Simone C. Yendle
Heidelberg, VIC, Australia
Last Updated: 09/26/2026
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Found 8 publications
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
Journal: Epilepsia
Published: April 03, 2015
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.
Journal: Epilepsia
Published: March 04, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.
Journal: Epilepsia
Published: January 17, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Journal: Nature genetics
Published: December 28, 2012
GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
Journal: Nature genetics
Published: November 20, 2012
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Journal: Annals of neurology
Published: January 26, 2012
Rare copy number variants are an important cause of epileptic encephalopathies.
Journal: Annals of neurology
Published: December 23, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026