Hadassa Goldberg‐Stern

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Sarah E. Heron, Bronwyn E. Grinton, Sara Kivity et al. · The American Journal of Human Genetics · 2012 · 258 citations · Full text

Developmental Anomaly, Genetic Disorder, Choreoathetosis Syndrome +6

Clinical spectrum and medical treatment of children with electrical status epilepticus in sleep (ESES)

Uri Kramer, Liora Sagi, Hadassa Goldberg‐Stern et al. · Epilepsia · 2008 · 194 citations · Full text

Early onset epileptic encephalopathy caused by de novo <i><scp>SCN</scp>8A</i> mutations

Chihiro Ohba, Mitsuhiro Kato, Satoru Takahashi et al. · Epilepsia · 2014 · 169 citations

Genotype–phenotype analysis of human frontoparietal polymicrogyria syndromes

Xianhua Piao, Bernard S. Chang, Adria Bodell et al. · Annals of Neurology · 2005 · 151 citations · Full text

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

Todor Arsov, Saul A. Mullen, Sue Rogers et al. · Annals of Neurology · 2012 · 142 citations