H
Hadassa Goldberg-Stern
Researcher at Tel Aviv University
Publications - 57
Citations - 2303
Hadassa Goldberg-Stern is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Epilepsy & Generalized epilepsy. The author has an hindex of 23, co-authored 55 publications receiving 1999 citations. Previous affiliations of Hadassa Goldberg-Stern include University of Cincinnati & Children's Medical Center of Dallas.
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Journal ArticleDOI
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Sarah E. Heron,Bronwyn E. Grinton,Sara Kivity,Zaid Afawi,Sameer M. Zuberi,James N. Hughes,Clair Pridmore,Bree L. Hodgson,Xenia Iona,Lynette G. Sadleir,James T. Pelekanos,James T. Pelekanos,Eric Herlenius,Hadassa Goldberg-Stern,Haim Bassan,Eric Haan,Amos D. Korczyn,Alison Gardner,Mark A. Corbett,Jozef Gecz,Jozef Gecz,Paul Q. Thomas,John C. Mulley,John C. Mulley,Samuel F. Berkovic,Ingrid E. Scheffer,Ingrid E. Scheffer,Leanne M. Dibbens +27 more
TL;DR: Findings show that mutations in PRRT2 cause both epilepsy and a movement disorder, and elicit pleiotropy in terms of both age of expression and anatomical substrate (cortex versus basal ganglia).
Journal ArticleDOI
Early onset epileptic encephalopathy caused by de novo SCN8A mutations.
Chihiro Ohba,Mitsuhiro Kato,Satoru Takahashi,Tally Lerman-Sagie,Dorit Lev,Hiroshi Terashima,Masaya Kubota,Hisashi Kawawaki,Mayumi Matsufuji,Yasuko Kojima,Akihiko Tateno,Hadassa Goldberg-Stern,Rachel Straussberg,Dafna Marom,Esther Leshinsky-Silver,Mitsuko Nakashima,Kiyomi Nishiyama,Yoshinori Tsurusaki,Noriko Miyake,Fumiaki Tanaka,Naomichi Matsumoto,Hirotomo Saitsu +21 more
TL;DR: Seven patients with de novo heterozygous SCN8A mutations, which were found in the comprehensive genetic analysis for early onset epileptic encephalopathies (EOEEs), are reported.
Journal ArticleDOI
Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.
Xianhua Piao,Bernard S. Chang,Adria Bodell,Katelyn Woods,Bruria Ben-Zeev,Meral Topçu,Renzo Guerrini,Hadassa Goldberg-Stern,László Sztriha,William B. Dobyns,A. James Barkovich,Christopher A. Walsh +11 more
TL;DR: This study provides a molecular confirmation of the BFPP phenotype and provides the wherewithal for diagnostic screening.
Journal ArticleDOI
Attention-deficit disorders and epilepsy in childhood: incidence, causative relations and treatment possibilities.
TL;DR: Methylphenidate is considered safe for use in children who are seizure-free and the few reports of seizure aggravation in methylphenidate-treated children with uncontrolled epilepsy have raised concern.
Journal ArticleDOI
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
Todor Arsov,Saul A. Mullen,Saul A. Mullen,Sue Rogers,A. Marie Phillips,Kate M. Lawrence,John A. Damiano,Hadassa Goldberg-Stern,Zaid Afawi,Sara Kivity,Chantal Trager,Steven Petrou,Steven Petrou,Samuel F. Berkovic,Ingrid E. Scheffer,Ingrid E. Scheffer,Ingrid E. Scheffer +16 more
TL;DR: This work examined whether glucose transporter 1 (GLUT1) deficiency causes common idiopathic generalized epilepsies (IGEs) and found no evidence that either cause or contribute to IGEs.