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Epilepsia
|
April 21, 2018
Commentary: The genetic architecture of the epilepsies, as told by 8500 gene panels
Ingo Helbig
Seminars in Neurology
|
June 11, 2015
Genetic Causes of Generalized Epilepsies
Ingo Helbig
Progress in Brain Research
|
September 8, 2014
New technologies in molecular genetics: the impact on epilepsy research
Ingo Helbig
Plos Genetics
|
January 7, 2021
The dose makes the poison-Novel insights into Dravet syndrome and SCN1A regulation through nonproductive splicing
Ingo Helbig, Ethan Goldberg
Neurology
|
January 31, 2018
Teaching NeuroImages: Atrophy in epileptic encephalopathy
Ingo Helbig, Laura Adang
Neurology
|
June 2, 2017
Advancing the phenome alongside the genome in epilepsy studies
Ingo Helbig, Dick Lindhout
Epilepsia
|
February 4, 2015
Commentary: Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry
Deb Pal, Ingo Helbig
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 31, 2023
Guardians of the epilepsy genome
Julie Xian, Ingo Helbig
Annals of Neurology
|
December 7, 2024
NORSE, FIRES, and a Polygenic Trickle of Autoimmunity
Ingo Helbig, Shiva Ganesan
Neurology
|
July 28, 2017
Epileptic encephalopathy, movement disorder, and the yin and yang of <i>GNAO1</i> function
Toni S Pearson, Ingo Helbig
Page
of 30
Search research articles
Search
Showing results (1-10 of 292) with videos related to
Sort By:
Page
of 30
Epilepsia
|
April 21, 2018
Commentary: The genetic architecture of the epilepsies, as told by 8500 gene panels
Ingo Helbig
Seminars in Neurology
|
June 11, 2015
Genetic Causes of Generalized Epilepsies
Ingo Helbig
Progress in Brain Research
|
September 8, 2014
New technologies in molecular genetics: the impact on epilepsy research
Ingo Helbig
Plos Genetics
|
January 7, 2021
The dose makes the poison-Novel insights into Dravet syndrome and SCN1A regulation through nonproductive splicing
Ingo Helbig, Ethan Goldberg
Neurology
|
January 31, 2018
Teaching NeuroImages: Atrophy in epileptic encephalopathy
Ingo Helbig, Laura Adang
Neurology
|
June 2, 2017
Advancing the phenome alongside the genome in epilepsy studies
Ingo Helbig, Dick Lindhout
Epilepsia
|
February 4, 2015
Commentary: Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry
Deb Pal, Ingo Helbig
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 31, 2023
Guardians of the epilepsy genome
Julie Xian, Ingo Helbig
Annals of Neurology
|
December 7, 2024
NORSE, FIRES, and a Polygenic Trickle of Autoimmunity
Ingo Helbig, Shiva Ganesan
Neurology
|
July 28, 2017
Epileptic encephalopathy, movement disorder, and the yin and yang of <i>GNAO1</i> function
Toni S Pearson, Ingo Helbig
Page
of 30