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L M Dibbens

Showing results (1-10 of 8) with videos related to

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Genes, Brain, and Behavior|June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex geneticsL M Dibbens, S E Heron, J C Mulley
The Pharmacogenomics Journal|December 18, 2013
SCN1A variations and response to multiple antiepileptic drugsT S C Yip, C O'Doherty, N C K Tan, et al.
Neuroscience Letters|May 12, 2009
The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsiesL M Dibbens, L A Harkin, M Richards, et al.
Neurology|April 27, 2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutationsL M Dibbens, R Kneen, M A Bayly, et al.
Genes, Brain, and Behavior|March 3, 2007
NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivityL M Dibbens, J Ekberg, I Taylor, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Annals of Neurology|October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failureL M Dibbens, R Michelucci, A Gambardella, et al.
Neurology|July 15, 2011
De novo SCN1A mutations in migrating partial seizures of infancyD Carranza Rojo, L Hamiwka, J M McMahon, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genes, Brain, and Behavior|June 15, 2007
A polygenic heterogeneity model for common epilepsies with complex geneticsL M Dibbens, S E Heron, J C Mulley
The Pharmacogenomics Journal|December 18, 2013
SCN1A variations and response to multiple antiepileptic drugsT S C Yip, C O'Doherty, N C K Tan, et al.
Neuroscience Letters|May 12, 2009
The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsiesL M Dibbens, L A Harkin, M Richards, et al.
Neurology|April 27, 2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutationsL M Dibbens, R Kneen, M A Bayly, et al.
Genes, Brain, and Behavior|March 3, 2007
NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivityL M Dibbens, J Ekberg, I Taylor, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Annals of Neurology|October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failureL M Dibbens, R Michelucci, A Gambardella, et al.
Neurology|July 15, 2011
De novo SCN1A mutations in migrating partial seizures of infancyD Carranza Rojo, L Hamiwka, J M McMahon, et al.
Pageof 1