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Ingrid E Scheffer

Showing results (1-10 of 585) with videos related to

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The Lancet. Neurology|November 2, 2015
PIK-ing the right gene for polymicrogyriaIngrid E Scheffer
Epilepsy Currents|December 4, 2015
Vaccination Triggers, Rather Than Causes, SeizuresIngrid E Scheffer
Epilepsia|March 1, 2023
The fascinating phenotypic spectrum of SCN1A gain-of-function epilepsiesIngrid E Scheffer
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 19, 2012
Diagnosis and long-term course of Dravet syndromeIngrid E Scheffer
The Lancet. Neurology|January 22, 2022
Lightning progress in child neurology in the past 20 yearsIngrid E Scheffer
Neurology|January 21, 2011
Does genotype determine phenotype? Sodium channel mutations in Dravet syndrome and GEFS+Ingrid E Scheffer
Epilepsy Currents|September 27, 2018
The Key to FAME: Intronic Repeat Expansions Cause Human EpilepsiesIngrid E Scheffer
Brain : a Journal of Neurology|February 5, 2003
Severe infantile epilepsies: molecular genetics challenge clinical classificationIngrid E Scheffer
Epilepsy Currents|August 13, 2011
Genetic testing in epilepsy: what should you be doing?Ingrid E Scheffer
Neurology|January 28, 2012
GLUT1 deficiency: a glut of epilepsy phenotypesIngrid E Scheffer
Pageof 59

Showing results (1-10 of 585) with videos related to

Sort By:
Pageof 59
The Lancet. Neurology|November 2, 2015
PIK-ing the right gene for polymicrogyriaIngrid E Scheffer
Epilepsy Currents|December 4, 2015
Vaccination Triggers, Rather Than Causes, SeizuresIngrid E Scheffer
Epilepsia|March 1, 2023
The fascinating phenotypic spectrum of SCN1A gain-of-function epilepsiesIngrid E Scheffer
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 19, 2012
Diagnosis and long-term course of Dravet syndromeIngrid E Scheffer
The Lancet. Neurology|January 22, 2022
Lightning progress in child neurology in the past 20 yearsIngrid E Scheffer
Neurology|January 21, 2011
Does genotype determine phenotype? Sodium channel mutations in Dravet syndrome and GEFS+Ingrid E Scheffer
Epilepsy Currents|September 27, 2018
The Key to FAME: Intronic Repeat Expansions Cause Human EpilepsiesIngrid E Scheffer
Brain : a Journal of Neurology|February 5, 2003
Severe infantile epilepsies: molecular genetics challenge clinical classificationIngrid E Scheffer
Epilepsy Currents|August 13, 2011
Genetic testing in epilepsy: what should you be doing?Ingrid E Scheffer
Neurology|January 28, 2012
GLUT1 deficiency: a glut of epilepsy phenotypesIngrid E Scheffer
Pageof 59