Mrs. Kate Esnault
Research Assistant
Medicine - Austin Health
21 Scholarly works
0 Projects
HIGHLIGHTS
2015
Journal article
Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy
DOI: 10.1016/j.eplepsyres.2015.09.0072015
Journal article
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
DOI: 10.1002/acn3.2242014
Journal article
Weight and fat distribution in patients taking valproate: A valproate-discordant gender-matched twin and sibling pair study
DOI: 10.1111/epi.127452014
Journal article
Genetics of epilepsy The testimony of twins in the molecular era
DOI: 10.1212/WNL.00000000000007902013
Journal article
Genetics of febrile seizure subtypes and syndromes: A twin study
DOI: 10.1016/j.eplepsyres.2013.02.0112013
Journal article
Autosomal dominant vasovagal syncope Clinical features and linkage to chromosome 15q26
DOI: 10.1212/WNL.0b013e31828cfad02012
Journal article
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency
DOI: 10.1111/epi.12007
RECENT SCHOLARLY WORKS
2012
Journal article
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies
DOI: 10.1002/ana.237022012
Journal article
Evidence for genetic factors in vasovagal syncope A twin-family study
DOI: 10.1212/WNL.0b013e31826357892012
Journal article
Familial Adult Myoclonic Epilepsy Recognition of Mild Phenotypes and Refinement of the 2q Locus
DOI: 10.1001/archneurol.2011.584