
Page
of 30
Neuropharmacology
|
May 16, 2020
Personalized medicine in genetic epilepsies - possibilities, challenges, and new frontiers
Ingo Helbig, Colin A Ellis
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 25, 2022
Base editing the synapse: Modeling a complex neurological disorder in non-human primates
Benjamin L Prosser, Ingo Helbig
Current Opinion in Neurology
|
February 23, 2013
Genetics of the epilepsies: where are we and where are we going?
Ingo Helbig, Daniel H Lowenstein
Annals of Neurology
|
May 10, 2018
Reply to "Recurrent SCN3A p.Ile875Thr variant in patients with polymicrogyria"
Ethan M Goldberg, Ingo Helbig
Molecular Syndromology
|
October 27, 2016
Understanding Genotypes and Phenotypes in Epileptic Encephalopathies
Ingo Helbig, Abou Ahmad N Tayoun
Epilepsy & Behavior : E&B
|
June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Current Opinion in Neurology
|
February 10, 2023
The current landscape of epilepsy genetics: where are we, and where are we going?
Sarah M Ruggiero, Julie Xian, Ingo Helbig
European Journal of Human Genetics : EJHG
|
September 27, 2012
Familial cosegregation of rare genetic variants with disease in complex disorders
Ingo Helbig, Susan E Hodge, Ruth Ottman
Epilepsy & Behavior : E&B
|
October 5, 2013
Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Epilepsy Currents
|
February 23, 2016
Attitudes Toward Epilepsy Genetics Testing Among Adult and Pediatric Epileptologists-Results of a Q-PULSE Survey
Lindsay Ferraro, John R Pollard, Ingo Helbig
Page
of 30