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Sarah E Heron

Showing results (1-10 of 42) with videos related to

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Journal of Medical Genetics|January 25, 2013
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropySarah E Heron, Leanne M Dibbens
Epilepsia|March 15, 2011
Proposed genetic classification of the "benign" familial neonatal and infantile epilepsiesJohn C Mulley, Sarah E Heron, Leanne M Dibbens
American Journal of Medical Genetics. Part A|August 3, 2016
BRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblingsNicholas J Smith, Jill Lipsett, Leanne M Dibbens, et al.
Journal of Medical Genetics|January 8, 2016
KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effectsChiao Xin Lim, Michael G Ricos, Leanne M Dibbens, et al.
Epilepsia|September 9, 2011
"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!John C Mulley, Sarah E Heron, Robyn H Wallace, et al.
Epilepsy Research|April 17, 2007
Association studies and functional validation or functional validation alone?Sarah E Heron, Louisa Sanchez, Ingrid E Scheffer, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Channelopathies in idiopathic epilepsySarah E Heron, Ingrid E Scheffer, Samuel F Berkovic, et al.
Epilepsia|April 29, 2005
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?Nigel C K Tan, Sarah E Heron, Ingrid E Scheffer, et al.
Neurology Research International|July 26, 2011
The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile SeizuresJohn C Mulley, Xenia Iona, Bree Hodgson, et al.
Epilepsia|March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|January 25, 2013
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropySarah E Heron, Leanne M Dibbens
Epilepsia|March 15, 2011
Proposed genetic classification of the "benign" familial neonatal and infantile epilepsiesJohn C Mulley, Sarah E Heron, Leanne M Dibbens
American Journal of Medical Genetics. Part A|August 3, 2016
BRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblingsNicholas J Smith, Jill Lipsett, Leanne M Dibbens, et al.
Journal of Medical Genetics|January 8, 2016
KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effectsChiao Xin Lim, Michael G Ricos, Leanne M Dibbens, et al.
Epilepsia|September 9, 2011
"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!John C Mulley, Sarah E Heron, Robyn H Wallace, et al.
Epilepsy Research|April 17, 2007
Association studies and functional validation or functional validation alone?Sarah E Heron, Louisa Sanchez, Ingrid E Scheffer, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Channelopathies in idiopathic epilepsySarah E Heron, Ingrid E Scheffer, Samuel F Berkovic, et al.
Epilepsia|April 29, 2005
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?Nigel C K Tan, Sarah E Heron, Ingrid E Scheffer, et al.
Neurology Research International|July 26, 2011
The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile SeizuresJohn C Mulley, Xenia Iona, Bree Hodgson, et al.
Epilepsia|March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Pageof 5