Hadassah Stern-Goldberg

Petah Tiqwa, M 49202, Israel

Last Updated: 09/26/2026

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Found 16 publications

Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.

Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.

Journal: Epilepsia

Published: December 29, 2021

Corrigendum to "Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?" [Seizure 79 (2020) 86-89].

Corrigendum to "Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?" [Seizure 79 (2020) 86-89].

Journal: Seizure

Published: November 27, 2020

Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years.

Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years.

Journal: Neuropediatrics

Published: July 07, 2020

Widespread cortical dyslamination in epilepsy patients with malformations of cortical development.

Widespread cortical dyslamination in epilepsy patients with malformations of cortical development.

Journal: Neuroradiology

Published: June 11, 2020

Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect the diagnostic yield?

Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect the diagnostic yield?

Journal: Seizure

Published: November 07, 2019

Dual array EEG-fMRI: An approach for motion artifact suppression in EEG recorded simultaneously with fMRI.

Dual array EEG-fMRI: An approach for motion artifact suppression in EEG recorded simultaneously with fMRI.

Journal: NeuroImage

Published: December 17, 2015

Lethal neonatal rigidity and multifocal seizure syndrome--report of another family with a BRAT1 mutation.

Lethal neonatal rigidity and multifocal seizure syndrome--report of another family with a BRAT1 mutation.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: October 23, 2014

Hyperventilation during routine electroencephalography: are three minutes really necessary?

Hyperventilation during routine electroencephalography: are three minutes really necessary?

Journal: Pediatric neurology

Published: September 27, 2014

Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22.

Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: January 20, 2014

Sensitivity and specificity of seizure-onset zone estimation by ictal magnetoencephalography.

Sensitivity and specificity of seizure-onset zone estimation by ictal magnetoencephalography.

Journal: Epilepsia

Published: July 12, 2012

Effect of melatonin on seizure frequency in intractable epilepsy: a pilot study.

Effect of melatonin on seizure frequency in intractable epilepsy: a pilot study.

Journal: Journal of child neurology

Published: March 02, 2012

Immunoglobulin treatment for severe childhood epilepsy.

Immunoglobulin treatment for severe childhood epilepsy.

Journal: Pediatric neurology

Published: December 27, 2011

Showing 1-12 of 16

Last Updated: 09/26/2026